Galnt1 Variant Search Result - Rat Genome Database

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156296375	CV2236536	single nucleotide variant	NM_020474.4(GALNT1):c.149C>T (p.Pro50Leu)	not specified [RCV004110533]	uncertain significance	18	35663637	35663637	Human		name
329356513	CV2430786	single nucleotide variant	NM_020474.4(GALNT1):c.156A>C (p.Gln52His)	not specified [RCV004253963]	uncertain significance	18	35663644	35663644	Human		name
598158832	CV3977593	single nucleotide variant	NM_020474.4(GALNT1):c.101G>A (p.Cys34Tyr)	not specified [RCV005328141]	uncertain significance	18	35654763	35654763	Human		name
15159375	CV715953	single nucleotide variant	NM_020474.4(GALNT1):c.1440C>T (p.Asp480=)	not provided [RCV000969697]	benign	18	35703550	35703550	Human		name
156063063	CV2330981	single nucleotide variant	NM_020474.4(GALNT1):c.811C>G (p.Pro271Ala)	not specified [RCV004188023]	uncertain significance	18	35687137	35687137	Human		name
401892321	CV2777423	single nucleotide variant	NM_020474.4(GALNT1):c.497C>T (p.Pro166Leu)	not specified [RCV004356205]	uncertain significance	18	35683406	35683406	Human		name
597779684	CV3673531	single nucleotide variant	NM_020474.4(GALNT1):c.557G>A (p.Arg186His)	not specified [RCV004930443]	uncertain significance	18	35683466	35683466	Human		name
598202631	CV3977592	single nucleotide variant	NM_020474.4(GALNT1):c.439A>G (p.Met147Val)	not specified [RCV005337133]	uncertain significance	18	35677715	35677715	Human		name
598202636	CV3977594	single nucleotide variant	NM_020474.4(GALNT1):c.992G>A (p.Gly331Glu)	not specified [RCV005337134]	uncertain significance	18	35691025	35691025	Human		name
407486721	CV3436195	single nucleotide variant	NM_020474.4(GALNT1):c.1277G>A (p.Arg426His)	not specified [RCV004619168]	uncertain significance	18	35692298	35692298	Human		name
597779680	CV3673530	single nucleotide variant	NM_020474.4(GALNT1):c.1381G>A (p.Gly461Ser)	not specified [RCV004930442]	uncertain significance	18	35702978	35702978	Human		name
597779689	CV3673532	single nucleotide variant	NM_020474.4(GALNT1):c.1147A>G (p.Ile383Val)	not specified [RCV004930444]	uncertain significance	18	35691180	35691180	Human		name
155695701	CV1793937	single nucleotide variant	NM_024642.5(GALNT12):c.-3C>A	not specified [RCV004050583]	uncertain significance	9	98807696	98807696	Human		name
155696470	CV1800733	single nucleotide variant	NM_024642.5(GALNT12):c.-5G>A	not specified [RCV004052557]	uncertain significance	9	98807694	98807694	Human		name
401862171	CV2760609	single nucleotide variant	NM_024642.5(GALNT12):c.-1C>T	not specified [RCV004334258]	uncertain significance	9	98807698	98807698	Human		name
405263163	CV3189424	single nucleotide variant	NM_024642.5(GALNT12):c.-9G>A	GALNT12-related disorder [RCV003896658]	likely benign	9	98807690	98807690	Human		name , trait , alternate_id
405682712	CV3387712	single nucleotide variant	NM_024642.5(GALNT12):c.-2G>A	not specified [RCV004517688]	uncertain significance	9	98807697	98807697	Human		name
597684346	CV3731204	single nucleotide variant	NM_024642.5(GALNT12):c.*9G>A	Colorectal cancer, susceptibility to, 1 [RCV005358175]\|not provided [RCV004999036]	likely benign\|uncertain significance	9	98849101	98849101	Human	1	name
598205317	CV3896815	single nucleotide variant	NM_024642.5(GALNT12):c.-4G>A	Colorectal cancer, susceptibility to, 1 [RCV005356992]	uncertain significance	9	98807695	98807695	Human	1	name
150449597	CV1260842	single nucleotide variant	NM_024642.5(GALNT12):c.*67A>T	not provided [RCV001680511]	benign	9	98849159	98849159	Human		name
405290719	CV3197118	single nucleotide variant	NM_024642.5(GALNT12):c.-10T>C	GALNT12-related disorder [RCV003984680]	likely benign	9	98807689	98807689	Human		name , trait , alternate_id
597684415	CV3731209	single nucleotide variant	NM_024642.5(GALNT12):c.*10T>C	not provided [RCV004999041]	uncertain significance	9	98849102	98849102	Human		name
598158519	CV3896813	single nucleotide variant	NM_024642.5(GALNT12):c.-14C>T	Colorectal cancer, susceptibility to, 1 [RCV005367878]	uncertain significance	9	98807685	98807685	Human	1	name
598205309	CV3896814	single nucleotide variant	NM_024642.5(GALNT12):c.-15G>A	Colorectal cancer, susceptibility to, 1 [RCV005356991]	uncertain significance	9	98807684	98807684	Human	1	name
150502081	CV1255197	single nucleotide variant	NM_024642.5(GALNT12):c.*171A>G	not provided [RCV001677116]	benign	9	98849263	98849263	Human		name
126772149	CV1008805	single nucleotide variant	NM_024642.5(GALNT12):c.371+3G>A	not provided [RCV001323581]	uncertain significance	9	98808072	98808072	Human		name
126913229	CV1046345	single nucleotide variant	NM_024642.5(GALNT12):c.917+6G>A	not provided [RCV001370024]	uncertain significance	9	98831963	98831963	Human		name
155665232	CV1786743	single nucleotide variant	NM_024642.5(GALNT12):c.372-4G>T	not specified [RCV004049771]	likely benign\|uncertain significance	9	98823252	98823252	Human		name
155667022	CV1803128	single nucleotide variant	NM_024642.5(GALNT12):c.541+3G>T	not specified [RCV004053039]	uncertain significance	9	98823428	98823428	Human		name
155716716	CV1822776	single nucleotide variant	NM_024642.5(GALNT12):c.731+3A>G	not specified [RCV004055882]	uncertain significance	9	98826944	98826944	Human		name
155716719	CV1822777	single nucleotide variant	NM_024642.5(GALNT12):c.731+5G>A	not specified [RCV004055883]	uncertain significance	9	98826946	98826946	Human		name
11347848	CV240714	single nucleotide variant	NM_024642.5(GALNT12):c.917+9C>T	not provided [RCV000233522]	likely benign	9	98831966	98831966	Human		name
401784138	CV2721080	single nucleotide variant	NM_024642.5(GALNT12):c.732-5T>G	not provided [RCV003575067]\|not specified [RCV004328337]	uncertain significance	9	98831767	98831767	Human		name
401941370	CV2835920	deletion	NM_024642.5(GALNT12):c.731+1del	Colorectal cancer, susceptibility to, 1 [RCV003461630]	uncertain significance	9	98826941	98826941	Human	1	name
401942824	CV2835930	single nucleotide variant	NM_024642.5(GALNT12):c.917+5G>A	Colorectal cancer, susceptibility to, 1 [RCV003468242]	uncertain significance	9	98831962	98831962	Human	1	name
405245629	CV3051637	single nucleotide variant	NM_024642.5(GALNT12):c.542-2A>G	not provided [RCV003720361]	uncertain significance	9	98826750	98826750	Human		name
405134932	CV3163942	single nucleotide variant	NM_024642.5(GALNT12):c.372-3C>T	not provided [RCV003854930]	uncertain significance	9	98823253	98823253	Human		name
405682825	CV3387740	single nucleotide variant	NM_024642.5(GALNT12):c.918-3T>A	not specified [RCV004517716]	uncertain significance	9	98835246	98835246	Human		name
598219438	CV3895659	single nucleotide variant	NM_024642.5(GALNT12):c.731+8A>G	Colorectal cancer, susceptibility to, 1 [RCV005360499]	uncertain significance	9	98826949	98826949	Human	1	name
12897073	CV397042	single nucleotide variant	NM_024642.5(GALNT12):c.372-7T>A	Colorectal cancer, susceptibility to, 1 [RCV005355910]\|Hereditary cancer-predisposing syndrome [RCV005055016]\|not provided [RCV000457020]\|not specified [RCV002475919]	benign\|likely benign	9	98823249	98823249	Human	2	name
14710598	CV652077	single nucleotide variant	NM_024642.5(GALNT12):c.731+4C>T	GALNT12-related disorder [RCV003975332]\|not provided [RCV000815083]\|not specified [RCV004028838]	likely benign\|uncertain significance	9	98826945	98826945	Human	1	name , alternate_id
15097770	CV689966	single nucleotide variant	NM_024642.5(GALNT12):c.541+9C>T	Colorectal cancer, susceptibility to, 1 [RCV005367606]\|not provided [RCV000869532]	likely benign	9	98823434	98823434	Human	1	name
15136693	CV689967	single nucleotide variant	NM_024642.5(GALNT12):c.732-8G>T	not provided [RCV000864536]	likely benign	9	98831764	98831764	Human		name
15160689	CV779236	single nucleotide variant	NM_022479.3(GALNT17):c.589+9G>A	not provided [RCV000969950]	benign	7	71388410	71388410	Human		name
25317322	CV815416	single nucleotide variant	NM_024642.5(GALNT12):c.372-5T>C	not provided [RCV001465841]\|not specified [RCV004030805]	likely benign\|uncertain significance	9	98823251	98823251	Human		name
25323521	CV815417	deletion	NM_024642.5(GALNT12):c.541+1del	not specified [RCV004030848]	uncertain significance	9	98823425	98823425	Human		name
25323556	CV815418	single nucleotide variant	NM_024642.5(GALNT12):c.542-4C>T	not provided [RCV002067671]\|not specified [RCV004030849]	likely benign\|uncertain significance	9	98826748	98826748	Human		name
25326151	CV815419	single nucleotide variant	NM_024642.5(GALNT12):c.732-2A>G	not specified [RCV004030882]	uncertain significance	9	98831770	98831770	Human		name
25314443	CV815420	single nucleotide variant	NM_024642.5(GALNT12):c.918-2A>C	Colorectal cancer, susceptibility to, 1 [RCV004569974]\|not provided [RCV002551813]\|not specified [RCV004030420]	uncertain significance	9	98835247	98835247	Human	1	name
127273007	CV1098478	single nucleotide variant	NM_024642.5(GALNT12):c.1606-4G>C	not provided [RCV001431507]	likely benign	9	98848948	98848948	Human		name
127296112	CV1120067	single nucleotide variant	NM_024642.5(GALNT12):c.1344+9G>A	not provided [RCV001459889]	likely benign	9	98840142	98840142	Human		name
127298251	CV1120068	single nucleotide variant	NM_024642.5(GALNT12):c.1345-7T>C	not provided [RCV001477861]	likely benign	9	98844089	98844089	Human		name
150506780	CV1258051	single nucleotide variant	NM_024642.5(GALNT12):c.372-94G>C	not provided [RCV001678268]	benign	9	98823162	98823162	Human		name
150498753	CV1282259	single nucleotide variant	NM_024642.5(GALNT12):c.541+74G>T	not provided [RCV001718073]	benign	9	98823499	98823499	Human		name
150479832	CV1282400	single nucleotide variant	NM_024642.5(GALNT12):c.917+24C>T	not provided [RCV001714531]	benign	9	98831981	98831981	Human		name
151874565	CV1343417	single nucleotide variant	NM_024642.5(GALNT12):c.1344+4A>C	not provided [RCV001940230]\|not specified [RCV004043313]	uncertain significance	9	98840137	98840137	Human		name
151843469	CV1418469	single nucleotide variant	NM_024642.5(GALNT12):c.1035+1G>T	not provided [RCV001903134]	uncertain significance	9	98835367	98835367	Human		name
152068208	CV1547684	single nucleotide variant	NM_024642.5(GALNT12):c.541+19T>A	not provided [RCV002074737]	likely benign	9	98823444	98823444	Human		name
152138437	CV1549527	single nucleotide variant	NM_024642.5(GALNT12):c.1459-8A>G	not provided [RCV002156441]	likely benign	9	98845969	98845969	Human		name
152149839	CV1555787	single nucleotide variant	NM_024642.5(GALNT12):c.731+11C>T	not provided [RCV002179276]	likely benign	9	98826952	98826952	Human		name
152129071	CV1583839	single nucleotide variant	NM_024642.5(GALNT12):c.372-14C>T	Colorectal cancer, susceptibility to, 1 [RCV005361985]\|not provided [RCV002199079]	benign\|likely benign	9	98823242	98823242	Human	1	name
152079288	CV1596830	single nucleotide variant	NM_024642.5(GALNT12):c.731+12G>A	not provided [RCV002092635]	likely benign	9	98826953	98826953	Human		name
152123127	CV1603106	single nucleotide variant	NM_024642.5(GALNT12):c.917+10T>A	not provided [RCV002198324]	likely benign	9	98831967	98831967	Human		name
152089396	CV1639066	single nucleotide variant	NM_024642.5(GALNT12):c.541+11G>A	not provided [RCV002150391]	likely benign	9	98823436	98823436	Human		name
152032868	CV1643199	single nucleotide variant	NM_024642.5(GALNT12):c.542-13T>C	not provided [RCV002205062]	likely benign	9	98826739	98826739	Human		name
155687759	CV1803712	single nucleotide variant	NM_024642.5(GALNT12):c.1212+1G>T	not provided [RCV003730108]\|not specified [RCV004054286]	uncertain significance	9	98837149	98837149	Human		name
155691248	CV1827000	single nucleotide variant	NM_024642.5(GALNT12):c.1036-3C>T	not provided [RCV003095160]\|not specified [RCV004057829]	uncertain significance	9	98836969	98836969	Human		name
155677413	CV1829549	single nucleotide variant	NM_024642.5(GALNT12):c.1345-4T>G	not specified [RCV004058751]	uncertain significance	9	98844092	98844092	Human		name
155688652	CV1829972	single nucleotide variant	NM_024642.5(GALNT12):c.1035+1G>A	not specified [RCV004057217]	uncertain significance	9	98835367	98835367	Human		name
155730748	CV1837507	single nucleotide variant	NM_024642.5(GALNT12):c.1606-2A>G	not specified [RCV004057441]	uncertain significance	9	98848950	98848950	Human		name
156295955	CV1894265	deletion	NM_024642.5(GALNT12):c.732-15del	not provided [RCV003087693]	likely benign	9	98831757	98831757	Human		name
156152830	CV2100379	single nucleotide variant	NM_024642.5(GALNT12):c.731+14C>A	not provided [RCV002872381]	likely benign	9	98826955	98826955	Human		name
156206859	CV2110318	single nucleotide variant	NM_024642.5(GALNT12):c.372-13G>A	Colorectal cancer, susceptibility to, 1 [RCV005356224]\|not provided [RCV002957591]	likely benign	9	98823243	98823243	Human	1	name
156384107	CV2128282	single nucleotide variant	NM_024642.5(GALNT12):c.541+20C>G	not provided [RCV002943361]	likely benign	9	98823445	98823445	Human		name
401941371	CV2835922	single nucleotide variant	NM_024642.5(GALNT12):c.732-39T>A	Colorectal cancer, susceptibility to, 1 [RCV003461631]	uncertain significance	9	98831733	98831733	Human	1	name
401962182	CV2842985	single nucleotide variant	NM_024642.5(GALNT12):c.1036-1G>A	not provided [RCV003477241]	uncertain significance	9	98836971	98836971	Human		name
401962183	CV2842986	single nucleotide variant	NM_024642.5(GALNT12):c.1036-1G>T	not provided [RCV003477242]	uncertain significance	9	98836971	98836971	Human		name
405090684	CV2859345	single nucleotide variant	NM_024642.5(GALNT12):c.542-16T>C	not provided [RCV003549847]	likely benign	9	98826736	98826736	Human		name
405071402	CV2944269	single nucleotide variant	NM_024642.5(GALNT12):c.731+19A>G	not provided [RCV003659444]	likely benign	9	98826960	98826960	Human		name
405143998	CV2946075	duplication	NM_024642.5(GALNT12):c.542-11dup	not provided [RCV003669509]	likely benign	9	98826738	98826739	Human		name
405020400	CV2992623	single nucleotide variant	NM_024642.5(GALNT12):c.371+19G>A	not provided [RCV003694775]	likely benign	9	98808088	98808088	Human		name
405150761	CV3031333	single nucleotide variant	NM_024642.5(GALNT12):c.1606-9C>G	not provided [RCV003703278]	likely benign	9	98848943	98848943	Human		name
405252272	CV3047106	single nucleotide variant	NM_024642.5(GALNT12):c.918-18G>A	not provided [RCV003722146]	likely benign	9	98835231	98835231	Human		name
405868883	CV3400644	single nucleotide variant	NM_024642.5(GALNT12):c.1212+1G>A	Colorectal cancer, susceptibility to, 1 [RCV004576647]	uncertain significance	9	98837149	98837149	Human	1	name
597779810	CV3673614	single nucleotide variant	NM_024642.5(GALNT12):c.1606-5T>G	not specified [RCV004930473]	uncertain significance	9	98848947	98848947	Human		name
597870452	CV3749917	single nucleotide variant	NM_024642.5(GALNT12):c.541+10G>A	not provided [RCV005068598]	likely benign	9	98823435	98823435	Human		name
597935038	CV3759358	single nucleotide variant	NM_024642.5(GALNT12):c.1212+3G>C	not provided [RCV005076478]	uncertain significance	9	98837151	98837151	Human		name
12897930	CV397062	single nucleotide variant	NM_024642.5(GALNT12):c.1605+4G>A	Colorectal cancer, susceptibility to, 1 [RCV002489130]\|not provided [RCV000469507]\|not specified [RCV002475922]	benign\|likely benign	9	98846127	98846127	Human	1	name
14711385	CV651946	duplication	NM_024642.5(GALNT12):c.1035+2dup	not provided [RCV000817586]	uncertain significance	9	98835367	98835368	Human		name
14706034	CV651989	single nucleotide variant	NM_024642.5(GALNT12):c.1213-3C>T	not provided [RCV000802846]\|not specified [RCV004028122]	uncertain significance	9	98839999	98839999	Human		name
15135554	CV689968	single nucleotide variant	NM_024642.5(GALNT12):c.1345-9T>C	not provided [RCV000864336]	likely benign	9	98844087	98844087	Human		name
15188516	CV777839	single nucleotide variant	NM_024642.5(GALNT12):c.1035+7A>G	not provided [RCV000953901]	likely benign	9	98835373	98835373	Human		name
15128901	CV778935	single nucleotide variant	NM_024572.4(GALNT14):c.533-10C>T	not provided [RCV000964165]	benign	2	30955749	30955749	Human		name
126750653	CV993630	single nucleotide variant	NM_024642.5(GALNT12):c.1458+7A>G	not provided [RCV001297365]	likely benign\|uncertain significance	9	98844216	98844216	Human		name
127309152	CV1120069	single nucleotide variant	NM_024642.5(GALNT12):c.1606-10T>C	not provided [RCV001463508]	likely benign	9	98848942	98848942	Human		name
150501474	CV1223714	single nucleotide variant	NM_024642.5(GALNT12):c.732-171T>G	not provided [RCV001620835]	benign	9	98831601	98831601	Human		name
150493968	CV1226067	single nucleotide variant	NM_024642.5(GALNT12):c.732-229T>C	not provided [RCV001619285]	benign	9	98831543	98831543	Human		name
150508804	CV1244922	single nucleotide variant	NM_024642.5(GALNT12):c.542-304T>G	not provided [RCV001659173]	benign	9	98826448	98826448	Human		name
150460838	CV1253165	deletion	NM_024642.5(GALNT12):c.1036-42del	not provided [RCV001669494]	benign	9	98836930	98836930	Human		name
150467023	CV1255837	single nucleotide variant	NM_024642.5(GALNT12):c.1344+61G>T	not provided [RCV001670471]	benign	9	98840194	98840194	Human		name
150437252	CV1262275	single nucleotide variant	NM_024642.5(GALNT12):c.541+285G>A	not provided [RCV001678633]	benign	9	98823710	98823710	Human		name
150467051	CV1268876	single nucleotide variant	NM_024642.5(GALNT12):c.918-263A>C	not provided [RCV001694573]	benign	9	98834986	98834986	Human		name
150493837	CV1282251	single nucleotide variant	NM_024642.5(GALNT12):c.541+124C>T	not provided [RCV001717088]	benign	9	98823549	98823549	Human		name
150498747	CV1282258	single nucleotide variant	NM_024642.5(GALNT12):c.1458+58G>T	not provided [RCV001718072]	benign	9	98844267	98844267	Human		name
150539442	CV1308825	single nucleotide variant	NM_024642.5(GALNT12):c.371+130A>T	not provided [RCV001766329]	likely benign	9	98808199	98808199	Human		name
151773004	CV1504835	single nucleotide variant	NM_024642.5(GALNT12):c.1212+12G>A	not provided [RCV001988422]	likely benign	9	98837160	98837160	Human		name
152043870	CV1534339	single nucleotide variant	NM_024642.5(GALNT12):c.1459-19T>G	not provided [RCV002088316]	likely benign	9	98845958	98845958	Human		name
152041500	CV1555925	single nucleotide variant	NM_024642.5(GALNT12):c.1036-13T>C	not provided [RCV002188323]	likely benign	9	98836959	98836959	Human		name
152083139	CV1565192	single nucleotide variant	NM_024642.5(GALNT12):c.1035+19T>C	not provided [RCV002093117]	likely benign	9	98835385	98835385	Human		name
152167227	CV1577392	single nucleotide variant	NM_024642.5(GALNT12):c.1458+12C>G	not provided [RCV002204653]	likely benign	9	98844221	98844221	Human		name
152086911	CV1601079	single nucleotide variant	NM_024642.5(GALNT12):c.1212+15C>T	Colorectal cancer, susceptibility to, 1 [RCV005361955]\|not provided [RCV002093610]	likely benign	9	98837163	98837163	Human	1	name
152057189	CV1647385	single nucleotide variant	NM_024642.5(GALNT12):c.1213-14T>C	not provided [RCV002208236]	likely benign	9	98839988	98839988	Human		name
152124561	CV1665693	single nucleotide variant	NM_024642.5(GALNT12):c.1036-15T>C	not provided [RCV002198506]	likely benign	9	98836957	98836957	Human		name
156390245	CV2122409	single nucleotide variant	NM_024642.5(GALNT12):c.1345-18C>T	not provided [RCV002943824]	likely benign	9	98844078	98844078	Human		name
11050185	CV225531	single nucleotide variant	NM_024642.5(GALNT12):c.1036-27C>T	Hereditary cancer-predisposing syndrome [RCV000209769]	likely benign	9	98836945	98836945	Human	1	name
405196350	CV2868962	single nucleotide variant	NM_024642.5(GALNT12):c.1458+20G>C	not provided [RCV003550874]	likely benign	9	98844229	98844229	Human		name
405147945	CV2881777	single nucleotide variant	NM_024642.5(GALNT12):c.1212+18C>T	not provided [RCV003561509]	likely benign	9	98837166	98837166	Human		name
402470563	CV2927976	single nucleotide variant	NM_024642.5(GALNT12):c.1458+20G>A	not provided [RCV003570322]	likely benign	9	98844229	98844229	Human		name
405176434	CV2951854	single nucleotide variant	NM_024642.5(GALNT12):c.1212+11C>T	not provided [RCV003675809]	likely benign	9	98837159	98837159	Human		name
405140873	CV2962021	single nucleotide variant	NM_024642.5(GALNT12):c.1458+16A>G	not provided [RCV003673211]	likely benign	9	98844225	98844225	Human		name
405136832	CV2963167	deletion	NM_024642.5(GALNT12):c.1035+11del	not provided [RCV003668860]	likely benign	9	98835377	98835377	Human		name
402492208	CV3011894	single nucleotide variant	NM_024642.5(GALNT12):c.1459-10C>A	not provided [RCV003687543]	uncertain significance	9	98845967	98845967	Human		name
26896956	CV851760	single nucleotide variant	NM_024642.5(GALNT12):c.1213-10G>T	GALNT12-related disorder [RCV003963029]\|not provided [RCV001065012]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	9	98839992	98839992	Human	1	name , alternate_id
40814938	CV970175	single nucleotide variant	NM_198321.4(GALNT10):c.263-139G>C	not provided [RCV004706079]\|not specified [RCV001261640]	benign\|likely benign	5	154297802	154297802	Human		name
40814940	CV970176	single nucleotide variant	NM_198321.4(GALNT10):c.263-138A>T	not provided [RCV004706080]\|not specified [RCV001261641]	benign\|likely benign	5	154297803	154297803	Human		name
8576680	CV111048	single nucleotide variant	NM_052917.3(GALNT13):c.311+6476A>T	Lung cancer [RCV000091571]	uncertain significance	2	154146981	154146981	Human		name
150460986	CV1215749	single nucleotide variant	NM_024642.5(GALNT12):c.1458+189C>T	not provided [RCV001613451]	benign	9	98844398	98844398	Human		name
150473644	CV1217664	single nucleotide variant	NM_024642.5(GALNT12):c.1459-216G>A	not provided [RCV001615675]	benign	9	98845761	98845761	Human		name
150469218	CV1219037	single nucleotide variant	NM_024642.5(GALNT12):c.1459-105T>A	not provided [RCV001614789]	benign	9	98845872	98845872	Human		name
150511221	CV1242645	single nucleotide variant	NM_024642.5(GALNT12):c.1459-327T>A	not provided [RCV001660997]	benign	9	98845650	98845650	Human		name
150447907	CV1261885	single nucleotide variant	NM_024642.5(GALNT12):c.1036-204A>G	not provided [RCV001680270]	benign	9	98836768	98836768	Human		name
150452611	CV1276748	duplication	NM_024642.5(GALNT12):c.1344+135dup	not provided [RCV001708538]	benign	9	98840262	98840263	Human		name
150471223	CV1280930	single nucleotide variant	NM_024642.5(GALNT12):c.1459-234C>A	not provided [RCV001713143]	benign	9	98845743	98845743	Human		name
150479378	CV1282254	single nucleotide variant	NM_024642.5(GALNT12):c.1212+128A>T	not provided [RCV001714456]	benign	9	98837276	98837276	Human		name
150493841	CV1282255	single nucleotide variant	NM_024642.5(GALNT12):c.1212+178C>G	not provided [RCV001717089]	benign	9	98837326	98837326	Human		name
150498743	CV1282257	single nucleotide variant	NM_024642.5(GALNT12):c.1213-113C>G	not provided [RCV001718071]	benign	9	98839889	98839889	Human		name
11049882	CV225532	single nucleotide variant	NM_024642.5(GALNT12):c.371+1744G>T	Hereditary cancer-predisposing syndrome [RCV000209141]	likely benign	9	98809813	98809813	Human	1	name
8576678	CV111046	single nucleotide variant	NM_052917.3(GALNT13):c.143-87014G>C	Lung cancer [RCV000091569]	uncertain significance	2	154053323	154053323	Human		name
8576679	CV111047	single nucleotide variant	NM_052917.3(GALNT13):c.143-84048G>C	Lung cancer [RCV000091570]	uncertain significance	2	154056289	154056289	Human		name
8576681	CV111049	single nucleotide variant	NM_052917.3(GALNT13):c.311+14801G>A	Lung cancer [RCV000091572]	uncertain significance	2	154155306	154155306	Human		name
8576682	CV111050	single nucleotide variant	NM_052917.3(GALNT13):c.1156+5244T>A	Lung cancer [RCV000091573]	uncertain significance	2	154306833	154306833	Human		name
8576683	CV111051	single nucleotide variant	NM_052917.3(GALNT13):c.1396-4944G>C	Lung cancer [RCV000091574]	uncertain significance	2	154433648	154433648	Human		name
8580451	CV114881	single nucleotide variant	NM_198321.3(GALNT10):c.569-10665C>G	Lung cancer [RCV000095404]	uncertain significance	5	154365612	154365612	Human		name
8590615	CV125307	single nucleotide variant	NM_022087.3(GALNT11):c.-38-19450A>G	Lung cancer [RCV000105826]	uncertain significance	7	152074740	152074740	Human		name
8652554	CV129129	single nucleotide variant	NM_198516.2(GALNT18):c.595+18722G>A	Lung cancer [RCV000109616]	uncertain significance	11	11413899	11413899	Human		name
151797538	CV1467737	duplication	NM_024642.5(GALNT12):c.732-4_771dup	not provided [RCV001952614]\|not specified [RCV004041985]	uncertain significance	9	98831765	98831766	Human		name
25318170	CV815415	indel	NM_024642.5(GALNT12):c.-4_-3delinsA	not specified [RCV004030808]	uncertain significance	9	98807695	98807696	Human		name
8630317	CV85472	single nucleotide variant	NM_024572.3(GALNT14):c.129+23156C>T	Malignant melanoma [RCV000065555]	not provided	2	31114802	31114802	Human		name
8577111	CV111481	single nucleotide variant	NM_001253826.1(GALNT14):c.843-1115A>T	Lung cancer [RCV000092004]	uncertain significance	2	30943419	30943419	Human		name
329367272	CV2438896	deletion	NM_024642.5(GALNT12):c.876_917+174del	not provided [RCV005101281]\|not specified [RCV004264426]	uncertain significance	9	98831915	98832130	Human		name
11542208	CV248499	deletion	NM_024642.4(GALNT12):c.732-?_1035+?del	not specified [RCV000240291]	uncertain significance				Human		name
151714371	CV1488457	deletion	NM_024642.5(GALNT12):c.1035+4_1035+7del	not provided [RCV002002635]	uncertain significance	9	98835367	98835370	Human		name
151877086	CV1395362	duplication	NM_024642.5(GALNT12):c.1459-15_1459-1dup	GALNT12-related disorder [RCV003418311]\|not provided [RCV002019667]\|not specified [RCV004045926]	uncertain significance	9	98845960	98845961	Human	1	name , alternate_id
402519926	CV2902602	microsatellite	NM_024642.5(GALNT12):c.1213-10_1213-8del	not provided [RCV003575777]	likely benign	9	98839987	98839989	Human		name
152168417	CV1558698	deletion	NM_024642.5(GALNT12):c.1345-13_1345-12del	not provided [RCV002142438]	likely benign	9	98844082	98844083	Human		name
156094103	CV2139402	indel	NM_024642.5(GALNT12):c.1345-79_1364delinsTCAA	not provided [RCV002979724]	uncertain significance	9	98844017	98844115	Human		name
598199690	CV4007347	duplication	NM_052917.4(GALNT13):c.142+41082_142+41090dup	Zimmermann-laband syndrome 3 [RCV005398175]	uncertain significance	2	153985719	153985720	Human	1	name
598199696	CV4007348	duplication	NM_052917.4(GALNT13):c.142+41089_142+41091dup	Zimmermann-laband syndrome 3 [RCV005398176]	uncertain significance	2	153985725	153985726	Human	1	name
126773513	CV1029373	single nucleotide variant	NM_024642.5(GALNT12):c.1368C>A (p.Asp456Glu)	GALNT12-related disorder [RCV004731131]\|not provided [RCV001346227]\|not specified [RCV004036484]	uncertain significance	9	98844119	98844119	Human	1	alternate_id
151856871	CV1401946	single nucleotide variant	NM_024642.5(GALNT12):c.1676T>G (p.Phe559Cys)	GALNT12-related disorder [RCV003958466]\|not provided [RCV002017287]	uncertain significance	9	98849022	98849022	Human	1	alternate_id
155694167	CV1837524	single nucleotide variant	NM_024642.5(GALNT12):c.1606G>A (p.Asp536Asn)	Colorectal cancer, susceptibility to, 1 [RCV004572425]\|GALNT12-related disorder [RCV004753562]\|not provided [RCV005097632]\|not specified [RCV004057447]	uncertain significance	9	98848952	98848952	Human	1	alternate_id
10767517	CV221933	single nucleotide variant	NM_024642.5(GALNT12):c.566A>G (p.Asn189Ser)	Colorectal cancer, susceptibility to, 1 [RCV005049484]\|Familial colorectal cancer [RCV001824686]\|GALNT12-related disorder [RCV004752796]\|not provided [RCV000204844]\|not specified [RCV004020541]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance\|not provided	9	98826776	98826776	Human	1	alternate_id
10768351	CV221935	single nucleotide variant	NM_024642.5(GALNT12):c.1392C>G (p.Pro464=)	Colorectal cancer, susceptibility to, 1 [RCV005396651]\|GALNT12-related disorder [RCV003917844]\|not provided [RCV000206253]\|not specified [RCV002478737]	benign\|likely benign	9	98844143	98844143	Human	1	name , alternate_id
11050219	CV226331	single nucleotide variant	NM_024642.5(GALNT12):c.907G>A (p.Asp303Asn)	Adenomatous polyposis coli, attenuated [RCV000656380]\|Colorectal cancer, susceptibility to, 1 [RCV005396681]\|GALNT12-related disorder [RCV003937792]\|Hereditary cancer-predisposing syndrome [RCV000210098]\|not provided [RCV000229689]\|not specified [RCV004020573]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	9	98831947	98831947	Human	3	alternate_id
11346533	CV240704	single nucleotide variant	NM_024642.5(GALNT12):c.20G>T (p.Arg7Leu)	GALNT12-related disorder [RCV004752810]\|not provided [RCV001396556]\|not specified [RCV004020877]	benign\|likely benign\|uncertain significance	9	98807718	98807718	Human	1	name , alternate_id
11348747	CV240705	indel	NM_024642.5(GALNT12):c.136_138delinsAGA (p.Gly46Arg)	Colorectal cancer, susceptibility to, 1 [RCV005396818]\|GALNT12-related disorder [RCV003897564]\|not provided [RCV003477835]\|not specified [RCV000227879]	likely benign\|uncertain significance	9	98807834	98807836	Human		alternate_id
11349677	CV240712	single nucleotide variant	NM_024642.5(GALNT12):c.889C>T (p.Arg297Trp)	Colorectal cancer, susceptibility to, 1 [RCV003463683]\|GALNT12-related disorder [RCV003907894]\|not provided [RCV000231446]\|not specified [RCV004020880]	conflicting interpretations of pathogenicity\|uncertain significance	9	98831929	98831929	Human	1	alternate_id
11345944	CV240713	single nucleotide variant	NM_024642.5(GALNT12):c.890G>A (p.Arg297Gln)	Colorectal cancer, susceptibility to, 1 [RCV004567759]\|GALNT12-related disorder [RCV004752811]\|not provided [RCV000226829]\|not specified [RCV004020881]	uncertain significance	9	98831930	98831930	Human	1	alternate_id
401856991	CV2759917	single nucleotide variant	NM_024642.5(GALNT12):c.228C>A (p.Gly76=)	GALNT12-related disorder [RCV003966333]\|not specified [RCV004345343]	likely benign	9	98807926	98807926	Human	1	name , alternate_id
401919771	CV2798394	single nucleotide variant	NM_024642.5(GALNT12):c.1562G>A (p.Cys521Tyr)	GALNT12-related disorder [RCV003402359]	uncertain significance	9	98846080	98846080	Human		trait , alternate_id
405255956	CV3208436	single nucleotide variant	NM_198321.4(GALNT10):c.1356C>T (p.Pro452=)	GALNT10-related disorder [RCV003939534]	likely benign	5	154409732	154409732	Human		name , trait , alternate_id
405285503	CV3212525	single nucleotide variant	NM_024572.4(GALNT14):c.1599C>G (p.Ile533Met)	GALNT14-related disorder [RCV003959107]	uncertain significance	2	30910961	30910961	Human		trait , alternate_id
405258825	CV3215161	single nucleotide variant	NM_024572.4(GALNT14):c.976G>A (p.Val326Ile)	GALNT14-related disorder [RCV003942208]	likely benign	2	30932150	30932150	Human		trait , alternate_id
408384559	CV3504320	single nucleotide variant	NM_024572.4(GALNT14):c.1382T>A (p.Val461Glu)	GALNT14-related disorder [RCV004731915]	uncertain significance	2	30912341	30912341	Human		trait , alternate_id
408384333	CV3505092	single nucleotide variant	NM_198321.4(GALNT10):c.1201T>G (p.Tyr401Asp)	GALNT10-related disorder [RCV004731723]	uncertain significance	5	154409577	154409577	Human		trait , alternate_id
12897568	CV397041	single nucleotide variant	NM_024642.5(GALNT12):c.144C>G (p.Ala48=)	GALNT12-related disorder [RCV003902707]\|not provided [RCV000464320]\|not specified [RCV004023013]	likely benign	9	98807842	98807842	Human	1	name , alternate_id
12897541	CV397056	single nucleotide variant	NM_024642.5(GALNT12):c.719C>T (p.Pro240Leu)	Breast neoplasm [RCV001265633]\|Colorectal cancer, susceptibility to, 1 [RCV005398633]\|GALNT12-related disorder [RCV003970287]\|not provided [RCV000463956]\|not specified [RCV004022800]	benign\|likely benign\|uncertain significance	9	98826929	98826929	Human	3	alternate_id
12898333	CV397058	single nucleotide variant	NM_024642.5(GALNT12):c.840C>T (p.Asp280=)	Colorectal cancer, susceptibility to, 1 [RCV005398668]\|GALNT12-related disorder [RCV003942565]\|not provided [RCV000475487]\|not specified [RCV002475923]	benign\|likely benign	9	98831880	98831880	Human	1	name , alternate_id
12898202	CV397266	single nucleotide variant	NM_024642.5(GALNT12):c.303C>G (p.His101Gln)	GALNT12-related disorder [RCV003401483]\|not provided [RCV000473689]\|not specified [RCV004022792]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	9	98808001	98808001	Human	1	alternate_id
12897695	CV397272	single nucleotide variant	NM_024642.5(GALNT12):c.567T>C (p.Asn189=)	Colorectal cancer, susceptibility to, 1 [RCV005398662]\|GALNT12-related disorder [RCV003915312]\|not provided [RCV000466025]\|not specified [RCV004023010]	benign\|likely benign	9	98826777	98826777	Human	1	name , alternate_id
12897607	CV397275	single nucleotide variant	NM_024642.5(GALNT12):c.579A>G (p.Gly193=)	GALNT12-related disorder [RCV003925373]\|not provided [RCV000464914]\|not specified [RCV001821369]	benign\|likely benign	9	98826789	98826789	Human	1	name , alternate_id
12898094	CV397277	single nucleotide variant	NM_024642.5(GALNT12):c.606C>T (p.Ala202=)	GALNT12-related disorder [RCV004752907]\|not provided [RCV000471887]\|not specified [RCV004023009]	likely benign	9	98826816	98826816	Human	1	name , alternate_id
12897334	CV397279	single nucleotide variant	NM_024642.5(GALNT12):c.673A>T (p.Thr225Ser)	GALNT12-related disorder [RCV003942564]\|not provided [RCV000460711]\|not specified [RCV004023012]	benign\|likely benign\|uncertain significance	9	98826883	98826883	Human	1	alternate_id
12897520	CV397296	single nucleotide variant	NM_024642.5(GALNT12):c.1392C>T (p.Pro464=)	Colorectal cancer, susceptibility to, 1 [RCV005398669]\|GALNT12-related disorder [RCV003970348]\|not provided [RCV000463620]\|not specified [RCV004023018]	benign\|likely benign	9	98844143	98844143	Human	1	name , alternate_id
12897434	CV397601	single nucleotide variant	NM_024642.5(GALNT12):c.691T>C (p.Cys231Arg)	Colorectal cancer, susceptibility to, 1 [RCV004568059]\|GALNT12-related disorder [RCV003960036]\|not provided [RCV000462237]\|not specified [RCV004022802]	uncertain significance	9	98826901	98826901	Human	1	alternate_id
12898184	CV397606	single nucleotide variant	NM_024642.5(GALNT12):c.897A>G (p.Gln299=)	Colorectal cancer, susceptibility to, 1 [RCV005398664]\|GALNT12-related disorder [RCV003915313]\|Hereditary cancer-predisposing syndrome [RCV005055017]\|not provided [RCV000473367]\|not specified [RCV002475921]	benign	9	98831937	98831937	Human	2	name , alternate_id
13498935	CV474971	single nucleotide variant	NM_024642.5(GALNT12):c.136G>A (p.Gly46Arg)	Colorectal cancer, susceptibility to, 1 [RCV005398909]\|GALNT12-related disorder [RCV003925748]\|not provided [RCV000860775]\|not specified [RCV004024516]	benign\|likely benign	9	98807834	98807834	Human	1	name , alternate_id
13504092	CV475028	single nucleotide variant	NM_024642.5(GALNT12):c.909T>C (p.Asp303=)	GALNT12-related disorder [RCV004752950]\|not provided [RCV000869136]\|not specified [RCV004024519]	benign\|likely benign	9	98831949	98831949	Human	1	name , alternate_id
13489440	CV475035	single nucleotide variant	NM_024642.5(GALNT12):c.5G>T (p.Trp2Leu)	Colorectal cancer, susceptibility to, 1 [RCV004569270]\|GALNT12-related disorder [RCV004752951]\|not provided [RCV000821211]\|not specified [RCV004599222]	uncertain significance	9	98807703	98807703	Human	1	name , alternate_id
13496885	CV475046	single nucleotide variant	NM_024642.5(GALNT12):c.858G>A (p.Thr286=)	Colorectal cancer, susceptibility to, 1 [RCV005398913]\|GALNT12-related disorder [RCV003962636]\|not provided [RCV000867263]\|not specified [RCV004024533]	likely benign	9	98831898	98831898	Human	1	name , alternate_id
13473952	CV475182	single nucleotide variant	NM_024642.5(GALNT12):c.356A>T (p.Glu119Val)	Colorectal cancer, susceptibility to, 1 [RCV005398910]\|GALNT12-related disorder [RCV003980058]\|Hereditary cancer-predisposing syndrome [RCV005055018]\|not provided [RCV001510672]\|not specified [RCV004024517]	benign	9	98808054	98808054	Human	2	alternate_id
13470960	CV475231	single nucleotide variant	NM_024642.5(GALNT12):c.858G>T (p.Thr286=)	GALNT12-related disorder [RCV003900279]\|not provided [RCV000870245]\|not specified [RCV004024534]	likely benign	9	98831898	98831898	Human	1	name , alternate_id
13476209	CV475232	single nucleotide variant	NM_024642.5(GALNT12):c.1197C>T (p.Asn399=)	GALNT12-related disorder [RCV003900280]\|not provided [RCV000876935]\|not specified [RCV004024554]	likely benign	9	98837133	98837133	Human	1	name , alternate_id
15102938	CV687570	single nucleotide variant	NM_024642.5(GALNT12):c.321C>T (p.Leu107=)	GALNT12-related disorder [RCV003908265]\|not provided [RCV000870563]\|not specified [RCV004027779]	likely benign	9	98808019	98808019	Human	1	name , alternate_id
15147932	CV687575	single nucleotide variant	NM_024642.5(GALNT12):c.1563C>T (p.Cys521=)	GALNT12-related disorder [RCV003928388]\|not provided [RCV000866564]\|not specified [RCV004027674]	likely benign	9	98846081	98846081	Human	1	name , alternate_id
15116426	CV736036	single nucleotide variant	NM_022087.4(GALNT11):c.53C>T (p.Ala18Val)	GALNT11-related disorder [RCV003968179]\|not provided [RCV000895199]	likely benign	7	152094280	152094280	Human		name , alternate_id
25319554	CV809671	single nucleotide variant	NM_024642.5(GALNT12):c.43C>A (p.Arg15=)	GALNT12-related disorder [RCV003928666]\|not specified [RCV004030820]	likely benign	9	98807741	98807741	Human	1	name , alternate_id
155731355	CV1825942	single nucleotide variant	NM_024642.5(GALNT12):c.9G>T (p.Gly3=)	not specified [RCV004057766]	likely benign	9	98807707	98807707	Human		name
598202732	CV3977610	single nucleotide variant	NM_024642.5(GALNT12):c.9G>A (p.Gly3=)	not specified [RCV005337148]	likely benign	9	98807707	98807707	Human		name
152128738	CV1596599	single nucleotide variant	NM_024642.5(GALNT12):c.18G>T (p.Ala6=)	not provided [RCV002118796]\|not specified [RCV004917779]	likely benign	9	98807716	98807716	Human		name
155747701	CV1849710	single nucleotide variant	NM_024642.5(GALNT12):c.19C>A (p.Arg7=)	not specified [RCV004061723]	likely benign	9	98807717	98807717	Human		name
155689804	CV1850592	single nucleotide variant	NM_024642.5(GALNT12):c.21G>C (p.Arg7=)	not specified [RCV004061213]	likely benign	9	98807719	98807719	Human		name
329380103	CV2426400	single nucleotide variant	NM_024642.5(GALNT12):c.12C>T (p.Arg4=)	not specified [RCV004245090]	likely benign	9	98807710	98807710	Human		name
401941293	CV2835924	duplication	NM_024642.5(GALNT12):c.9dup (p.Arg4fs)	Colorectal cancer, susceptibility to, 1 [RCV003461633]\|not provided [RCV003779034]	uncertain significance	9	98807702	98807703	Human	1	name
597753756	CV3673570	single nucleotide variant	NM_024642.5(GALNT12):c.21G>A (p.Arg7=)	not specified [RCV004924211]	likely benign	9	98807719	98807719	Human		name
14738700	CV638614	single nucleotide variant	NM_024642.5(GALNT12):c.15G>A (p.Thr5=)	not provided [RCV000804637]\|not specified [RCV004028182]	likely benign\|uncertain significance	9	98807713	98807713	Human		name
15108754	CV767574	single nucleotide variant	NM_024642.5(GALNT12):c.27C>T (p.Arg9=)	not provided [RCV000938212]\|not specified [RCV004029669]	likely benign	9	98807725	98807725	Human		name
126915087	CV1046332	single nucleotide variant	NM_024642.5(GALNT12):c.5G>A (p.Trp2Ter)	not provided [RCV001370710]\|not specified [RCV004037478]	uncertain significance	9	98807703	98807703	Human		name
127272231	CV1076837	single nucleotide variant	NM_024642.5(GALNT12):c.33G>C (p.Pro11=)	not provided [RCV001405661]	likely benign	9	98807731	98807731	Human		name
127268841	CV1098474	single nucleotide variant	NM_024642.5(GALNT12):c.51C>A (p.Gly17=)	not provided [RCV001430111]\|not specified [RCV004038281]	likely benign	9	98807749	98807749	Human		name
127337752	CV1140890	single nucleotide variant	NM_024642.5(GALNT12):c.72C>T (p.Leu24=)	not provided [RCV001493037]\|not specified [RCV004037326]	likely benign	9	98807770	98807770	Human		name
150543915	CV1309872	single nucleotide variant	NM_024642.5(GALNT12):c.2T>C (p.Met1Thr)	not provided [RCV002540740]\|not specified [RCV004040752]	likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance	9	98807700	98807700	Human		name
151826019	CV1467214	single nucleotide variant	NM_024642.5(GALNT12):c.1A>G (p.Met1Val)	not provided [RCV001901338]\|not specified [RCV004042595]	uncertain significance	9	98807699	98807699	Human		name
8595360	CV16309	single nucleotide variant	NM_024642.5(GALNT12):c.3G>A (p.Met1Ile)	Colorectal cancer, susceptibility to, 1 [RCV000001332]\|not provided [RCV000475919]\|not specified [RCV004018533]	risk factor\|uncertain significance	9	98807701	98807701	Human	1	name
155664293	CV1786499	single nucleotide variant	NM_024642.5(GALNT12):c.36G>A (p.Arg12=)	not specified [RCV004049704]	likely benign	9	98807734	98807734	Human		name
155734327	CV1802275	single nucleotide variant	NM_024642.5(GALNT12):c.48C>A (p.Arg16=)	not specified [RCV004050181]	likely benign	9	98807746	98807746	Human		name
155704384	CV1810678	single nucleotide variant	NM_024642.5(GALNT12):c.57G>A (p.Glu19=)	not specified [RCV004054112]	likely benign	9	98807755	98807755	Human		name
155705504	CV1811228	single nucleotide variant	NM_024642.5(GALNT12):c.60G>A (p.Ala20=)	not provided [RCV005096898]\|not specified [RCV004052729]	likely benign	9	98807758	98807758	Human		name
155705550	CV1811241	single nucleotide variant	NM_024642.5(GALNT12):c.60G>T (p.Ala20=)	not provided [RCV003108044]\|not specified [RCV004052731]	likely benign	9	98807758	98807758	Human		name
155665635	CV1813877	single nucleotide variant	NM_024642.5(GALNT12):c.79C>T (p.Leu27=)	not specified [RCV004055364]	likely benign	9	98807777	98807777	Human		name
155747193	CV1816743	single nucleotide variant	NM_024642.5(GALNT12):c.78G>A (p.Ala26=)	not specified [RCV004054771]	likely benign	9	98807776	98807776	Human		name
155697912	CV1816805	single nucleotide variant	NM_024642.5(GALNT12):c.81A>G (p.Leu27=)	not specified [RCV004055538]	likely benign	9	98807779	98807779	Human		name
155718748	CV1819431	single nucleotide variant	NM_024642.5(GALNT12):c.73C>T (p.Leu25=)	not specified [RCV004055982]	likely benign	9	98807771	98807771	Human		name
155700375	CV1821065	single nucleotide variant	NM_024642.5(GALNT12):c.8G>A (p.Gly3Glu)	not provided [RCV003546808]\|not specified [RCV004054918]	uncertain significance	9	98807706	98807706	Human		name
155690855	CV1825059	single nucleotide variant	NM_024642.5(GALNT12):c.93C>G (p.Ala31=)	not specified [RCV004055735]	likely benign	9	98807791	98807791	Human		name
155690894	CV1825067	single nucleotide variant	NM_024642.5(GALNT12):c.93C>T (p.Ala31=)	not specified [RCV004056769]	likely benign	9	98807791	98807791	Human		name
155702385	CV1825329	single nucleotide variant	NM_024642.5(GALNT12):c.96G>A (p.Gly32=)	not specified [RCV004057540]	likely benign	9	98807794	98807794	Human		name
155702461	CV1825342	single nucleotide variant	NM_024642.5(GALNT12):c.96G>T (p.Gly32=)	not specified [RCV004057542]	likely benign	9	98807794	98807794	Human		name
155674020	CV1825680	single nucleotide variant	NM_024642.5(GALNT12):c.97C>T (p.Leu33=)	not specified [RCV004057619]	likely benign	9	98807795	98807795	Human		name
155747733	CV1849738	single nucleotide variant	NM_024642.5(GALNT12):c.1A>T (p.Met1Leu)	not specified [RCV004059456]	uncertain significance	9	98807699	98807699	Human		name
156220565	CV2254164	single nucleotide variant	NM_024572.4(GALNT14):c.5G>C (p.Arg2Pro)	not specified [RCV004129594]	uncertain significance	2	31138082	31138082	Human		name
329380145	CV2426416	single nucleotide variant	NM_024642.5(GALNT12):c.40C>T (p.Leu14=)	not specified [RCV004245106]	likely benign	9	98807738	98807738	Human		name
401763919	CV2717164	single nucleotide variant	NM_024642.5(GALNT12):c.7G>C (p.Gly3Arg)	not specified [RCV004324034]	uncertain significance	9	98807705	98807705	Human		name
401777684	CV2729056	single nucleotide variant	NM_024642.5(GALNT12):c.61C>T (p.Leu21=)	not specified [RCV004331725]	likely benign	9	98807759	98807759	Human		name
401942833	CV2835934	single nucleotide variant	NM_024642.5(GALNT12):c.6G>T (p.Trp2Cys)	Colorectal cancer, susceptibility to, 1 [RCV003468244]	uncertain significance	9	98807704	98807704	Human	1	name
405749145	CV3254391	single nucleotide variant	NM_024572.4(GALNT14):c.8G>T (p.Arg3Leu)	not specified [RCV004392470]	uncertain significance	2	31138079	31138079	Human		name
405682808	CV3387736	single nucleotide variant	NM_024642.5(GALNT12):c.87G>T (p.Ala29=)	not specified [RCV004517712]	likely benign	9	98807785	98807785	Human		name
598202986	CV3973879	single nucleotide variant	NM_024572.4(GALNT14):c.5G>A (p.Arg2Gln)	not specified [RCV005337187]	uncertain significance	2	31138082	31138082	Human		name
598202803	CV3977622	single nucleotide variant	NM_024642.5(GALNT12):c.81A>C (p.Leu27=)	not specified [RCV005337159]	likely benign	9	98807779	98807779	Human		name
598190339	CV4008822	single nucleotide variant	NM_024642.5(GALNT12):c.4T>C (p.Trp2Arg)	Colorectal cancer, susceptibility to, 1 [RCV005396321]	uncertain significance	9	98807702	98807702	Human	1	name
14706797	CV638612	single nucleotide variant	NM_024642.5(GALNT12):c.3G>T (p.Met1Ile)	not provided [RCV000792106]\|not specified [RCV004027405]	uncertain significance	9	98807701	98807701	Human		name
15144772	CV692748	single nucleotide variant	NM_024642.5(GALNT12):c.72C>G (p.Leu24=)	not provided [RCV000878274]\|not specified [RCV004027903]	likely benign	9	98807770	98807770	Human		name
25327111	CV809666	single nucleotide variant	NM_024642.5(GALNT12):c.1A>C (p.Met1Leu)	Colorectal cancer, susceptibility to, 1 [RCV005049729]\|not provided [RCV001860753]\|not specified [RCV004030362]	uncertain significance	9	98807699	98807699	Human	1	name
25324412	CV809667	single nucleotide variant	NM_024642.5(GALNT12):c.5G>C (p.Trp2Ser)	Colorectal cancer, susceptibility to, 1 [RCV004570033]\|not provided [RCV001346456]\|not specified [RCV004030858]	uncertain significance	9	98807703	98807703	Human	1	name
25323009	CV809672	single nucleotide variant	NM_024642.5(GALNT12):c.51C>T (p.Gly17=)	not provided [RCV002067667]\|not specified [RCV004030842]	likely benign	9	98807749	98807749	Human		name
25325710	CV809674	single nucleotide variant	NM_024642.5(GALNT12):c.69G>A (p.Val23=)	not specified [RCV004030875]	likely benign	9	98807767	98807767	Human		name
25325713	CV809675	single nucleotide variant	NM_024642.5(GALNT12):c.69G>T (p.Val23=)	not provided [RCV003708558]\|not specified [RCV004030876]	likely benign	9	98807767	98807767	Human		name
25329570	CV809676	single nucleotide variant	NM_024642.5(GALNT12):c.84G>A (p.Leu28=)	not provided [RCV001372662]\|not specified [RCV004030403]	likely benign\|uncertain significance	9	98807782	98807782	Human		name
25329800	CV809677	single nucleotide variant	NM_024642.5(GALNT12):c.87G>A (p.Ala29=)	not provided [RCV003698824]\|not specified [RCV004030410]	likely benign	9	98807785	98807785	Human		name
126920706	CV1046333	single nucleotide variant	NM_024642.5(GALNT12):c.19C>G (p.Arg7Gly)	Colorectal cancer, susceptibility to, 1 [RCV005394983]\|not provided [RCV001363037]\|not specified [RCV004036859]	uncertain significance	9	98807717	98807717	Human	1	name
127305418	CV1140891	single nucleotide variant	NM_024642.5(GALNT12):c.165C>G (p.Thr55=)	not provided [RCV001479769]\|not specified [RCV004037198]	likely benign	9	98807863	98807863	Human		name
127295109	CV1140892	single nucleotide variant	NM_024642.5(GALNT12):c.297G>A (p.Arg99=)	not provided [RCV001497179]\|not specified [RCV004037375]	likely benign	9	98807995	98807995	Human		name
152079387	CV1596876	single nucleotide variant	NM_024642.5(GALNT12):c.231G>T (p.Ala77=)	not provided [RCV002092647]\|not specified [RCV004044973]	likely benign	9	98807929	98807929	Human		name
152087029	CV1601103	single nucleotide variant	NM_024642.5(GALNT12):c.178C>A (p.Arg60=)	not provided [RCV002093623]	likely benign	9	98807876	98807876	Human		name
152142624	CV1639296	single nucleotide variant	NM_024642.5(GALNT12):c.109C>T (p.Leu37=)	not provided [RCV002178259]	likely benign	9	98807807	98807807	Human		name
155667614	CV1789484	single nucleotide variant	NM_024642.5(GALNT12):c.114G>A (p.Arg38=)	not specified [RCV004049612]	likely benign	9	98807812	98807812	Human		name
155744609	CV1789524	single nucleotide variant	NM_024642.5(GALNT12):c.114G>C (p.Arg38=)	not specified [RCV004049623]	likely benign	9	98807812	98807812	Human		name
155738942	CV1801521	single nucleotide variant	NM_024642.5(GALNT12):c.117G>C (p.Ala39=)	not specified [RCV004051509]	likely benign	9	98807815	98807815	Human		name
155728499	CV1812978	single nucleotide variant	NM_024642.5(GALNT12):c.123T>G (p.Arg41=)	not specified [RCV004055843]	likely benign	9	98807821	98807821	Human		name
155699406	CV1824633	single nucleotide variant	NM_024642.5(GALNT12):c.126G>T (p.Gly42=)	not specified [RCV004054872]	likely benign	9	98807824	98807824	Human		name
155732361	CV1826405	single nucleotide variant	NM_024642.5(GALNT12):c.102C>T (p.Gly34=)	not specified [RCV004058815]	likely benign	9	98807800	98807800	Human		name
155689145	CV1826646	single nucleotide variant	NM_024642.5(GALNT12):c.141T>A (p.Ala47=)	not specified [RCV004057235]	likely benign	9	98807839	98807839	Human		name
155691365	CV1827276	single nucleotide variant	NM_024642.5(GALNT12):c.150G>A (p.Pro50=)	not specified [RCV004058588]	likely benign	9	98807848	98807848	Human		name
155712022	CV1827936	single nucleotide variant	NM_024642.5(GALNT12):c.165C>A (p.Thr55=)	not specified [RCV004059766]	likely benign	9	98807863	98807863	Human		name
155701148	CV1828580	single nucleotide variant	NM_024642.5(GALNT12):c.174C>T (p.Pro58=)	not specified [RCV004061282]	likely benign	9	98807872	98807872	Human		name
155680775	CV1829564	single nucleotide variant	NM_024642.5(GALNT12):c.13A>G (p.Thr5Ala)	not specified [RCV004057133]	likely benign	9	98807711	98807711	Human		name
155713494	CV1830044	single nucleotide variant	NM_024642.5(GALNT12):c.147G>A (p.Glu49=)	not specified [RCV004058443]	likely benign	9	98807845	98807845	Human		name
155719995	CV1830665	single nucleotide variant	NM_024642.5(GALNT12):c.156C>G (p.Pro52=)	not specified [RCV004059185]	likely benign	9	98807854	98807854	Human		name
155720045	CV1830672	single nucleotide variant	NM_024642.5(GALNT12):c.156C>T (p.Pro52=)	not specified [RCV004059188]	likely benign	9	98807854	98807854	Human		name
155722064	CV1831284	single nucleotide variant	NM_024642.5(GALNT12):c.171C>A (p.Arg57=)	not specified [RCV004060609]	likely benign	9	98807869	98807869	Human		name
155709766	CV1832713	single nucleotide variant	NM_024642.5(GALNT12):c.138G>C (p.Gly46=)	not specified [RCV004057080]	likely benign	9	98807836	98807836	Human		name
155709780	CV1832716	single nucleotide variant	NM_024642.5(GALNT12):c.138G>T (p.Gly46=)	not specified [RCV004057081]	likely benign	9	98807836	98807836	Human		name
155707191	CV1833376	single nucleotide variant	NM_024642.5(GALNT12):c.153A>G (p.Gly51=)	not specified [RCV004059005]	likely benign	9	98807851	98807851	Human		name
155732644	CV1834065	single nucleotide variant	NM_024642.5(GALNT12):c.162C>T (p.Arg54=)	not specified [RCV004058067]	likely benign	9	98807860	98807860	Human		name
155700417	CV1836737	single nucleotide variant	NM_024642.5(GALNT12):c.144C>T (p.Ala48=)	not specified [RCV004057900]	likely benign	9	98807842	98807842	Human		name
155707157	CV1837321	single nucleotide variant	NM_024642.5(GALNT12):c.153A>C (p.Gly51=)	not specified [RCV004059002]	likely benign	9	98807851	98807851	Human		name
155719245	CV1837339	single nucleotide variant	NM_024642.5(GALNT12):c.159G>T (p.Pro53=)	not specified [RCV004057404]	likely benign	9	98807857	98807857	Human		name
155745157	CV1838047	single nucleotide variant	NM_024642.5(GALNT12):c.168G>T (p.Pro56=)	not specified [RCV004059930]	likely benign	9	98807866	98807866	Human		name
155731297	CV1838616	single nucleotide variant	NM_024642.5(GALNT12):c.177G>C (p.Gly59=)	not specified [RCV004061437]	likely benign	9	98807875	98807875	Human		name
155705962	CV1841201	single nucleotide variant	NM_024642.5(GALNT12):c.108G>C (p.Val36=)	not specified [RCV004062548]	likely benign	9	98807806	98807806	Human		name
155685899	CV1841311	single nucleotide variant	NM_024642.5(GALNT12):c.237C>A (p.Gly79=)	not specified [RCV004063349]	likely benign	9	98807935	98807935	Human		name
155726417	CV1841618	single nucleotide variant	NM_024642.5(GALNT12):c.23G>C (p.Arg8Pro)	Colorectal cancer, susceptibility to, 1 [RCV003465756]\|not provided [RCV003098855]\|not specified [RCV004063407]	uncertain significance	9	98807721	98807721	Human	1	name
155692586	CV1841620	single nucleotide variant	NM_024642.5(GALNT12):c.23G>T (p.Arg8Leu)	not specified [RCV004063408]	uncertain significance	9	98807721	98807721	Human		name
155714000	CV1841769	single nucleotide variant	NM_024642.5(GALNT12):c.249G>A (p.Arg83=)	not specified [RCV004062011]	likely benign	9	98807947	98807947	Human		name
155676576	CV1843690	single nucleotide variant	NM_024642.5(GALNT12):c.204G>T (p.Pro68=)	not specified [RCV004059640]	likely benign	9	98807902	98807902	Human		name
155692724	CV1845773	single nucleotide variant	NM_024642.5(GALNT12):c.25C>T (p.Arg9Cys)	not provided [RCV003102011]\|not specified [RCV004062889]	uncertain significance	9	98807723	98807723	Human		name
155668377	CV1846591	single nucleotide variant	NM_024642.5(GALNT12):c.201G>T (p.Arg67=)	not specified [RCV004059516]	likely benign	9	98807899	98807899	Human		name
155699394	CV1847529	single nucleotide variant	NM_024642.5(GALNT12):c.222G>C (p.Ala74=)	not specified [RCV004061834]	likely benign	9	98807920	98807920	Human		name
155715254	CV1849377	single nucleotide variant	NM_024642.5(GALNT12):c.271C>T (p.Leu91=)	not specified [RCV004064006]	likely benign	9	98807969	98807969	Human		name
155684004	CV1849500	single nucleotide variant	NM_024642.5(GALNT12):c.198G>A (p.Pro66=)	not specified [RCV004061674]	likely benign	9	98807896	98807896	Human		name
155747704	CV1849713	single nucleotide variant	NM_024642.5(GALNT12):c.19C>T (p.Arg7Trp)	not provided [RCV005097880]\|not specified [RCV004061725]	uncertain significance	9	98807717	98807717	Human		name
155685347	CV1850145	single nucleotide variant	NM_024642.5(GALNT12):c.20G>C (p.Arg7Pro)	not specified [RCV004060320]	uncertain significance	9	98807718	98807718	Human		name
155684818	CV1850745	single nucleotide variant	NM_024642.5(GALNT12):c.228C>T (p.Gly76=)	not specified [RCV004062566]	likely benign	9	98807926	98807926	Human		name
155678899	CV1854079	single nucleotide variant	NM_024642.5(GALNT12):c.273G>A (p.Leu91=)	not specified [RCV004064072]	likely benign	9	98807971	98807971	Human		name
155675761	CV1854319	single nucleotide variant	NM_024642.5(GALNT12):c.111G>C (p.Leu37=)	not specified [RCV004063093]	likely benign	9	98807809	98807809	Human		name
156056254	CV2133791	single nucleotide variant	NM_024642.5(GALNT12):c.213G>A (p.Pro71=)	Colorectal cancer, susceptibility to, 1 [RCV005399058]\|not provided [RCV003000043]\|not specified [RCV004068516]	likely benign	9	98807911	98807911	Human	1	name
156232484	CV2199743	single nucleotide variant	NM_022087.4(GALNT11):c.19C>T (p.Arg7Trp)	not specified [RCV004072470]	uncertain significance	7	152094246	152094246	Human		name
329380148	CV2426417	single nucleotide variant	NM_024642.5(GALNT12):c.228C>G (p.Gly76=)	not specified [RCV004245107]	likely benign	9	98807926	98807926	Human		name
329380158	CV2426421	single nucleotide variant	NM_024642.5(GALNT12):c.261G>A (p.Gln87=)	not specified [RCV004245111]	likely benign	9	98807959	98807959	Human		name
329371625	CV2454817	single nucleotide variant	NM_024572.4(GALNT14):c.14C>G (p.Thr5Ser)	not specified [RCV004270329]	uncertain significance	2	31138073	31138073	Human		name
401763930	CV2717168	single nucleotide variant	NM_024642.5(GALNT12):c.10C>T (p.Arg4Cys)	not specified [RCV004324038]	uncertain significance	9	98807708	98807708	Human		name
401745545	CV2729054	single nucleotide variant	NM_024642.5(GALNT12):c.26G>T (p.Arg9Leu)	not specified [RCV004331723]	uncertain significance	9	98807724	98807724	Human		name
401889273	CV2760587	single nucleotide variant	NM_024642.5(GALNT12):c.234G>A (p.Arg78=)	not specified [RCV004334236]	likely benign	9	98807932	98807932	Human		name
401941300	CV2835937	single nucleotide variant	NM_024642.5(GALNT12):c.14C>T (p.Thr5Met)	Colorectal cancer, susceptibility to, 1 [RCV003461640]	uncertain significance	9	98807712	98807712	Human	1	name
401962189	CV2842991	single nucleotide variant	NM_024642.5(GALNT12):c.247C>A (p.Arg83=)	not provided [RCV003477247]	likely benign	9	98807945	98807945	Human		name
405749039	CV3254375	single nucleotide variant	NM_052917.4(GALNT13):c.23A>G (p.Lys8Arg)	not specified [RCV004392454]	uncertain significance	2	153944520	153944520	Human		name
405682623	CV3387688	single nucleotide variant	NM_024642.5(GALNT12):c.141T>C (p.Ala47=)	not specified [RCV004517667]	likely benign	9	98807839	98807839	Human		name
405682690	CV3387707	single nucleotide variant	NM_024642.5(GALNT12):c.20G>A (p.Arg7Gln)	not specified [RCV004517683]	uncertain significance	9	98807718	98807718	Human		name
405682700	CV3387709	single nucleotide variant	NM_024642.5(GALNT12):c.216G>T (p.Ala72=)	not specified [RCV004517685]	likely benign	9	98807914	98807914	Human		name
407486920	CV3436205	single nucleotide variant	NM_198321.4(GALNT10):c.20G>A (p.Arg7Gln)	not specified [RCV004619178]	uncertain significance	5	154190886	154190886	Human		name
407503278	CV3436241	single nucleotide variant	NM_024642.5(GALNT12):c.168G>C (p.Pro56=)	not specified [RCV004623714]	likely benign	9	98807866	98807866	Human		name
407503362	CV3436264	single nucleotide variant	NM_024642.5(GALNT12):c.222G>T (p.Ala74=)	not specified [RCV004623737]	likely benign	9	98807920	98807920	Human		name
407503379	CV3436269	single nucleotide variant	NM_024642.5(GALNT12):c.267G>A (p.Glu89=)	not specified [RCV004623742]	likely benign	9	98807965	98807965	Human		name
597779791	CV3673609	single nucleotide variant	NM_024642.5(GALNT12):c.294G>A (p.Val98=)	not specified [RCV004930469]	likely benign	9	98807992	98807992	Human		name
597753898	CV3673632	single nucleotide variant	NM_024642.5(GALNT12):c.276G>A (p.Arg92=)	not specified [RCV004924245]	likely benign	9	98807974	98807974	Human		name
12897074	CV397037	single nucleotide variant	NM_024642.5(GALNT12):c.25C>G (p.Arg9Gly)	Colorectal cancer, susceptibility to, 1 [RCV003463949]\|not provided [RCV000457022]\|not specified [RCV004022804]	likely benign\|uncertain significance	9	98807723	98807723	Human	1	name
12898181	CV397586	single nucleotide variant	NM_024642.5(GALNT12):c.138G>A (p.Gly46=)	Colorectal cancer, susceptibility to, 1 [RCV005398663]\|not provided [RCV000473295]\|not specified [RCV004023011]	benign\|likely benign	9	98807836	98807836	Human	1	name
598189631	CV4008726	single nucleotide variant	NM_024642.5(GALNT12):c.135C>T (p.Ala45=)	Colorectal cancer, susceptibility to, 1 [RCV005396225]	likely benign	9	98807833	98807833	Human	1	name
598189948	CV4008768	single nucleotide variant	NM_024642.5(GALNT12):c.174C>G (p.Pro58=)	Colorectal cancer, susceptibility to, 1 [RCV005396267]	likely benign	9	98807872	98807872	Human	1	name
13492912	CV475195	single nucleotide variant	NM_024642.5(GALNT12):c.132G>A (p.Gly44=)	not specified [RCV004024558]	likely benign	9	98807830	98807830	Human		name
14739691	CV638613	single nucleotide variant	NM_024642.5(GALNT12):c.11G>A (p.Arg4His)	Colorectal cancer, susceptibility to, 1 [RCV003461272]\|not provided [RCV000821467]\|not specified [RCV004029069]	uncertain significance	9	98807709	98807709	Human	1	name
15152383	CV687569	single nucleotide variant	NM_024642.5(GALNT12):c.129C>T (p.Ala43=)	Colorectal cancer, susceptibility to, 1 [RCV005392479]\|not provided [RCV000867431]\|not specified [RCV004027700]	likely benign	9	98807827	98807827	Human	1	name
15112110	CV692749	single nucleotide variant	NM_024642.5(GALNT12):c.277C>T (p.Leu93=)	not provided [RCV000872466]\|not specified [RCV004027809]	likely benign	9	98807975	98807975	Human		name
15164075	CV723698	single nucleotide variant	NM_024642.5(GALNT12):c.288G>A (p.Glu96=)	not provided [RCV000882116]\|not specified [RCV004028313]	likely benign	9	98807986	98807986	Human		name
15172561	CV737273	single nucleotide variant	NM_024642.5(GALNT12):c.171C>T (p.Arg57=)	not provided [RCV000905690]\|not specified [RCV004028562]	likely benign	9	98807869	98807869	Human		name
25328111	CV809668	single nucleotide variant	NM_024642.5(GALNT12):c.22C>T (p.Arg8Trp)	Colorectal cancer, susceptibility to, 1 [RCV003467622]\|not provided [RCV001860784]\|not specified [RCV004030369]	uncertain significance	9	98807720	98807720	Human	1	name
25329194	CV809678	single nucleotide variant	NM_024642.5(GALNT12):c.108G>T (p.Val36=)	not provided [RCV001489180]\|not specified [RCV004030393]	likely benign	9	98807806	98807806	Human		name
25325603	CV809686	single nucleotide variant	NM_024642.5(GALNT12):c.165C>T (p.Thr55=)	not provided [RCV001461621]\|not specified [RCV004030342]	likely benign	9	98807863	98807863	Human		name
25326664	CV809690	single nucleotide variant	NM_024642.5(GALNT12):c.189G>T (p.Pro63=)	not provided [RCV002479209]\|not specified [RCV004030356]	likely benign	9	98807887	98807887	Human		name
25328962	CV809699	single nucleotide variant	NM_024642.5(GALNT12):c.285G>A (p.Glu95=)	not specified [RCV004030384]	likely benign	9	98807983	98807983	Human		name
25329324	CV809701	single nucleotide variant	NM_024642.5(GALNT12):c.291C>T (p.Ser97=)	not specified [RCV004030399]	likely benign	9	98807989	98807989	Human		name
126771019	CV1008802	single nucleotide variant	NM_024642.5(GALNT12):c.66G>T (p.Leu22Phe)	Colorectal cancer, susceptibility to, 1 [RCV003462897]\|not provided [RCV001322911]\|not specified [RCV004035085]	uncertain significance	9	98807764	98807764	Human	1	name
126920909	CV1046339	single nucleotide variant	NM_024642.5(GALNT12):c.354C>A (p.Pro118=)	not provided [RCV001374086]	likely benign\|uncertain significance	9	98808052	98808052	Human		name
127270067	CV1076838	single nucleotide variant	NM_024642.5(GALNT12):c.940C>T (p.Leu314=)	not provided [RCV001404880]	likely benign	9	98835271	98835271	Human		name
127282487	CV1098475	single nucleotide variant	NM_024642.5(GALNT12):c.339G>A (p.Leu113=)	not provided [RCV001447873]\|not specified [RCV004038460]	likely benign	9	98808037	98808037	Human		name
127320336	CV1120065	single nucleotide variant	NM_024642.5(GALNT12):c.357G>A (p.Glu119=)	not provided [RCV001466888]\|not specified [RCV004038661]	likely benign	9	98808055	98808055	Human		name
127328503	CV1120066	single nucleotide variant	NM_024642.5(GALNT12):c.501G>A (p.Leu167=)	not provided [RCV001469573]	likely benign	9	98823385	98823385	Human		name
127304534	CV1140893	single nucleotide variant	NM_024642.5(GALNT12):c.546C>T (p.His182=)	not provided [RCV001499645]\|not specified [RCV002476800]	benign\|likely benign	9	98826756	98826756	Human		name
127309826	CV1140894	single nucleotide variant	NM_024642.5(GALNT12):c.804G>T (p.Leu268=)	not provided [RCV001480998]\|not specified [RCV004037212]	likely benign	9	98831844	98831844	Human		name
151750402	CV1430463	single nucleotide variant	NM_024642.5(GALNT12):c.44G>T (p.Arg15Leu)	not provided [RCV002006807]\|not specified [RCV004046181]	uncertain significance	9	98807742	98807742	Human		name
151749722	CV1487662	single nucleotide variant	NM_024642.5(GALNT12):c.576G>A (p.Ser192=)	not provided [RCV001948017]\|not specified [RCV004043550]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	9	98826786	98826786	Human		name
151719099	CV1505791	single nucleotide variant	NM_024642.5(GALNT12):c.86C>A (p.Ala29Glu)	not provided [RCV002039797]\|not specified [RCV004038942]	uncertain significance	9	98807784	98807784	Human		name
152161337	CV1606144	single nucleotide variant	NM_024642.5(GALNT12):c.603C>T (p.Arg201=)	not provided [RCV002180988]\|not specified [RCV004047076]	likely benign	9	98826813	98826813	Human		name
152121005	CV1613127	single nucleotide variant	NM_024642.5(GALNT12):c.885G>A (p.Arg295=)	not provided [RCV002154254]\|not specified [RCV004047025]	likely benign	9	98831925	98831925	Human		name
152157218	CV1615877	single nucleotide variant	NM_024642.5(GALNT12):c.498C>T (p.Ile166=)	not provided [RCV002158993]	likely benign	9	98823382	98823382	Human		name
152077610	CV1632905	single nucleotide variant	NM_024642.5(GALNT12):c.627G>T (p.Val209=)	not provided [RCV002170129]	likely benign	9	98826837	98826837	Human		name
155716015	CV1785071	single nucleotide variant	NM_024642.5(GALNT12):c.309T>C (p.Ile103=)	not specified [RCV004048327]	likely benign	9	98808007	98808007	Human		name
155732182	CV1785679	single nucleotide variant	NM_024642.5(GALNT12):c.336A>C (p.Ser112=)	not specified [RCV004047851]	likely benign	9	98808034	98808034	Human		name
155729516	CV1786256	single nucleotide variant	NM_024642.5(GALNT12):c.354C>T (p.Pro118=)	not specified [RCV004049098]	likely benign	9	98808052	98808052	Human		name
155694461	CV1787274	single nucleotide variant	NM_024642.5(GALNT12):c.390T>C (p.Tyr130=)	not specified [RCV004050382]	likely benign	9	98823274	98823274	Human		name
155688513	CV1788949	single nucleotide variant	NM_024642.5(GALNT12):c.348C>T (p.Arg116=)	not specified [RCV004048648]	likely benign	9	98808046	98808046	Human		name
155689463	CV1789055	single nucleotide variant	NM_024642.5(GALNT12):c.349C>T (p.Leu117=)	not specified [RCV004048665]	likely benign	9	98808047	98808047	Human		name
155724460	CV1790825	single nucleotide variant	NM_024642.5(GALNT12):c.417T>A (p.Ser139=)	not specified [RCV004051847]	likely benign	9	98823301	98823301	Human		name
155685599	CV1793390	single nucleotide variant	NM_024642.5(GALNT12):c.37G>A (p.Glu13Lys)	not specified [RCV004048112]	uncertain significance	9	98807735	98807735	Human		name
155721559	CV1793591	single nucleotide variant	NM_024642.5(GALNT12):c.381G>A (p.Glu127=)	not specified [RCV004048154]	likely benign	9	98823265	98823265	Human		name
155696287	CV1793654	single nucleotide variant	NM_024642.5(GALNT12):c.396T>C (p.Tyr132=)	not specified [RCV004050506]	likely benign	9	98823280	98823280	Human		name
155692131	CV1794807	single nucleotide variant	NM_024642.5(GALNT12):c.312C>T (p.Asn104=)	not provided [RCV003102311]\|not specified [RCV004048410]	likely benign\|conflicting interpretations of pathogenicity	9	98808010	98808010	Human		name
155676517	CV1796154	single nucleotide variant	NM_024642.5(GALNT12):c.35G>T (p.Arg12Leu)	not specified [RCV004049210]	uncertain significance	9	98807733	98807733	Human		name
155734714	CV1799081	single nucleotide variant	NM_024642.5(GALNT12):c.492G>A (p.Pro164=)	not specified [RCV004050242]	likely benign	9	98823376	98823376	Human		name
155668115	CV1799846	single nucleotide variant	NM_024642.5(GALNT12):c.543G>A (p.Glu181=)	not specified [RCV004053078]	likely benign	9	98826753	98826753	Human		name
155696242	CV1800682	single nucleotide variant	NM_024642.5(GALNT12):c.59C>A (p.Ala20Glu)	not specified [RCV004052546]	uncertain significance	9	98807757	98807757	Human		name
155696677	CV1800785	single nucleotide variant	NM_024642.5(GALNT12):c.600C>A (p.Ile200=)	not specified [RCV004052570]	likely benign	9	98826810	98826810	Human		name
155672840	CV1801161	single nucleotide variant	NM_024642.5(GALNT12):c.62T>G (p.Leu21Arg)	not specified [RCV004053807]	uncertain significance	9	98807760	98807760	Human		name
155735485	CV1801666	single nucleotide variant	NM_024642.5(GALNT12):c.462G>A (p.Arg154=)	not specified [RCV004051538]	likely benign	9	98823346	98823346	Human		name
155734251	CV1802242	single nucleotide variant	NM_024642.5(GALNT12):c.489C>A (p.Ser163=)	not specified [RCV004050173]	likely benign	9	98823373	98823373	Human		name
155722575	CV1802655	single nucleotide variant	NM_024642.5(GALNT12):c.513G>C (p.Val171=)	not specified [RCV004051076]	likely benign	9	98823397	98823397	Human		name
155688232	CV1803817	single nucleotide variant	NM_024642.5(GALNT12):c.594C>T (p.Arg198=)	not specified [RCV004052482]	uncertain significance	9	98826804	98826804	Human		name
155722707	CV1804466	single nucleotide variant	NM_024642.5(GALNT12):c.64T>G (p.Leu22Val)	not specified [RCV004054331]	uncertain significance	9	98807762	98807762	Human		name
155724617	CV1804711	single nucleotide variant	NM_024642.5(GALNT12):c.654G>T (p.Ala218=)	not provided [RCV003098286]\|not specified [RCV004054393]	likely benign	9	98826864	98826864	Human		name
155711513	CV1807872	single nucleotide variant	NM_024642.5(GALNT12):c.642G>T (p.Leu214=)	not provided [RCV003660943]\|not specified [RCV004053978]	likely benign	9	98826852	98826852	Human		name
155713722	CV1808207	single nucleotide variant	NM_024642.5(GALNT12):c.648G>T (p.Ala216=)	not specified [RCV004054316]	likely benign	9	98826858	98826858	Human		name
155729569	CV1808418	single nucleotide variant	NM_024642.5(GALNT12):c.44G>C (p.Arg15Pro)	not specified [RCV004050810]	uncertain significance	9	98807742	98807742	Human		name
155731889	CV1808729	single nucleotide variant	NM_024642.5(GALNT12):c.453T>C (p.Thr151=)	not specified [RCV004051398]	likely benign	9	98823337	98823337	Human		name
155736853	CV1809108	single nucleotide variant	NM_024642.5(GALNT12):c.477C>T (p.Val159=)	not specified [RCV004052114]	likely benign	9	98823361	98823361	Human		name
155725732	CV1811761	single nucleotide variant	NM_024642.5(GALNT12):c.657G>T (p.Ala219=)	not specified [RCV004054428]	likely benign	9	98826867	98826867	Human		name
155667106	CV1812076	single nucleotide variant	NM_024642.5(GALNT12):c.663C>T (p.Gly221=)	not specified [RCV004054493]	likely benign	9	98826873	98826873	Human		name
155680469	CV1812641	single nucleotide variant	NM_024642.5(GALNT12):c.721C>T (p.Leu241=)	not specified [RCV004055774]	likely benign	9	98826931	98826931	Human		name
155681119	CV1812787	single nucleotide variant	NM_024642.5(GALNT12):c.724C>T (p.Leu242=)	not specified [RCV004055810]	likely benign	9	98826934	98826934	Human		name
155698410	CV1813180	single nucleotide variant	NM_024642.5(GALNT12):c.756G>T (p.Val252=)	not specified [RCV004056407]	likely benign	9	98831796	98831796	Human		name
155707639	CV1813481	single nucleotide variant	NM_024642.5(GALNT12):c.762C>T (p.Cys254=)	not provided [RCV003103422]\|not specified [RCV004056477]	likely benign	9	98831802	98831802	Human		name
155747481	CV1813705	single nucleotide variant	NM_024642.5(GALNT12):c.795C>T (p.Phe265=)	not provided [RCV003099803]\|not specified [RCV004054813]	likely benign	9	98831835	98831835	Human		name
155665625	CV1813875	single nucleotide variant	NM_024642.5(GALNT12):c.79C>G (p.Leu27Val)	not specified [RCV004055363]	uncertain significance	9	98807777	98807777	Human		name
155689157	CV1814425	single nucleotide variant	NM_024642.5(GALNT12):c.876G>A (p.Glu292=)	not provided [RCV003560991]\|not specified [RCV004056696]	likely benign	9	98831916	98831916	Human		name
155682190	CV1814819	single nucleotide variant	NM_024642.5(GALNT12):c.921T>C (p.Ser307=)	not specified [RCV004055609]	likely benign	9	98835252	98835252	Human		name
155680273	CV1815911	single nucleotide variant	NM_024642.5(GALNT12):c.720G>A (p.Pro240=)	not specified [RCV004055758]	likely benign	9	98826930	98826930	Human		name
155680293	CV1815916	single nucleotide variant	NM_024642.5(GALNT12):c.720G>T (p.Pro240=)	not specified [RCV004055759]	likely benign	9	98826930	98826930	Human		name
155697516	CV1816320	single nucleotide variant	NM_024642.5(GALNT12):c.753A>C (p.Ala251=)	not specified [RCV004056376]	likely benign	9	98831793	98831793	Human		name
155741675	CV1816464	single nucleotide variant	NM_024642.5(GALNT12):c.783C>T (p.Asp261=)	not specified [RCV004054725]	likely benign	9	98831823	98831823	Human		name
155681732	CV1817298	single nucleotide variant	NM_024642.5(GALNT12):c.864C>T (p.His288=)	not specified [RCV004056589]	likely benign	9	98831904	98831904	Human		name
155722182	CV1817482	single nucleotide variant	NM_024642.5(GALNT12):c.86C>G (p.Ala29Gly)	not provided [RCV003103527]\|not specified [RCV004599330]	uncertain significance	9	98807784	98807784	Human		name
155668540	CV1818199	single nucleotide variant	NM_024642.5(GALNT12):c.960A>G (p.Lys320=)	not specified [RCV004056949]	likely benign	9	98835291	98835291	Human		name
155737711	CV1820106	single nucleotide variant	NM_024642.5(GALNT12):c.77C>A (p.Ala26Glu)	not specified [RCV004054693]	uncertain significance	9	98807775	98807775	Human		name
155744763	CV1820619	single nucleotide variant	NM_024642.5(GALNT12):c.852G>A (p.Val284=)	not provided [RCV003718562]\|not specified [RCV004056228]	likely benign	9	98831892	98831892	Human		name
155714792	CV1820869	single nucleotide variant	NM_024642.5(GALNT12):c.85G>A (p.Ala29Thr)	Colorectal cancer, susceptibility to, 1 [RCV005397405]\|not specified [RCV004056547]	uncertain significance	9	98807783	98807783	Human	1	name
155700527	CV1821092	single nucleotide variant	NM_024642.5(GALNT12):c.900C>A (p.Ser300=)	not specified [RCV004054923]	likely benign	9	98831940	98831940	Human		name
155700563	CV1821099	single nucleotide variant	NM_024642.5(GALNT12):c.900C>T (p.Ser300=)	not specified [RCV004054925]	likely benign	9	98831940	98831940	Human		name
155692013	CV1821517	single nucleotide variant	NM_024642.5(GALNT12):c.94G>A (p.Gly32Arg)	not provided [RCV005097345]\|not specified [RCV004056866]	uncertain significance	9	98807792	98807792	Human		name
155669662	CV1822123	single nucleotide variant	NM_024642.5(GALNT12):c.670C>T (p.Leu224=)	not provided [RCV003476972]\|not specified [RCV004052739]	likely benign\|uncertain significance	9	98826880	98826880	Human		name
155717113	CV1822883	single nucleotide variant	NM_024642.5(GALNT12):c.732G>A (p.Arg244=)	not provided [RCV003103391]\|not specified [RCV004055908]	likely benign\|uncertain significance	9	98831772	98831772	Human		name
155666373	CV1823628	single nucleotide variant	NM_024642.5(GALNT12):c.801C>T (p.Tyr267=)	not specified [RCV004055387]	likely benign	9	98831841	98831841	Human		name
155704851	CV1823973	single nucleotide variant	NM_024642.5(GALNT12):c.83T>C (p.Leu28Pro)	not specified [RCV004056114]	uncertain significance	9	98807781	98807781	Human		name
155712051	CV1824221	single nucleotide variant	NM_024642.5(GALNT12):c.846G>A (p.Arg282=)	not specified [RCV004056169]	likely benign	9	98831886	98831886	Human		name
155699136	CV1824550	single nucleotide variant	NM_024642.5(GALNT12):c.88T>G (p.Leu30Val)	not specified [RCV004054854]	uncertain significance	9	98807786	98807786	Human		name
155699331	CV1824611	single nucleotide variant	NM_024642.5(GALNT12):c.891G>C (p.Arg297=)	not specified [RCV004054867]	likely benign	9	98831931	98831931	Human		name
155684643	CV1824956	single nucleotide variant	NM_024642.5(GALNT12):c.936T>A (p.Gly312=)	not specified [RCV004055716]	likely benign	9	98835267	98835267	Human		name
155673071	CV1825480	single nucleotide variant	NM_024642.5(GALNT12):c.973C>T (p.Leu325=)	not specified [RCV004057569]	likely benign	9	98835304	98835304	Human		name
155673795	CV1825637	single nucleotide variant	NM_024642.5(GALNT12):c.978G>A (p.Gly326=)	not specified [RCV004057609]	likely benign	9	98835309	98835309	Human		name
155675534	CV1828965	single nucleotide variant	NM_024642.5(GALNT12):c.98T>C (p.Leu33Pro)	Colorectal cancer, susceptibility to, 1 [RCV003464504]\|not specified [RCV004057692]	uncertain significance	9	98807796	98807796	Human	1	name
155675591	CV1828975	single nucleotide variant	NM_024642.5(GALNT12):c.990A>G (p.Thr330=)	not specified [RCV004057696]	likely benign	9	98835321	98835321	Human		name
155739499	CV1846005	deletion	NM_024642.5(GALNT12):c.191del (p.Val64fs)	not specified [RCV004060853]	uncertain significance	9	98807889	98807889	Human		name
155667891	CV1856063	single nucleotide variant	NM_024642.5(GALNT12):c.300G>A (p.Leu100=)	not specified [RCV004065504]	likely benign	9	98807998	98807998	Human		name
156217062	CV1869413	single nucleotide variant	NM_024642.5(GALNT12):c.369G>T (p.Pro123=)	not provided [RCV003058770]\|not specified [RCV004070259]	likely benign	9	98808067	98808067	Human		name
156028017	CV2004725	single nucleotide variant	NM_024642.5(GALNT12):c.780C>T (p.Ile260=)	not provided [RCV002658537]\|not specified [RCV004066735]	likely benign	9	98831820	98831820	Human		name
156139686	CV2082250	single nucleotide variant	NM_024642.5(GALNT12):c.924A>G (p.Pro308=)	not provided [RCV002871937]	likely benign	9	98835255	98835255	Human		name
155903270	CV2127095	single nucleotide variant	NM_024642.5(GALNT12):c.52C>G (p.Arg18Gly)	Colorectal cancer, susceptibility to, 1 [RCV003464644]\|not provided [RCV002967551]\|not specified [RCV004068327]	uncertain significance	9	98807750	98807750	Human	1	name
11348101	CV240707	single nucleotide variant	NM_024642.5(GALNT12):c.375C>T (p.Cys125=)	Colorectal cancer, susceptibility to, 1 [RCV005396821]\|not provided [RCV000234383]\|not specified [RCV002479930]	benign\|likely benign	9	98823259	98823259	Human	1	name
11345659	CV240710	single nucleotide variant	NM_024642.5(GALNT12):c.750G>A (p.Ser250=)	Colorectal cancer, susceptibility to, 1 [RCV005396822]\|not provided [RCV000225889]\|not specified [RCV002479931]	benign\|likely benign	9	98831790	98831790	Human	1	name
329358087	CV2422161	single nucleotide variant	NM_024642.5(GALNT12):c.49G>A (p.Gly17Ser)	not specified [RCV004246240]	uncertain significance	9	98807747	98807747	Human		name
329358066	CV2422171	single nucleotide variant	NM_024642.5(GALNT12):c.67G>A (p.Val23Met)	Colorectal cancer, susceptibility to, 1 [RCV004572867]\|not specified [RCV004246250]	uncertain significance	9	98807765	98807765	Human	1	name
329380107	CV2426402	single nucleotide variant	NM_024642.5(GALNT12):c.819G>A (p.Glu273=)	not specified [RCV004245092]	likely benign	9	98831859	98831859	Human		name
329380138	CV2426413	single nucleotide variant	NM_024642.5(GALNT12):c.813C>A (p.Ser271=)	not specified [RCV004245103]	likely benign	9	98831853	98831853	Human		name
329380142	CV2426415	single nucleotide variant	NM_024642.5(GALNT12):c.513G>A (p.Val171=)	not specified [RCV004245105]	likely benign	9	98823397	98823397	Human		name
329380164	CV2426423	single nucleotide variant	NM_024642.5(GALNT12):c.95G>A (p.Gly32Glu)	Colorectal cancer, susceptibility to, 1 [RCV005399277]\|not specified [RCV004245113]	uncertain significance	9	98807793	98807793	Human	1	name
329380167	CV2426424	single nucleotide variant	NM_024642.5(GALNT12):c.645G>A (p.Gly215=)	not specified [RCV004245114]	likely benign	9	98826855	98826855	Human		name
329380171	CV2426426	single nucleotide variant	NM_024642.5(GALNT12):c.774T>C (p.Asp258=)	not specified [RCV004245116]	likely benign	9	98831814	98831814	Human		name
329380177	CV2426428	single nucleotide variant	NM_024642.5(GALNT12):c.609C>T (p.Asn203=)	not specified [RCV004245118]	likely benign	9	98826819	98826819	Human		name
329367063	CV2442075	single nucleotide variant	NM_052917.4(GALNT13):c.28G>A (p.Val10Ile)	not specified [RCV004264277]	uncertain significance	2	153944525	153944525	Human		name
329391831	CV2453177	single nucleotide variant	NM_054110.5(GALNT15):c.38G>C (p.Arg13Thr)	not specified [RCV004279554]	uncertain significance	3	16175189	16175189	Human		name
401749807	CV2711011	single nucleotide variant	NM_022479.3(GALNT17):c.38T>G (p.Leu13Trp)	not specified [RCV004310712]	uncertain significance	7	71132840	71132840	Human		name
401763911	CV2717161	single nucleotide variant	NM_024642.5(GALNT12):c.324C>T (p.Ser108=)	not provided [RCV005102663]\|not specified [RCV004324031]	likely benign	9	98808022	98808022	Human		name
401745497	CV2729030	single nucleotide variant	NM_024642.5(GALNT12):c.35G>A (p.Arg12Gln)	not specified [RCV004331699]	uncertain significance	9	98807733	98807733	Human		name
401777645	CV2729031	single nucleotide variant	NM_024642.5(GALNT12):c.462G>T (p.Arg154=)	not specified [RCV004331700]	uncertain significance	9	98823346	98823346	Human		name
401777656	CV2729040	single nucleotide variant	NM_024642.5(GALNT12):c.939G>T (p.Gly313=)	not specified [RCV004331709]	likely benign	9	98835270	98835270	Human		name
401745531	CV2729048	single nucleotide variant	NM_024642.5(GALNT12):c.570G>A (p.Glu190=)	not specified [RCV004331717]	likely benign	9	98826780	98826780	Human		name
401745540	CV2729053	single nucleotide variant	NM_024642.5(GALNT12):c.83T>G (p.Leu28Arg)	not specified [RCV004331722]	uncertain significance	9	98807781	98807781	Human		name
401871707	CV2760005	single nucleotide variant	NM_024642.5(GALNT12):c.46C>T (p.Arg16Cys)	not specified [RCV004345418]	uncertain significance	9	98807744	98807744	Human		name
401889275	CV2760588	single nucleotide variant	NM_024642.5(GALNT12):c.615A>G (p.Arg205=)	not specified [RCV004334237]	likely benign	9	98826825	98826825	Human		name
401889292	CV2760599	single nucleotide variant	NM_024642.5(GALNT12):c.76G>T (p.Ala26Ser)	not specified [RCV004334248]	uncertain significance	9	98807774	98807774	Human		name
401889294	CV2760602	single nucleotide variant	NM_024642.5(GALNT12):c.802C>T (p.Leu268=)	not specified [RCV004334251]	likely benign	9	98831842	98831842	Human		name
401889301	CV2760607	single nucleotide variant	NM_024642.5(GALNT12):c.945T>C (p.Phe315=)	not specified [RCV004334256]	likely benign	9	98835276	98835276	Human		name
401886356	CV2790260	single nucleotide variant	NM_024642.5(GALNT12):c.53G>C (p.Arg18Pro)	not specified [RCV004364360]	uncertain significance	9	98807751	98807751	Human		name
401941289	CV2835919	deletion	NM_024642.5(GALNT12):c.133del (p.Ala45fs)	Colorectal cancer, susceptibility to, 1 [RCV003461629]	uncertain significance	9	98807828	98807828	Human	1	name
401941373	CV2835927	single nucleotide variant	NM_024642.5(GALNT12):c.52C>T (p.Arg18Trp)	Colorectal cancer, susceptibility to, 1 [RCV003461635]	uncertain significance	9	98807750	98807750	Human	1	name
401962194	CV2842993	single nucleotide variant	NM_024642.5(GALNT12):c.86C>T (p.Ala29Val)	not provided [RCV003477249]	uncertain significance	9	98807784	98807784	Human		name
405208249	CV2909188	single nucleotide variant	NM_024642.5(GALNT12):c.58G>T (p.Ala20Ser)	not provided [RCV003566765]	uncertain significance	9	98807756	98807756	Human		name
405180744	CV2914032	single nucleotide variant	NM_024642.5(GALNT12):c.47G>C (p.Arg16Pro)	not provided [RCV003563941]	uncertain significance	9	98807745	98807745	Human		name
405749104	CV3254385	single nucleotide variant	NM_024572.4(GALNT14):c.399T>C (p.Ser133=)	not specified [RCV004392464]	likely benign	2	30958464	30958464	Human		name
405749257	CV3254407	single nucleotide variant	NM_054110.5(GALNT15):c.540G>A (p.Leu180=)	not specified [RCV004392486]	likely benign	3	16195760	16195760	Human		name
405749561	CV3254449	single nucleotide variant	NM_022479.3(GALNT17):c.91A>G (p.Ile31Val)	not specified [RCV004392529]	uncertain significance	7	71132893	71132893	Human		name
405682708	CV3387711	single nucleotide variant	NM_024642.5(GALNT12):c.29G>A (p.Cys10Tyr)	not specified [RCV004517687]	uncertain significance	9	98807727	98807727	Human		name
405682737	CV3387719	single nucleotide variant	NM_024642.5(GALNT12):c.41T>A (p.Leu14Gln)	not specified [RCV004517695]	uncertain significance	9	98807739	98807739	Human		name
405682761	CV3387725	single nucleotide variant	NM_024642.5(GALNT12):c.660G>A (p.Arg220=)	not specified [RCV004517701]	likely benign	9	98826870	98826870	Human		name
405682769	CV3387727	single nucleotide variant	NM_024642.5(GALNT12):c.684C>T (p.Asp228=)	not specified [RCV004517703]	likely benign	9	98826894	98826894	Human		name
405682774	CV3387728	single nucleotide variant	NM_024642.5(GALNT12):c.74T>C (p.Leu25Pro)	not specified [RCV004517704]	uncertain significance	9	98807772	98807772	Human		name
405682787	CV3387731	single nucleotide variant	NM_024642.5(GALNT12):c.807G>T (p.Gly269=)	not specified [RCV004517707]	likely benign	9	98831847	98831847	Human		name
405682791	CV3387732	single nucleotide variant	NM_024642.5(GALNT12):c.80T>C (p.Leu27Pro)	Colorectal cancer, susceptibility to, 1 [RCV005392818]\|not specified [RCV004517708]	uncertain significance	9	98807778	98807778	Human	1	name
405682829	CV3387741	single nucleotide variant	NM_024642.5(GALNT12):c.92C>T (p.Ala31Val)	not specified [RCV004517717]	uncertain significance	9	98807790	98807790	Human		name
405682832	CV3387742	single nucleotide variant	NM_024642.5(GALNT12):c.942G>A (p.Leu314=)	not specified [RCV004517718]	likely benign	9	98835273	98835273	Human		name
407486914	CV3436204	single nucleotide variant	NM_198321.4(GALNT10):c.71A>G (p.Asn24Ser)	not specified [RCV004619177]	uncertain significance	5	154190937	154190937	Human		name
407503218	CV3436224	single nucleotide variant	NM_024642.5(GALNT12):c.765G>T (p.Pro255=)	not specified [RCV004623697]	likely benign	9	98831805	98831805	Human		name
407503229	CV3436227	single nucleotide variant	NM_024642.5(GALNT12):c.759G>A (p.Val253=)	Colorectal cancer, susceptibility to, 1 [RCV005040729]\|not specified [RCV004623700]	likely benign\|uncertain significance	9	98831799	98831799	Human	1	name
407503253	CV3436234	single nucleotide variant	NM_024642.5(GALNT12):c.714G>A (p.Leu238=)	not specified [RCV004623707]	uncertain significance	9	98826924	98826924	Human		name
407503275	CV3436240	single nucleotide variant	NM_024642.5(GALNT12):c.984T>C (p.Tyr328=)	not specified [RCV004623713]	likely benign	9	98835315	98835315	Human		name
407503294	CV3436245	single nucleotide variant	NM_024642.5(GALNT12):c.640C>T (p.Leu214=)	not specified [RCV004623718]	likely benign	9	98826850	98826850	Human		name
407503322	CV3436253	single nucleotide variant	NM_024642.5(GALNT12):c.345C>T (p.Arg115=)	not specified [RCV004623726]	likely benign	9	98808043	98808043	Human		name
407503327	CV3436254	single nucleotide variant	NM_024642.5(GALNT12):c.807G>A (p.Gly269=)	not specified [RCV004623727]	likely benign	9	98831847	98831847	Human		name
597753694	CV3673549	single nucleotide variant	NM_198321.4(GALNT10):c.89T>C (p.Leu30Pro)	not specified [RCV004924196]	uncertain significance	5	154190955	154190955	Human		name
597753752	CV3673567	single nucleotide variant	NM_024642.5(GALNT12):c.315C>T (p.Ile105=)	not specified [RCV004924210]	likely benign	9	98808013	98808013	Human		name
597753781	CV3673580	single nucleotide variant	NM_024642.5(GALNT12):c.89T>C (p.Leu30Ser)	not specified [RCV004924217]	uncertain significance	9	98807787	98807787	Human		name
597753806	CV3673588	single nucleotide variant	NM_024642.5(GALNT12):c.34C>T (p.Arg12Trp)	not specified [RCV004924223]	uncertain significance	9	98807732	98807732	Human		name
597753814	CV3673593	single nucleotide variant	NM_024642.5(GALNT12):c.366C>T (p.Asn122=)	not specified [RCV004924225]	likely benign	9	98808064	98808064	Human		name
597779787	CV3673608	single nucleotide variant	NM_024642.5(GALNT12):c.726G>A (p.Leu242=)	not specified [RCV004930468]	likely benign	9	98826936	98826936	Human		name
597779806	CV3673613	single nucleotide variant	NM_024642.5(GALNT12):c.588G>A (p.Lys196=)	not specified [RCV004930472]	likely benign	9	98826798	98826798	Human		name
597779814	CV3673615	single nucleotide variant	NM_024642.5(GALNT12):c.28T>C (p.Cys10Arg)	not specified [RCV004930474]	uncertain significance	9	98807726	98807726	Human		name
597779852	CV3673633	single nucleotide variant	NM_024642.5(GALNT12):c.672G>A (p.Leu224=)	not specified [RCV004930483]	likely benign	9	98826882	98826882	Human		name
597964141	CV3837858	single nucleotide variant	NM_024642.5(GALNT12):c.95G>T (p.Gly32Val)	not provided [RCV005193842]	uncertain significance	9	98807793	98807793	Human		name
598219432	CV3895658	deletion	NM_024642.5(GALNT12):c.167del (p.Pro56fs)	Colorectal cancer, susceptibility to, 1 [RCV005360498]	uncertain significance	9	98807862	98807862	Human	1	name
12897222	CV397043	single nucleotide variant	NM_024642.5(GALNT12):c.675C>T (p.Thr225=)	not provided [RCV000459131]\|not specified [RCV004023014]	likely benign	9	98826885	98826885	Human		name
598202884	CV3973864	single nucleotide variant	NM_024642.5(GALNT12):c.852G>T (p.Val284=)	not specified [RCV005337172]	likely benign	9	98831892	98831892	Human		name
598202896	CV3973866	single nucleotide variant	NM_024642.5(GALNT12):c.585C>A (p.Pro195=)	not specified [RCV005337174]	likely benign	9	98826795	98826795	Human		name
12897978	CV397475	single nucleotide variant	NM_024642.5(GALNT12):c.903C>G (p.Pro301=)	Colorectal cancer, susceptibility to, 1 [RCV005398670]\|not provided [RCV000470269]\|not specified [RCV004023019]	likely benign	9	98831943	98831943	Human	1	name
12897270	CV397479	single nucleotide variant	NM_024642.5(GALNT12):c.975G>A (p.Leu325=)	Colorectal cancer, susceptibility to, 1 [RCV005398667]\|not provided [RCV000459863]\|not specified [RCV004023017]	benign\|likely benign\|uncertain significance	9	98835306	98835306	Human	1	name
12897856	CV397603	single nucleotide variant	NM_024642.5(GALNT12):c.813C>T (p.Ser271=)	Colorectal cancer, susceptibility to, 1 [RCV005398665]\|not provided [RCV000468423]\|not specified [RCV004023015]	likely benign	9	98831853	98831853	Human	1	name
598202720	CV3977607	single nucleotide variant	NM_024642.5(GALNT12):c.59C>T (p.Ala20Val)	not specified [RCV005337146]	uncertain significance	9	98807757	98807757	Human		name
598202824	CV3977625	single nucleotide variant	NM_024642.5(GALNT12):c.474T>C (p.Ser158=)	not specified [RCV005337162]	likely benign	9	98823358	98823358	Human		name
598202854	CV3977631	single nucleotide variant	NM_024642.5(GALNT12):c.531C>T (p.Tyr177=)	not specified [RCV005337167]	likely benign	9	98823415	98823415	Human		name
598190316	CV4008819	single nucleotide variant	NM_024642.5(GALNT12):c.43C>T (p.Arg15Trp)	Colorectal cancer, susceptibility to, 1 [RCV005396318]	uncertain significance	9	98807741	98807741	Human	1	name
598190576	CV4008854	single nucleotide variant	NM_024642.5(GALNT12):c.71T>C (p.Leu24Pro)	Colorectal cancer, susceptibility to, 1 [RCV005396353]	uncertain significance	9	98807769	98807769	Human	1	name
13493457	CV475015	single nucleotide variant	NM_024642.5(GALNT12):c.849G>T (p.Leu283=)	not provided [RCV003727761]\|not specified [RCV004024529]	likely benign	9	98831889	98831889	Human		name
13466732	CV475037	single nucleotide variant	NM_024642.5(GALNT12):c.477C>G (p.Val159=)	not provided [RCV003736824]\|not specified [RCV004024537]	likely benign	9	98823361	98823361	Human		name
13503045	CV475039	single nucleotide variant	NM_024642.5(GALNT12):c.828C>A (p.Ile276=)	not provided [RCV000872203]\|not specified [RCV004024553]	likely benign	9	98831868	98831868	Human		name
13496346	CV475040	single nucleotide variant	NM_024642.5(GALNT12):c.831C>T (p.Gly277=)	Colorectal cancer, susceptibility to, 1 [RCV005398915]\|not provided [RCV000868693]\|not specified [RCV004024548]	benign\|likely benign	9	98831871	98831871	Human	1	name
13481706	CV475047	single nucleotide variant	NM_024642.5(GALNT12):c.903C>T (p.Pro301=)	not provided [RCV000869088]\|not specified [RCV004024544]	benign\|likely benign	9	98831943	98831943	Human		name
13490339	CV475049	single nucleotide variant	NM_024642.5(GALNT12):c.906C>T (p.Val302=)	not provided [RCV001470502]\|not specified [RCV004024550]	likely benign	9	98831946	98831946	Human		name
13495622	CV475186	single nucleotide variant	NM_024642.5(GALNT12):c.765G>A (p.Pro255=)	Colorectal cancer, susceptibility to, 1 [RCV005398912]\|not provided [RCV000866972]\|not specified [RCV004024525]	likely benign	9	98831805	98831805	Human	1	name
13498689	CV475210	single nucleotide variant	NM_024642.5(GALNT12):c.318C>T (p.Tyr106=)	not specified [RCV004024564]	likely benign	9	98808016	98808016	Human		name
13488326	CV475227	single nucleotide variant	NM_024642.5(GALNT12):c.822C>T (p.Pro274=)	not provided [RCV001484601]\|not specified [RCV004024523]	likely benign	9	98831862	98831862	Human		name
14710344	CV638615	single nucleotide variant	NM_024642.5(GALNT12):c.94G>T (p.Gly32Trp)	Colorectal cancer, susceptibility to, 1 [RCV004569513]\|not provided [RCV000793094]\|not specified [RCV004027432]	uncertain significance	9	98807792	98807792	Human	1	name
15135134	CV687571	single nucleotide variant	NM_024642.5(GALNT12):c.501G>T (p.Leu167=)	not provided [RCV000864256]\|not specified [RCV004027620]	likely benign	9	98823385	98823385	Human		name
15143337	CV687572	single nucleotide variant	NM_024642.5(GALNT12):c.648G>A (p.Ala216=)	not provided [RCV000865715]\|not specified [RCV004027655]	likely benign	9	98826858	98826858	Human		name
15154058	CV687573	single nucleotide variant	NM_024642.5(GALNT12):c.654G>A (p.Ala218=)	not provided [RCV000867776]\|not specified [RCV004027705]	likely benign	9	98826864	98826864	Human		name
15098440	CV697550	single nucleotide variant	NM_024572.4(GALNT14):c.594C>T (p.Leu198=)	not provided [RCV000958559]	benign	2	30955678	30955678	Human		name
15181445	CV701125	single nucleotide variant	NM_024642.5(GALNT12):c.354C>G (p.Pro118=)	not provided [RCV000951978]\|not specified [RCV004029831]	likely benign	9	98808052	98808052	Human		name
15179810	CV701126	single nucleotide variant	NM_024642.5(GALNT12):c.411G>A (p.Arg137=)	not provided [RCV000951604]\|not specified [RCV004029826]	likely benign	9	98823295	98823295	Human		name
15156740	CV737274	single nucleotide variant	NM_024642.5(GALNT12):c.657G>A (p.Ala219=)	not provided [RCV000902385]\|not specified [RCV004028527]	likely benign	9	98826867	98826867	Human		name
15148523	CV737275	single nucleotide variant	NM_024642.5(GALNT12):c.741A>G (p.Glu247=)	not provided [RCV000900735]\|not specified [RCV004028507]	likely benign	9	98831781	98831781	Human		name
15111403	CV751879	single nucleotide variant	NM_024642.5(GALNT12):c.756G>C (p.Val252=)	not provided [RCV000916724]\|not specified [RCV004029402]	likely benign	9	98831796	98831796	Human		name
15123864	CV767575	single nucleotide variant	NM_024642.5(GALNT12):c.336A>G (p.Ser112=)	not provided [RCV000940928]\|not specified [RCV004029709]	likely benign	9	98808034	98808034	Human		name
15193118	CV767576	single nucleotide variant	NM_024642.5(GALNT12):c.516C>T (p.Ile172=)	not provided [RCV000933276]\|not specified [RCV004029601]	likely benign	9	98823400	98823400	Human		name
15189761	CV767577	single nucleotide variant	NM_024642.5(GALNT12):c.672G>T (p.Leu224=)	not provided [RCV000932331]	likely benign	9	98826882	98826882	Human		name
15124077	CV783512	single nucleotide variant	NM_024642.5(GALNT12):c.321C>G (p.Leu107=)	not provided [RCV000979945]	likely benign	9	98808019	98808019	Human		name
25315716	CV809669	single nucleotide variant	NM_024642.5(GALNT12):c.32C>T (p.Pro11Leu)	Colorectal cancer, susceptibility to, 1 [RCV003467654]\|not provided [RCV001322937]\|not specified [RCV004030795]	likely benign\|uncertain significance	9	98807730	98807730	Human	1	name
25318419	CV809670	single nucleotide variant	NM_024642.5(GALNT12):c.40C>G (p.Leu14Val)	not specified [RCV004030812]	uncertain significance	9	98807738	98807738	Human		name
25323491	CV809673	single nucleotide variant	NM_024642.5(GALNT12):c.53G>A (p.Arg18Gln)	not specified [RCV004030847]	uncertain significance	9	98807751	98807751	Human		name
25317176	CV809705	single nucleotide variant	NM_024642.5(GALNT12):c.369G>A (p.Pro123=)	not provided [RCV002069003]\|not specified [RCV004030804]	likely benign	9	98808067	98808067	Human		name
25318139	CV809707	single nucleotide variant	NM_024642.5(GALNT12):c.399T>C (p.Asp133=)	not provided [RCV002067642]\|not specified [RCV004030807]	likely benign	9	98823283	98823283	Human		name
25318496	CV809709	single nucleotide variant	NM_024642.5(GALNT12):c.414A>G (p.Thr138=)	not specified [RCV004030815]	likely benign	9	98823298	98823298	Human		name
25322566	CV809716	single nucleotide variant	NM_024642.5(GALNT12):c.504A>G (p.Leu168=)	not provided [RCV002552371]\|not specified [RCV004030836]	benign\|likely benign	9	98823388	98823388	Human		name
25324094	CV809721	single nucleotide variant	NM_024642.5(GALNT12):c.576G>C (p.Ser192=)	not provided [RCV003736958]\|not specified [RCV004030852]	likely benign	9	98826786	98826786	Human		name
25324355	CV809724	single nucleotide variant	NM_024642.5(GALNT12):c.597G>C (p.Leu199=)	not specified [RCV004030857]	likely benign	9	98826807	98826807	Human		name
25324685	CV809729	single nucleotide variant	NM_024642.5(GALNT12):c.621C>T (p.Gly207=)	not provided [RCV002551911]\|not specified [RCV004030864]	likely benign	9	98826831	98826831	Human		name
25325760	CV809734	single nucleotide variant	NM_024642.5(GALNT12):c.702C>T (p.His234=)	Colorectal cancer, susceptibility to, 1 [RCV005394648]\|not provided [RCV002551944]\|not specified [RCV004030878]	likely benign	9	98826912	98826912	Human	1	name
25327070	CV809740	single nucleotide variant	NM_024642.5(GALNT12):c.807G>C (p.Gly269=)	not specified [RCV004030891]	likely benign	9	98831847	98831847	Human		name
25327327	CV809743	single nucleotide variant	NM_024642.5(GALNT12):c.828C>T (p.Ile276=)	Colorectal cancer, susceptibility to, 1 [RCV005394652]\|not provided [RCV001394358]\|not specified [RCV004030895]	likely benign	9	98831868	98831868	Human	1	name
25329411	CV809745	single nucleotide variant	NM_024642.5(GALNT12):c.837C>T (p.Phe279=)	not provided [RCV001419727]\|not specified [RCV004030400]	benign\|likely benign	9	98831877	98831877	Human		name
25315690	CV809758	single nucleotide variant	NM_024642.5(GALNT12):c.978G>T (p.Gly326=)	not specified [RCV004030794]	likely benign	9	98835309	98835309	Human		name
8625967	CV81111	single nucleotide variant	NM_198321.3(GALNT10):c.312G>A (p.Val104=)	Malignant melanoma [RCV000061189]	not provided	5	154297990	154297990	Human		name
8625968	CV81112	single nucleotide variant	NM_198321.3(GALNT10):c.549C>T (p.Val183=)	Malignant melanoma [RCV000061190]	not provided	5	154329719	154329719	Human		name
26920393	CV836488	single nucleotide variant	NM_024642.5(GALNT12):c.65T>C (p.Leu22Ser)	not provided [RCV001047510]	uncertain significance	9	98807763	98807763	Human		name
8629892	CV85039	single nucleotide variant	NM_052917.3(GALNT13):c.447G>A (p.Glu149=)	Malignant melanoma [RCV000065121]	not provided	2	154242165	154242165	Human		name
8629893	CV85040	single nucleotide variant	NM_052917.3(GALNT13):c.687G>A (p.Arg229=)	Malignant melanoma [RCV000065122]	not provided	2	154245812	154245812	Human		name
8630316	CV85471	single nucleotide variant	NM_024572.3(GALNT14):c.456C>T (p.Phe152=)	Malignant melanoma [RCV000065554]	not provided	2	30958407	30958407	Human		name
8631499	CV86703	single nucleotide variant	NM_198321.3(GALNT10):c.495C>T (p.Val165=)	Malignant melanoma [RCV000066794]	not provided	5	154329665	154329665	Human		name
126766737	CV993620	single nucleotide variant	NM_024642.5(GALNT12):c.56A>C (p.Glu19Ala)	not provided [RCV001302012]	uncertain significance	9	98807754	98807754	Human		name
126750585	CV1008804	single nucleotide variant	NM_024642.5(GALNT12):c.283G>A (p.Glu95Lys)	not provided [RCV001326752]\|not specified [RCV004035216]	uncertain significance	9	98807981	98807981	Human		name
126747494	CV1029363	single nucleotide variant	NM_024642.5(GALNT12):c.158C>T (p.Pro53Leu)	not provided [RCV001337478]\|not specified [RCV004599257]	likely benign\|uncertain significance	9	98807856	98807856	Human		name
126750673	CV1029364	single nucleotide variant	NM_024642.5(GALNT12):c.281A>G (p.Gln94Arg)	Colorectal cancer, susceptibility to, 1 [RCV004570859]\|not provided [RCV001352289]\|not specified [RCV004036680]	uncertain significance	9	98807979	98807979	Human	1	name
126734662	CV1029369	deletion	NM_024642.5(GALNT12):c.874del (p.Glu292fs)	not provided [RCV001349974]	uncertain significance	9	98831914	98831914	Human		name
126923666	CV1046334	single nucleotide variant	NM_024642.5(GALNT12):c.178C>T (p.Arg60Trp)	not provided [RCV001366107]	uncertain significance	9	98807876	98807876	Human		name
126923452	CV1046335	single nucleotide variant	NM_024642.5(GALNT12):c.224T>G (p.Leu75Arg)	not provided [RCV001365863]\|not specified [RCV004036953]	uncertain significance	9	98807922	98807922	Human		name
126924047	CV1046336	single nucleotide variant	NM_024642.5(GALNT12):c.269A>C (p.Glu90Ala)	not provided [RCV001366570]	uncertain significance	9	98807967	98807967	Human		name
127235116	CV1076839	single nucleotide variant	NM_024642.5(GALNT12):c.1464C>T (p.Phe488=)	not provided [RCV001396577]\|not specified [RCV004037770]	likely benign	9	98845982	98845982	Human		name
127248014	CV1076840	single nucleotide variant	NM_024642.5(GALNT12):c.1473G>A (p.Thr491=)	not provided [RCV001399257]\|not specified [RCV004037801]	likely benign	9	98845991	98845991	Human		name
127262446	CV1098476	single nucleotide variant	NM_024642.5(GALNT12):c.1119C>T (p.Arg373=)	not provided [RCV001428322]\|not specified [RCV004038256]	likely benign\|uncertain significance	9	98837055	98837055	Human		name
127252984	CV1098477	single nucleotide variant	NM_024642.5(GALNT12):c.1533A>G (p.Ala511=)	not provided [RCV001436928]\|not specified [RCV004038351]	likely benign	9	98846051	98846051	Human		name
127279387	CV1098479	single nucleotide variant	NM_024642.5(GALNT12):c.1623C>T (p.His541=)	not provided [RCV001445732]\|not specified [RCV004038437]	likely benign	9	98848969	98848969	Human		name
127333245	CV1120070	single nucleotide variant	NM_024642.5(GALNT12):c.1707G>T (p.Ser569=)	not provided [RCV001472754]\|not specified [RCV004037132]	likely benign	9	98849053	98849053	Human		name
127328842	CV1140895	single nucleotide variant	NM_024642.5(GALNT12):c.1308G>C (p.Leu436=)	not provided [RCV001487006]\|not specified [RCV004037272]	likely benign	9	98840097	98840097	Human		name
127322643	CV1140896	single nucleotide variant	NM_024642.5(GALNT12):c.1443G>C (p.Gly481=)	not provided [RCV001505184]\|not specified [RCV004037847]	likely benign	9	98844194	98844194	Human		name
150543917	CV1309873	single nucleotide variant	NM_024642.5(GALNT12):c.208G>T (p.Val70Leu)	not provided [RCV003237615]\|not specified [RCV004040753]	uncertain significance	9	98807906	98807906	Human		name
150543918	CV1309874	single nucleotide variant	NM_024642.5(GALNT12):c.190G>A (p.Val64Ile)	not provided [RCV003237616]\|not specified [RCV004040754]	uncertain significance	9	98807888	98807888	Human		name
151880056	CV1359970	single nucleotide variant	NM_024642.5(GALNT12):c.163A>T (p.Thr55Ser)	not provided [RCV002036742]	uncertain significance	9	98807861	98807861	Human		name
151836358	CV1375092	single nucleotide variant	NM_024642.5(GALNT12):c.226G>C (p.Gly76Arg)	not provided [RCV001921021]\|not specified [RCV004043490]	uncertain significance	9	98807924	98807924	Human		name
151875186	CV1388282	single nucleotide variant	NM_024642.5(GALNT12):c.266A>G (p.Glu89Gly)	Colorectal cancer, susceptibility to, 1 [RCV004571680]\|not provided [RCV001981809]\|not specified [RCV004043679]	uncertain significance	9	98807964	98807964	Human	1	name
151871336	CV1413723	single nucleotide variant	NM_024642.5(GALNT12):c.1320G>A (p.Glu440=)	not provided [RCV001998380]	likely benign\|uncertain significance	9	98840109	98840109	Human		name
151864534	CV1416529	single nucleotide variant	NM_024642.5(GALNT12):c.148C>A (p.Pro50Thr)	not provided [RCV001997566]\|not specified [RCV004599274]	likely benign\|uncertain significance	9	98807846	98807846	Human		name
151835876	CV1436385	single nucleotide variant	NM_024642.5(GALNT12):c.107T>G (p.Val36Gly)	not provided [RCV002014781]\|not specified [RCV004043959]	uncertain significance	9	98807805	98807805	Human		name
151800818	CV1474953	single nucleotide variant	NM_024642.5(GALNT12):c.112C>T (p.Arg38Trp)	Colorectal cancer, susceptibility to, 1 [RCV004571674]\|not provided [RCV001952906]\|not specified [RCV004043171]	uncertain significance	9	98807810	98807810	Human	1	name
151816386	CV1482502	single nucleotide variant	NM_024642.5(GALNT12):c.130G>C (p.Gly44Arg)	not provided [RCV002049354]	uncertain significance	9	98807828	98807828	Human		name
151784484	CV1499070	single nucleotide variant	NM_024642.5(GALNT12):c.236G>A (p.Gly79Asp)	not provided [RCV002026577]	uncertain significance	9	98807934	98807934	Human		name
152051414	CV1538637	single nucleotide variant	NM_024642.5(GALNT12):c.1674T>C (p.Ser558=)	not provided [RCV002189459]	likely benign	9	98849020	98849020	Human		name
152072629	CV1556406	single nucleotide variant	NM_024642.5(GALNT12):c.1077C>T (p.Ser359=)	not provided [RCV002111666]	likely benign	9	98837013	98837013	Human		name
152122717	CV1640987	single nucleotide variant	NM_024642.5(GALNT12):c.1500C>T (p.Thr500=)	not provided [RCV002098381]\|not specified [RCV004045839]	likely benign	9	98846018	98846018	Human		name
152028197	CV1655122	single nucleotide variant	NM_024642.5(GALNT12):c.1716G>A (p.Gln572=)	not provided [RCV002105152]	likely benign	9	98849062	98849062	Human		name
155663933	CV1785859	single nucleotide variant	NM_024642.5(GALNT12):c.113G>A (p.Arg38Gln)	Colorectal cancer, susceptibility to, 1 [RCV004572245]\|not provided [RCV004999693]\|not specified [RCV004047889]	uncertain significance	9	98807811	98807811	Human	1	name
155693413	CV1791569	deletion	NM_024642.5(GALNT12):c.314del (p.Ile105fs)	not specified [RCV004048468]	uncertain significance	9	98808012	98808012	Human		name
155672760	CV1792071	single nucleotide variant	NM_024642.5(GALNT12):c.1011A>G (p.Gly337=)	not specified [RCV004049475]	likely benign	9	98835342	98835342	Human		name
155695724	CV1793962	insertion	NM_024642.5(GALNT12):c.4_5insTG (p.Trp2fs)	not specified [RCV004050584]	uncertain significance	9	98807702	98807703	Human		name
155681824	CV1795641	single nucleotide variant	NM_024642.5(GALNT12):c.1140T>C (p.Ser380=)	not provided [RCV003099468]\|not specified [RCV004047980]	likely benign	9	98837076	98837076	Human		name
155665896	CV1796282	single nucleotide variant	NM_024642.5(GALNT12):c.1152T>A (p.Ala384=)	not specified [RCV004049810]	likely benign	9	98837088	98837088	Human		name
155687387	CV1796916	single nucleotide variant	NM_024642.5(GALNT12):c.115G>A (p.Ala39Thr)	not specified [RCV004050449]	uncertain significance	9	98807813	98807813	Human		name
155673890	CV1801429	deletion	NM_024642.5(GALNT12):c.634del (p.Arg212fs)	not specified [RCV004053872]	uncertain significance	9	98826842	98826842	Human		name
155667086	CV1803139	single nucleotide variant	NM_024642.5(GALNT12):c.1200C>T (p.Pro400=)	not provided [RCV003776104]\|not specified [RCV004053042]	likely benign	9	98837136	98837136	Human		name
155742996	CV1806309	single nucleotide variant	NM_024642.5(GALNT12):c.119A>C (p.Gln40Pro)	not provided [RCV003546782]\|not specified [RCV004052382]	uncertain significance	9	98807817	98807817	Human		name
155743065	CV1806342	single nucleotide variant	NM_024642.5(GALNT12):c.119A>T (p.Gln40Leu)	not specified [RCV004052388]	likely benign\|uncertain significance	9	98807817	98807817	Human		name
155715412	CV1812212	duplication	NM_024642.5(GALNT12):c.689dup (p.His230fs)	not specified [RCV004052935]	uncertain significance	9	98826898	98826899	Human		name
155665070	CV1813760	single nucleotide variant	NM_024642.5(GALNT12):c.1254C>T (p.Asp418=)	not specified [RCV004054822]	likely benign	9	98840043	98840043	Human		name
155729979	CV1814082	deletion	NM_024642.5(GALNT12):c.833del (p.Gly278fs)	not specified [RCV004056053]	uncertain significance	9	98831872	98831872	Human		name
155697450	CV1816311	single nucleotide variant	NM_024642.5(GALNT12):c.1245G>A (p.Gln415=)	not specified [RCV004056374]	likely benign	9	98840034	98840034	Human		name
155724413	CV1817685	single nucleotide variant	NM_024642.5(GALNT12):c.1272C>T (p.Asp424=)	not provided [RCV004999727]\|not specified [RCV004054981]	likely benign\|uncertain significance	9	98840061	98840061	Human		name
155668961	CV1818311	single nucleotide variant	NM_024642.5(GALNT12):c.127G>C (p.Ala43Pro)	not specified [RCV004056979]	uncertain significance	9	98807825	98807825	Human		name
155701243	CV1818319	single nucleotide variant	NM_024642.5(GALNT12):c.127G>T (p.Ala43Ser)	not specified [RCV004056981]	uncertain significance	9	98807825	98807825	Human		name
155675633	CV1818551	single nucleotide variant	NM_024642.5(GALNT12):c.122G>T (p.Arg41Leu)	not specified [RCV004052770]	uncertain significance	9	98807820	98807820	Human		name
155677150	CV1818812	single nucleotide variant	NM_024642.5(GALNT12):c.1230G>T (p.Val410=)	not specified [RCV004052823]	likely benign	9	98840019	98840019	Human		name
155723895	CV1820953	deletion	NM_024642.5(GALNT12):c.897del (p.Gln299fs)	not provided [RCV003103546]\|not specified [RCV004054902]	uncertain significance	9	98831936	98831936	Human		name
155691731	CV1821461	single nucleotide variant	NM_024642.5(GALNT12):c.1278G>A (p.Lys426=)	not specified [RCV004056850]	likely benign	9	98840067	98840067	Human		name
155713082	CV1824370	single nucleotide variant	NM_024642.5(GALNT12):c.1263G>A (p.Gln421=)	not specified [RCV004056200]	likely benign	9	98840052	98840052	Human		name
155730850	CV1825856	deletion	NM_024642.5(GALNT12):c.999del (p.Val334fs)	not specified [RCV004057747]	uncertain significance	9	98835329	98835329	Human		name
155731482	CV1825962	single nucleotide variant	NM_024642.5(GALNT12):c.1285T>C (p.Leu429=)	not provided [RCV003679110]\|not specified [RCV004057771]	likely benign	9	98840074	98840074	Human		name
155677662	CV1826202	single nucleotide variant	NM_024642.5(GALNT12):c.1347C>T (p.Leu449=)	not specified [RCV004058765]	likely benign	9	98844098	98844098	Human		name
155732334	CV1826400	single nucleotide variant	NM_024642.5(GALNT12):c.1356A>G (p.Lys452=)	not specified [RCV004058813]	likely benign	9	98844107	98844107	Human		name
155690366	CV1826820	single nucleotide variant	NM_024642.5(GALNT12):c.1035G>A (p.Arg345=)	not provided [RCV005097511]\|not specified [RCV004057269]	uncertain significance	9	98835366	98835366	Human		name
155690724	CV1826884	single nucleotide variant	NM_024642.5(GALNT12):c.142G>A (p.Ala48Thr)	not specified [RCV004057795]	uncertain significance	9	98807840	98807840	Human		name
155690937	CV1826926	single nucleotide variant	NM_024642.5(GALNT12):c.1431C>T (p.Tyr477=)	not specified [RCV004057807]	likely benign	9	98844182	98844182	Human		name
155691214	CV1826990	single nucleotide variant	NM_024642.5(GALNT12):c.1434C>T (p.Leu478=)	not specified [RCV004057826]	likely benign	9	98844185	98844185	Human		name
155684572	CV1827057	single nucleotide variant	NM_024642.5(GALNT12):c.149C>G (p.Pro50Arg)	not specified [RCV004058534]	uncertain significance	9	98807847	98807847	Human		name
155684580	CV1827059	single nucleotide variant	NM_024642.5(GALNT12):c.149C>T (p.Pro50Leu)	Colorectal cancer, susceptibility to, 1 [RCV003464519]\|not provided [RCV003738246]\|not specified [RCV004599348]	likely benign\|uncertain significance	9	98807847	98807847	Human	1	name
155685196	CV1827252	single nucleotide variant	NM_024642.5(GALNT12):c.1509T>C (p.Pro503=)	not specified [RCV004058580]	likely benign	9	98846027	98846027	Human		name
155712793	CV1828066	single nucleotide variant	NM_024642.5(GALNT12):c.1665G>A (p.Ser555=)	not specified [RCV004059798]	likely benign	9	98849011	98849011	Human		name
155713274	CV1828124	single nucleotide variant	NM_024642.5(GALNT12):c.1668T>C (p.Ser556=)	not specified [RCV004059810]	likely benign	9	98849014	98849014	Human		name
155713496	CV1828151	single nucleotide variant	NM_024642.5(GALNT12):c.166C>G (p.Pro56Ala)	not specified [RCV004059821]	uncertain significance	9	98807864	98807864	Human		name
155700170	CV1828376	single nucleotide variant	NM_024642.5(GALNT12):c.173C>G (p.Pro58Arg)	not specified [RCV004060733]	uncertain significance	9	98807871	98807871	Human		name
155730100	CV1828383	single nucleotide variant	NM_024642.5(GALNT12):c.173C>T (p.Pro58Leu)	not specified [RCV004061218]	likely benign	9	98807871	98807871	Human		name
155684054	CV1830334	single nucleotide variant	NM_024642.5(GALNT12):c.103T>C (p.Ser35Pro)	not specified [RCV004058510]	uncertain significance	9	98807801	98807801	Human		name
155684128	CV1830349	single nucleotide variant	NM_024642.5(GALNT12):c.103T>G (p.Ser35Ala)	not provided [RCV003095237]\|not specified [RCV004599347]	likely benign\|uncertain significance	9	98807801	98807801	Human		name
155709785	CV1830891	single nucleotide variant	NM_024642.5(GALNT12):c.163A>G (p.Thr55Ala)	not specified [RCV004599362]	likely benign\|uncertain significance	9	98807861	98807861	Human		name
155704202	CV1831148	single nucleotide variant	NM_024642.5(GALNT12):c.1650T>A (p.Ala550=)	not specified [RCV004059722]	likely benign	9	98848996	98848996	Human		name
155723373	CV1831524	single nucleotide variant	NM_024642.5(GALNT12):c.1057C>T (p.Leu353=)	not specified [RCV004060678]	likely benign	9	98836993	98836993	Human		name
155723427	CV1831529	single nucleotide variant	NM_024642.5(GALNT12):c.172C>G (p.Pro58Ala)	not specified [RCV004060679]	uncertain significance	9	98807870	98807870	Human		name
155738390	CV1832031	single nucleotide variant	NM_024642.5(GALNT12):c.181C>T (p.Arg61Cys)	not specified [RCV004059371]	uncertain significance	9	98807879	98807879	Human		name
155669487	CV1832167	single nucleotide variant	NM_024642.5(GALNT12):c.1311T>C (p.His437=)	not specified [RCV004058319]	likely benign	9	98840100	98840100	Human		name
155709027	CV1832599	single nucleotide variant	NM_024642.5(GALNT12):c.1386C>T (p.Asn462=)	not specified [RCV004057053]	likely benign	9	98844137	98844137	Human		name
155680727	CV1832939	single nucleotide variant	NM_024642.5(GALNT12):c.139G>T (p.Ala47Ser)	Colorectal cancer, susceptibility to, 1 [RCV005050572]\|not specified [RCV004057131]	uncertain significance	9	98807837	98807837	Human	1	name
155710168	CV1833028	single nucleotide variant	NM_024642.5(GALNT12):c.145G>C (p.Glu49Gln)	not specified [RCV004057954]	uncertain significance	9	98807843	98807843	Human		name
155711005	CV1833138	single nucleotide variant	NM_024642.5(GALNT12):c.1002T>C (p.Val334=)	not specified [RCV004057981]	likely benign	9	98835333	98835333	Human		name
155718474	CV1833807	single nucleotide variant	NM_024642.5(GALNT12):c.155C>A (p.Pro52His)	not specified [RCV004059116]	uncertain significance	9	98807853	98807853	Human		name
155725502	CV1834284	single nucleotide variant	NM_024642.5(GALNT12):c.169C>T (p.Arg57Cys)	not specified [RCV004060500]	uncertain significance	9	98807867	98807867	Human		name
155732723	CV1835437	single nucleotide variant	NM_024642.5(GALNT12):c.188C>T (p.Pro63Leu)	not specified [RCV004060200]	uncertain significance	9	98807886	98807886	Human		name
155719305	CV1835604	single nucleotide variant	NM_024642.5(GALNT12):c.1293T>A (p.Thr431=)	not specified [RCV004058210]	likely benign	9	98840082	98840082	Human		name
155722000	CV1836011	single nucleotide variant	NM_024642.5(GALNT12):c.1308G>A (p.Leu436=)	not specified [RCV004058294]	likely benign	9	98840097	98840097	Human		name
155733614	CV1836158	single nucleotide variant	NM_024642.5(GALNT12):c.136G>T (p.Gly46Trp)	not specified [RCV004058879]	uncertain significance	9	98807834	98807834	Human		name
155699438	CV1836524	single nucleotide variant	NM_024642.5(GALNT12):c.143C>T (p.Ala48Val)	not specified [RCV004057853]	uncertain significance	9	98807841	98807841	Human		name
155700223	CV1836699	single nucleotide variant	NM_024642.5(GALNT12):c.1449C>G (p.Gly483=)	not specified [RCV004057893]	likely benign	9	98844200	98844200	Human		name
155693246	CV1837043	single nucleotide variant	NM_024642.5(GALNT12):c.1524T>C (p.Ala508=)	not specified [RCV004058674]	likely benign	9	98846042	98846042	Human		name
155693453	CV1837088	single nucleotide variant	NM_024642.5(GALNT12):c.1527G>T (p.Val509=)	not specified [RCV004058684]	likely benign	9	98846045	98846045	Human		name
155706341	CV1837134	single nucleotide variant	NM_024642.5(GALNT12):c.152G>A (p.Gly51Glu)	not specified [RCV004058953]	uncertain significance	9	98807850	98807850	Human		name
155723878	CV1837942	single nucleotide variant	NM_024642.5(GALNT12):c.1686C>T (p.Leu562=)	not specified [RCV004059905]	likely benign	9	98849032	98849032	Human		name
155724934	CV1838150	single nucleotide variant	NM_024642.5(GALNT12):c.1695C>T (p.Asp565=)	not specified [RCV004059964]	likely benign	9	98849041	98849041	Human		name
155703258	CV1838422	single nucleotide variant	NM_024642.5(GALNT12):c.176G>T (p.Gly59Val)	not specified [RCV004061389]	uncertain significance	9	98807874	98807874	Human		name
155739001	CV1839193	single nucleotide variant	NM_024642.5(GALNT12):c.182G>A (p.Arg61His)	not provided [RCV003100869]\|not specified [RCV004059415]	uncertain significance	9	98807880	98807880	Human		name
155676500	CV1839566	single nucleotide variant	NM_024642.5(GALNT12):c.1071A>G (p.Pro357=)	not specified [RCV004061552]	likely benign	9	98837007	98837007	Human		name
155677375	CV1839993	single nucleotide variant	NM_024642.5(GALNT12):c.205C>T (p.Pro69Ser)	not specified [RCV004059675]	uncertain significance	9	98807903	98807903	Human		name
155678103	CV1840144	single nucleotide variant	NM_024642.5(GALNT12):c.206C>G (p.Pro69Arg)	not specified [RCV004059698]	uncertain significance	9	98807904	98807904	Human		name
155723891	CV1842148	single nucleotide variant	NM_024642.5(GALNT12):c.1101G>A (p.Lys367=)	not specified [RCV004062089]	likely benign	9	98837037	98837037	Human		name
155744249	CV1843029	single nucleotide variant	NM_024642.5(GALNT12):c.106G>C (p.Val36Leu)	not specified [RCV004060967]	uncertain significance	9	98807804	98807804	Human		name
155674724	CV1843152	single nucleotide variant	NM_024642.5(GALNT12):c.194T>G (p.Met65Arg)	not specified [RCV004061479]	uncertain significance	9	98807892	98807892	Human		name
155670435	CV1843516	single nucleotide variant	NM_024642.5(GALNT12):c.203C>T (p.Pro68Leu)	not specified [RCV004059596]	uncertain significance	9	98807901	98807901	Human		name
155719054	CV1844092	single nucleotide variant	NM_024642.5(GALNT12):c.214G>A (p.Ala72Thr)	not specified [RCV004061030]	uncertain significance	9	98807912	98807912	Human		name
155717228	CV1844884	single nucleotide variant	NM_024642.5(GALNT12):c.235G>A (p.Gly79Ser)	not specified [RCV004063290]	uncertain significance	9	98807933	98807933	Human		name
155671650	CV1845892	single nucleotide variant	NM_024642.5(GALNT12):c.260A>G (p.Gln87Arg)	not specified [RCV004062921]	uncertain significance	9	98807958	98807958	Human		name
155739522	CV1846013	single nucleotide variant	NM_024642.5(GALNT12):c.191T>A (p.Val64Asp)	not specified [RCV004060854]	uncertain significance	9	98807889	98807889	Human		name
155748286	CV1846971	single nucleotide variant	NM_024642.5(GALNT12):c.211C>A (p.Pro71Thr)	not specified [RCV004060394]	uncertain significance	9	98807909	98807909	Human		name
155748293	CV1846977	single nucleotide variant	NM_024642.5(GALNT12):c.211C>T (p.Pro71Ser)	not specified [RCV004060395]	uncertain significance	9	98807909	98807909	Human		name
155685261	CV1847825	single nucleotide variant	NM_024642.5(GALNT12):c.232C>G (p.Arg78Gly)	not specified [RCV004062709]	uncertain significance	9	98807930	98807930	Human		name
155716227	CV1847971	single nucleotide variant	NM_024642.5(GALNT12):c.233G>A (p.Arg78Gln)	not specified [RCV004062736]	uncertain significance	9	98807931	98807931	Human		name
155668541	CV1848729	single nucleotide variant	NM_024642.5(GALNT12):c.256C>G (p.Leu86Val)	not specified [RCV004062774]	uncertain significance	9	98807954	98807954	Human		name
155669103	CV1848876	single nucleotide variant	NM_024642.5(GALNT12):c.257T>C (p.Leu86Pro)	not specified [RCV004062804]	uncertain significance	9	98807955	98807955	Human		name
155672230	CV1849272	single nucleotide variant	NM_024642.5(GALNT12):c.270G>C (p.Glu90Asp)	not specified [RCV004063723]	uncertain significance	9	98807968	98807968	Human		name
155715214	CV1849369	single nucleotide variant	NM_024642.5(GALNT12):c.271C>G (p.Leu91Val)	not provided [RCV003775350]\|not specified [RCV004064005]	uncertain significance	9	98807969	98807969	Human		name
155689956	CV1850615	single nucleotide variant	NM_024642.5(GALNT12):c.1086C>A (p.Gly362=)	not specified [RCV004061730]	likely benign	9	98837022	98837022	Human		name
155706409	CV1850903	single nucleotide variant	NM_024642.5(GALNT12):c.229G>A (p.Ala77Thr)	not specified [RCV004062607]	uncertain significance	9	98807927	98807927	Human		name
155685025	CV1850907	single nucleotide variant	NM_024642.5(GALNT12):c.229G>C (p.Ala77Pro)	not specified [RCV004062608]	uncertain significance	9	98807927	98807927	Human		name
155727319	CV1851507	single nucleotide variant	NM_024642.5(GALNT12):c.242C>T (p.Ala81Val)	not specified [RCV004063780]	uncertain significance	9	98807940	98807940	Human		name
155663822	CV1851973	single nucleotide variant	NM_024642.5(GALNT12):c.254A>G (p.Gln85Arg)	not provided [RCV003101957]\|not specified [RCV004062185]	uncertain significance	9	98807952	98807952	Human		name
155687292	CV1852852	single nucleotide variant	NM_024642.5(GALNT12):c.281A>T (p.Gln94Leu)	not specified [RCV004062313]	uncertain significance	9	98807979	98807979	Human		name
155679638	CV1853041	single nucleotide variant	NM_024642.5(GALNT12):c.1113C>T (p.Tyr371=)	not specified [RCV004064145]	likely benign	9	98837049	98837049	Human		name
155688046	CV1853765	single nucleotide variant	NM_024642.5(GALNT12):c.295C>G (p.Arg99Gly)	not specified [RCV004065358]	uncertain significance	9	98807993	98807993	Human		name
155679212	CV1854184	single nucleotide variant	NM_024642.5(GALNT12):c.274C>G (p.Arg92Gly)	not specified [RCV004064100]	uncertain significance	9	98807972	98807972	Human		name
155679230	CV1854190	single nucleotide variant	NM_024642.5(GALNT12):c.274C>T (p.Arg92Trp)	not specified [RCV004064102]	uncertain significance	9	98807972	98807972	Human		name
155681083	CV1854487	single nucleotide variant	NM_024642.5(GALNT12):c.290G>C (p.Ser97Thr)	not specified [RCV004063134]	likely benign\|uncertain significance	9	98807988	98807988	Human		name
155673319	CV1855616	single nucleotide variant	NM_024642.5(GALNT12):c.286G>A (p.Glu96Lys)	not specified [RCV004062470]	uncertain significance	9	98807984	98807984	Human		name
156206621	CV1922889	duplication	NM_024642.5(GALNT12):c.371dup (p.Cys125fs)	not provided [RCV002643831]	uncertain significance	9	98808068	98808069	Human		name
156001293	CV1987190	single nucleotide variant	NM_024642.5(GALNT12):c.1470C>T (p.Tyr490=)	not provided [RCV002618460]\|not specified [RCV004065849]	likely benign	9	98845988	98845988	Human		name
156293703	CV2047355	single nucleotide variant	NM_024642.5(GALNT12):c.154C>A (p.Pro52Thr)	Colorectal cancer, susceptibility to, 1 [RCV005044984]\|not provided [RCV002770876]	uncertain significance	9	98807852	98807852	Human	1	name
156005689	CV2064800	single nucleotide variant	NM_024642.5(GALNT12):c.120G>C (p.Gln40His)	not provided [RCV002843616]	uncertain significance	9	98807818	98807818	Human		name
156058852	CV2069132	single nucleotide variant	NM_024642.5(GALNT12):c.1686C>G (p.Leu562=)	not provided [RCV002846698]	likely benign	9	98849032	98849032	Human		name
156354510	CV2154124	single nucleotide variant	NM_024642.5(GALNT12):c.164C>A (p.Thr55Asn)	not provided [RCV003031130]	uncertain significance	9	98807862	98807862	Human		name
156366569	CV2203353	single nucleotide variant	NM_024572.4(GALNT14):c.239A>G (p.Asn80Ser)	not specified [RCV004072583]	uncertain significance	2	30992898	30992898	Human		name
156132669	CV2206662	single nucleotide variant	NM_024572.4(GALNT14):c.139G>A (p.Ala47Thr)	not specified [RCV004081000]	uncertain significance	2	30992998	30992998	Human		name
156113153	CV2212666	single nucleotide variant	NM_198321.4(GALNT10):c.134C>G (p.Ala45Gly)	not specified [RCV004085183]	uncertain significance	5	154191000	154191000	Human		name
10767708	CV221936	single nucleotide variant	NM_024642.5(GALNT12):c.1497C>T (p.Asn499=)	Colorectal cancer, susceptibility to, 1 [RCV005396668]\|not provided [RCV000205180]\|not specified [RCV001818505]	benign\|likely benign	9	98846015	98846015	Human	1	name
156080064	CV2226594	single nucleotide variant	NM_022087.4(GALNT11):c.182G>A (p.Arg61Gln)	not specified [RCV004101844]	uncertain significance	7	152094409	152094409	Human		name
156363016	CV2265650	single nucleotide variant	NM_024642.5(GALNT12):c.203C>A (p.Pro68Gln)	not provided [RCV003738316]\|not specified [RCV004124376]	uncertain significance	9	98807901	98807901	Human		name
156361312	CV2269213	single nucleotide variant	NM_198516.3(GALNT18):c.127G>A (p.Gly43Arg)	not specified [RCV004130366]	uncertain significance	11	11621467	11621467	Human		name
156182460	CV2338202	single nucleotide variant	NM_024572.4(GALNT14):c.202C>T (p.Arg68Cys)	not specified [RCV004186271]	uncertain significance	2	30992935	30992935	Human		name
156090951	CV2384600	single nucleotide variant	NM_198516.3(GALNT18):c.136C>A (p.Pro46Thr)	not specified [RCV004232385]	uncertain significance	11	11621458	11621458	Human		name
156088244	CV2388363	single nucleotide variant	NM_022087.4(GALNT11):c.196G>C (p.Val66Leu)	not specified [RCV004234813]	likely benign	7	152094423	152094423	Human		name
156223753	CV2395018	single nucleotide variant	NM_198321.4(GALNT10):c.256C>T (p.Arg86Cys)	not specified [RCV004236709]	uncertain significance	5	154294912	154294912	Human		name
11349454	CV240715	single nucleotide variant	NM_024642.5(GALNT12):c.1551C>T (p.Ile517=)	not provided [RCV000230567]\|not specified [RCV004020876]	likely benign\|uncertain significance	9	98846069	98846069	Human		name
11348153	CV240716	single nucleotide variant	NM_024642.5(GALNT12):c.1677C>T (p.Phe559=)	Colorectal cancer, susceptibility to, 1 [RCV005396819]\|not provided [RCV000234567]\|not specified [RCV002487086]	benign\|likely benign	9	98849023	98849023	Human	1	name
329357749	CV2422157	single nucleotide variant	NM_024642.5(GALNT12):c.1323C>T (p.Asp441=)	not specified [RCV004246237]	likely benign	9	98840112	98840112	Human		name
329383280	CV2422169	single nucleotide variant	NM_024642.5(GALNT12):c.116C>T (p.Ala39Val)	not specified [RCV004246248]	uncertain significance	9	98807814	98807814	Human		name
329372662	CV2424170	single nucleotide variant	NM_054110.5(GALNT15):c.272G>A (p.Arg91Gln)	not specified [RCV004249857]	uncertain significance	3	16175423	16175423	Human		name
329380113	CV2426404	single nucleotide variant	NM_024642.5(GALNT12):c.1293T>C (p.Thr431=)	not specified [RCV004245094]	likely benign	9	98840082	98840082	Human		name
329380116	CV2426405	single nucleotide variant	NM_024642.5(GALNT12):c.215C>G (p.Ala72Gly)	not specified [RCV004245095]	uncertain significance	9	98807913	98807913	Human		name
329380123	CV2426408	single nucleotide variant	NM_024642.5(GALNT12):c.232C>T (p.Arg78Trp)	not specified [RCV004245098]	uncertain significance	9	98807930	98807930	Human		name
329380161	CV2426422	single nucleotide variant	NM_024642.5(GALNT12):c.1182C>G (p.Leu394=)	not specified [RCV004245112]	likely benign	9	98837118	98837118	Human		name
329380174	CV2426427	single nucleotide variant	NM_024642.5(GALNT12):c.1188C>T (p.Tyr396=)	not specified [RCV004245117]	likely benign	9	98837124	98837124	Human		name
329373573	CV2434537	single nucleotide variant	NM_024572.4(GALNT14):c.179G>A (p.Arg60Gln)	not specified [RCV004254239]	uncertain significance	2	30992958	30992958	Human		name
329362669	CV2439024	single nucleotide variant	NM_024642.5(GALNT12):c.295C>T (p.Arg99Trp)	not specified [RCV004264531]	uncertain significance	9	98807993	98807993	Human		name
329362678	CV2439042	single nucleotide variant	NM_024642.5(GALNT12):c.179G>A (p.Arg60Gln)	not specified [RCV004264545]	uncertain significance	9	98807877	98807877	Human		name
329362686	CV2439067	single nucleotide variant	NM_024642.5(GALNT12):c.220G>A (p.Ala74Thr)	not specified [RCV004266360]	uncertain significance	9	98807918	98807918	Human		name
329367073	CV2442081	single nucleotide variant	NM_024642.5(GALNT12):c.145G>A (p.Glu49Lys)	not specified [RCV004264283]	uncertain significance	9	98807843	98807843	Human		name
329362772	CV2449333	single nucleotide variant	NM_024642.5(GALNT12):c.1683A>G (p.Pro561=)	not provided [RCV003565634]\|not specified [RCV004266501]	likely benign	9	98849029	98849029	Human		name
329388341	CV2466276	single nucleotide variant	NM_052917.4(GALNT13):c.155G>A (p.Arg52Lys)	not specified [RCV004280207]	uncertain significance	2	154140349	154140349	Human		name
401763924	CV2717166	single nucleotide variant	NM_024642.5(GALNT12):c.163A>C (p.Thr55Pro)	not specified [RCV004324036]	uncertain significance	9	98807861	98807861	Human		name
401763927	CV2717167	single nucleotide variant	NM_024642.5(GALNT12):c.197C>T (p.Pro66Leu)	not specified [RCV004324037]	uncertain significance	9	98807895	98807895	Human		name
401779555	CV2718616	single nucleotide variant	NM_054110.5(GALNT15):c.173G>A (p.Arg58His)	not specified [RCV004320199]	uncertain significance	3	16175324	16175324	Human		name
401777674	CV2729049	single nucleotide variant	NM_024642.5(GALNT12):c.1434C>G (p.Leu478=)	not specified [RCV004331718]	likely benign	9	98844185	98844185	Human		name
401777677	CV2729050	single nucleotide variant	NM_024642.5(GALNT12):c.1014A>G (p.Glu338=)	not specified [RCV004331719]	likely benign	9	98835345	98835345	Human		name
401857201	CV2760014	single nucleotide variant	NM_024642.5(GALNT12):c.275G>A (p.Arg92Gln)	not specified [RCV004345426]	uncertain significance	9	98807973	98807973	Human		name
401889277	CV2760589	single nucleotide variant	NM_024642.5(GALNT12):c.133G>A (p.Ala45Thr)	Colorectal cancer, susceptibility to, 1 [RCV005399336]\|not specified [RCV004334238]	uncertain significance	9	98807831	98807831	Human	1	name
401862160	CV2760595	single nucleotide variant	NM_024642.5(GALNT12):c.137G>A (p.Gly46Glu)	Colorectal cancer, susceptibility to, 1 [RCV005399337]\|not provided [RCV003777460]\|not specified [RCV004334244]	uncertain significance	9	98807835	98807835	Human	1	name
401862162	CV2760600	single nucleotide variant	NM_024642.5(GALNT12):c.1728C>T (p.Phe576=)	not specified [RCV004334249]	likely benign	9	98849074	98849074	Human		name
401862164	CV2760601	single nucleotide variant	NM_024642.5(GALNT12):c.1083T>G (p.Val361=)	not specified [RCV004334250]	likely benign	9	98837019	98837019	Human		name
401896766	CV2788760	single nucleotide variant	NM_024572.4(GALNT14):c.209G>A (p.Gly70Asp)	not specified [RCV004361228]	uncertain significance	2	30992928	30992928	Human		name
401886354	CV2790261	single nucleotide variant	NM_024642.5(GALNT12):c.1341G>T (p.Gly447=)	not specified [RCV004364361]	uncertain significance	9	98840130	98840130	Human		name
401886352	CV2790262	single nucleotide variant	NM_024642.5(GALNT12):c.292G>T (p.Val98Leu)	not specified [RCV004364362]	uncertain significance	9	98807990	98807990	Human		name
401962186	CV2842989	single nucleotide variant	NM_024642.5(GALNT12):c.1719A>G (p.Lys573=)	not provided [RCV003477245]\|not specified [RCV004364817]	likely benign	9	98849065	98849065	Human		name
405050743	CV2883302	single nucleotide variant	NM_024642.5(GALNT12):c.160C>T (p.Arg54Cys)	not provided [RCV003579769]	uncertain significance	9	98807858	98807858	Human		name
405228231	CV2980672	single nucleotide variant	NM_024642.5(GALNT12):c.1377T>C (p.Phe459=)	not provided [RCV003711073]	likely benign	9	98844128	98844128	Human		name
402493480	CV3008551	single nucleotide variant	NM_024642.5(GALNT12):c.248G>T (p.Arg83Leu)	not provided [RCV003687767]	uncertain significance	9	98807946	98807946	Human		name
405143463	CV3056153	single nucleotide variant	NM_024642.5(GALNT12):c.136G>C (p.Gly46Arg)	not provided [RCV003725852]	uncertain significance	9	98807834	98807834	Human		name
405024637	CV3075914	single nucleotide variant	NM_024642.5(GALNT12):c.265G>A (p.Glu89Lys)	Colorectal cancer, susceptibility to, 1 [RCV004573278]\|not provided [RCV003738688]	uncertain significance	9	98807963	98807963	Human	1	name
405193428	CV3128486	single nucleotide variant	NM_024642.5(GALNT12):c.1008A>T (p.Gly336=)	not provided [RCV003821223]	likely benign	9	98835339	98835339	Human		name
405748868	CV3254351	single nucleotide variant	NM_198321.4(GALNT10):c.163T>A (p.Ser55Thr)	not specified [RCV004392430]	uncertain significance	5	154294819	154294819	Human		name
405749033	CV3254374	single nucleotide variant	NM_052917.4(GALNT13):c.172G>A (p.Gly58Arg)	not specified [RCV004392453]	uncertain significance	2	154140366	154140366	Human		name
405749087	CV3254382	single nucleotide variant	NM_024572.4(GALNT14):c.292C>T (p.His98Tyr)	not specified [RCV004392461]	uncertain significance	2	30992845	30992845	Human		name
405749207	CV3254400	single nucleotide variant	NM_054110.5(GALNT15):c.147C>A (p.Ser49Arg)	not specified [RCV004392479]	uncertain significance	3	16175298	16175298	Human		name
405749449	CV3254434	single nucleotide variant	NM_022479.3(GALNT17):c.182A>G (p.Asp61Gly)	not specified [RCV004392514]	uncertain significance	7	71132984	71132984	Human		name
405749457	CV3254435	single nucleotide variant	NM_022479.3(GALNT17):c.251C>T (p.Ser84Phe)	not specified [RCV004392515]	uncertain significance	7	71335562	71335562	Human		name
405749465	CV3254436	single nucleotide variant	NM_022479.3(GALNT17):c.269G>A (p.Gly90Asp)	not specified [RCV004392516]	uncertain significance	7	71335580	71335580	Human		name
405749472	CV3254437	single nucleotide variant	NM_022479.3(GALNT17):c.281G>A (p.Arg94Gln)	not specified [RCV004392517]	uncertain significance	7	71335592	71335592	Human		name
405683065	CV3387658	single nucleotide variant	NM_024642.5(GALNT12):c.1017C>T (p.Asn339=)	not specified [RCV004517638]	likely benign	9	98835348	98835348	Human		name
405683061	CV3387659	single nucleotide variant	NM_024642.5(GALNT12):c.1023A>G (p.Glu341=)	not specified [RCV004517639]	likely benign	9	98835354	98835354	Human		name
405683045	CV3387664	single nucleotide variant	NM_024642.5(GALNT12):c.104C>G (p.Ser35Trp)	Colorectal cancer, susceptibility to, 1 [RCV005040688]\|not specified [RCV004517643]	likely benign\|uncertain significance	9	98807802	98807802	Human	1	name
405683030	CV3387668	single nucleotide variant	NM_024642.5(GALNT12):c.1110C>T (p.Pro370=)	not specified [RCV004517647]	likely benign	9	98837046	98837046	Human		name
405683022	CV3387670	single nucleotide variant	NM_024642.5(GALNT12):c.1125G>A (p.Lys375=)	not specified [RCV004517649]	likely benign	9	98837061	98837061	Human		name
405683019	CV3387671	single nucleotide variant	NM_024642.5(GALNT12):c.1134C>T (p.Ala378=)	not specified [RCV004517650]	likely benign	9	98837070	98837070	Human		name
405683015	CV3387672	single nucleotide variant	NM_024642.5(GALNT12):c.1143T>C (p.Val381=)	not specified [RCV004517651]	likely benign	9	98837079	98837079	Human		name
405683002	CV3387675	single nucleotide variant	NM_024642.5(GALNT12):c.1206C>T (p.Ala402=)	not specified [RCV004517654]	likely benign	9	98837142	98837142	Human		name
405682854	CV3387676	single nucleotide variant	NM_024642.5(GALNT12):c.1215A>G (p.Glu405=)	not specified [RCV004517655]	likely benign	9	98840004	98840004	Human		name
405682594	CV3387681	single nucleotide variant	NM_024642.5(GALNT12):c.130G>A (p.Gly44Arg)	not specified [RCV004517660]	uncertain significance	9	98807828	98807828	Human		name
405682608	CV3387684	single nucleotide variant	NM_024642.5(GALNT12):c.134C>A (p.Ala45Asp)	not specified [RCV004517663]	uncertain significance	9	98807832	98807832	Human		name
405682612	CV3387685	single nucleotide variant	NM_024642.5(GALNT12):c.134C>T (p.Ala45Val)	not specified [RCV004517664]	uncertain significance	9	98807832	98807832	Human		name
405682630	CV3387690	single nucleotide variant	NM_024642.5(GALNT12):c.146A>C (p.Glu49Ala)	not specified [RCV004517669]	uncertain significance	9	98807844	98807844	Human		name
405682634	CV3387691	single nucleotide variant	NM_024642.5(GALNT12):c.148C>T (p.Pro50Ser)	not specified [RCV004517670]	uncertain significance	9	98807846	98807846	Human		name
405683087	CV3387699	single nucleotide variant	NM_024642.5(GALNT12):c.158C>G (p.Pro53Arg)	not specified [RCV004517676]	likely benign	9	98807856	98807856	Human		name
405682673	CV3387702	single nucleotide variant	NM_024642.5(GALNT12):c.1650T>C (p.Ala550=)	not specified [RCV004517679]	likely benign	9	98848996	98848996	Human		name
405682677	CV3387703	single nucleotide variant	NM_024642.5(GALNT12):c.166C>T (p.Pro56Ser)	not specified [RCV004517680]	uncertain significance	9	98807864	98807864	Human		name
405682685	CV3387706	single nucleotide variant	NM_024642.5(GALNT12):c.206C>A (p.Pro69Gln)	not specified [RCV004517682]	uncertain significance	9	98807904	98807904	Human		name
405682694	CV3387708	single nucleotide variant	NM_024642.5(GALNT12):c.212C>G (p.Pro71Arg)	not specified [RCV004517684]	uncertain significance	9	98807910	98807910	Human		name
405682704	CV3387710	single nucleotide variant	NM_024642.5(GALNT12):c.291C>G (p.Ser97Arg)	not specified [RCV004517686]	uncertain significance	9	98807989	98807989	Human		name
405868878	CV3400642	single nucleotide variant	NM_024642.5(GALNT12):c.230C>T (p.Ala77Val)	Colorectal cancer, susceptibility to, 1 [RCV004576645]	uncertain significance	9	98807928	98807928	Human	1	name
407486887	CV3436200	single nucleotide variant	NM_198321.4(GALNT10):c.143C>A (p.Ala48Glu)	not specified [RCV004619173]	uncertain significance	5	154191009	154191009	Human		name
407503233	CV3436228	single nucleotide variant	NM_024642.5(GALNT12):c.170G>A (p.Arg57His)	not specified [RCV004623701]	uncertain significance	9	98807868	98807868	Human		name
407503236	CV3436229	single nucleotide variant	NM_024642.5(GALNT12):c.122G>A (p.Arg41His)	not specified [RCV004623702]	uncertain significance	9	98807820	98807820	Human		name
407503250	CV3436233	single nucleotide variant	NM_024642.5(GALNT12):c.1230G>A (p.Val410=)	not specified [RCV004623706]	likely benign	9	98840019	98840019	Human		name
407503264	CV3436237	single nucleotide variant	NM_024642.5(GALNT12):c.257T>A (p.Leu86Gln)	not specified [RCV004623710]	uncertain significance	9	98807955	98807955	Human		name
407503271	CV3436239	single nucleotide variant	NM_024642.5(GALNT12):c.125G>C (p.Gly42Ala)	not specified [RCV004623712]	uncertain significance	9	98807823	98807823	Human		name
407503301	CV3436247	single nucleotide variant	NM_024642.5(GALNT12):c.118C>T (p.Gln40Ter)	not specified [RCV004623720]	uncertain significance	9	98807816	98807816	Human		name
407503309	CV3436249	single nucleotide variant	NM_024642.5(GALNT12):c.169C>G (p.Arg57Gly)	not specified [RCV004623722]	uncertain significance	9	98807867	98807867	Human		name
407503316	CV3436251	single nucleotide variant	NM_024642.5(GALNT12):c.1137C>T (p.Asn379=)	not specified [RCV004623724]	likely benign	9	98837073	98837073	Human		name
407503330	CV3436255	single nucleotide variant	NM_024642.5(GALNT12):c.1671C>T (p.Asp557=)	not specified [RCV004623728]	likely benign	9	98849017	98849017	Human		name
407503334	CV3436256	single nucleotide variant	NM_024642.5(GALNT12):c.235G>C (p.Gly79Arg)	not specified [RCV004623729]	uncertain significance	9	98807933	98807933	Human		name
407503354	CV3436262	single nucleotide variant	NM_024642.5(GALNT12):c.215C>T (p.Ala72Val)	not specified [RCV004623735]	uncertain significance	9	98807913	98807913	Human		name
407503359	CV3436263	single nucleotide variant	NM_024642.5(GALNT12):c.1593C>T (p.Phe531=)	not specified [RCV004623736]	likely benign	9	98846111	98846111	Human		name
407503376	CV3436268	single nucleotide variant	NM_024642.5(GALNT12):c.224T>C (p.Leu75Pro)	not specified [RCV004623741]	uncertain significance	9	98807922	98807922	Human		name
407503388	CV3436271	single nucleotide variant	NM_024642.5(GALNT12):c.200G>A (p.Arg67Gln)	not specified [RCV004623744]	uncertain significance	9	98807898	98807898	Human		name
407503427	CV3436282	single nucleotide variant	NM_024572.4(GALNT14):c.125C>T (p.Pro42Leu)	not specified [RCV004623755]	uncertain significance	2	31137962	31137962	Human		name
407503450	CV3436288	single nucleotide variant	NM_054110.5(GALNT15):c.271C>T (p.Arg91Trp)	not specified [RCV004623761]	uncertain significance	3	16175422	16175422	Human		name
407503492	CV3436300	single nucleotide variant	NM_198516.3(GALNT18):c.268G>A (p.Glu90Lys)	not specified [RCV004623773]	uncertain significance	11	11448904	11448904	Human		name
597753668	CV3673542	single nucleotide variant	NM_198321.4(GALNT10):c.154G>C (p.Gly52Arg)	not specified [RCV004924190]	uncertain significance	5	154191020	154191020	Human		name
597753680	CV3673546	single nucleotide variant	NM_198321.4(GALNT10):c.296C>T (p.Thr99Ile)	not specified [RCV004924193]	uncertain significance	5	154297974	154297974	Human		name
597753698	CV3673550	single nucleotide variant	NM_022087.4(GALNT11):c.149C>T (p.Pro50Leu)	not specified [RCV004924197]	uncertain significance	7	152094376	152094376	Human		name
597779718	CV3673556	single nucleotide variant	NM_022087.4(GALNT11):c.206C>T (p.Pro69Leu)	not specified [RCV004930451]	uncertain significance	7	152094433	152094433	Human		name
597753714	CV3673557	single nucleotide variant	NM_022087.4(GALNT11):c.172C>T (p.Arg58Cys)	not specified [RCV004924201]	uncertain significance	7	152094399	152094399	Human		name
597753719	CV3673559	single nucleotide variant	NM_022087.4(GALNT11):c.197T>C (p.Val66Ala)	not specified [RCV004924202]	uncertain significance	7	152094424	152094424	Human		name
597753723	CV3673560	single nucleotide variant	NM_022087.4(GALNT11):c.241G>A (p.Asp81Asn)	not specified [RCV004924203]	uncertain significance	7	152094468	152094468	Human		name
597779729	CV3673569	single nucleotide variant	NM_024642.5(GALNT12):c.1152T>G (p.Ala384=)	not specified [RCV004930454]	likely benign	9	98837088	98837088	Human		name
597753764	CV3673575	single nucleotide variant	NM_024642.5(GALNT12):c.124G>A (p.Gly42Arg)	not specified [RCV004924213]	uncertain significance	9	98807822	98807822	Human		name
597753777	CV3673579	single nucleotide variant	NM_024642.5(GALNT12):c.245T>A (p.Val82Glu)	not specified [RCV004924216]	uncertain significance	9	98807943	98807943	Human		name
597753798	CV3673586	single nucleotide variant	NM_024642.5(GALNT12):c.197C>G (p.Pro66Arg)	not specified [RCV004924221]	uncertain significance	9	98807895	98807895	Human		name
597779759	CV3673589	single nucleotide variant	NM_024642.5(GALNT12):c.255G>T (p.Gln85His)	not specified [RCV004930461]	uncertain significance	9	98807953	98807953	Human		name
597753819	CV3673594	single nucleotide variant	NM_024642.5(GALNT12):c.200G>T (p.Arg67Leu)	not specified [RCV004924226]	uncertain significance	9	98807898	98807898	Human		name
597779776	CV3673601	single nucleotide variant	NM_024642.5(GALNT12):c.1656G>A (p.Arg552=)	not specified [RCV004930465]	likely benign	9	98849002	98849002	Human		name
597779784	CV3673607	single nucleotide variant	NM_024642.5(GALNT12):c.1545C>T (p.Thr515=)	not specified [RCV004930467]	likely benign	9	98846063	98846063	Human		name
597779818	CV3673616	single nucleotide variant	NM_024642.5(GALNT12):c.1426C>T (p.Leu476=)	not specified [RCV004930475]	likely benign	9	98844177	98844177	Human		name
597753878	CV3673621	single nucleotide variant	NM_024642.5(GALNT12):c.272T>C (p.Leu91Pro)	not specified [RCV004924240]	uncertain significance	9	98807970	98807970	Human		name
597779828	CV3673625	single nucleotide variant	NM_024642.5(GALNT12):c.233G>T (p.Arg78Leu)	not specified [RCV004930477]	uncertain significance	9	98807931	98807931	Human		name
597779832	CV3673626	single nucleotide variant	NM_024642.5(GALNT12):c.1011A>T (p.Gly337=)	not specified [RCV004930478]	likely benign	9	98835342	98835342	Human		name
597753893	CV3673628	single nucleotide variant	NM_024642.5(GALNT12):c.1080T>C (p.His360=)	not specified [RCV004924244]	likely benign	9	98837016	98837016	Human		name
597779840	CV3673629	single nucleotide variant	NM_024642.5(GALNT12):c.1692A>C (p.Arg564=)	not specified [RCV004930480]	likely benign	9	98849038	98849038	Human		name
597779847	CV3673631	single nucleotide variant	NM_024642.5(GALNT12):c.221C>T (p.Ala74Val)	not specified [RCV004930482]	uncertain significance	9	98807919	98807919	Human		name
597779856	CV3673634	single nucleotide variant	NM_024642.5(GALNT12):c.147G>C (p.Glu49Asp)	not specified [RCV004930484]	likely benign	9	98807845	98807845	Human		name
597779882	CV3673649	single nucleotide variant	NM_054110.5(GALNT15):c.187G>A (p.Glu63Lys)	not specified [RCV004930490]	uncertain significance	3	16175338	16175338	Human		name
597684389	CV3731207	single nucleotide variant	NM_024642.5(GALNT12):c.227G>A (p.Gly76Asp)	not provided [RCV004999039]	uncertain significance	9	98807925	98807925	Human		name
597887122	CV3787543	deletion	NM_024642.5(GALNT12):c.562del (p.Ala188fs)	not provided [RCV005125109]	uncertain significance	9	98826771	98826771	Human		name
597947560	CV3800729	single nucleotide variant	NM_024642.5(GALNT12):c.1611A>T (p.Gly537=)	not provided [RCV005135129]	likely benign	9	98848957	98848957	Human		name
598158853	CV3973861	single nucleotide variant	NM_024642.5(GALNT12):c.184G>C (p.Glu62Gln)	not specified [RCV005328147]	uncertain significance	9	98807882	98807882	Human		name
598202870	CV3973862	single nucleotide variant	NM_024642.5(GALNT12):c.131G>T (p.Gly44Val)	not specified [RCV005337170]	uncertain significance	9	98807829	98807829	Human		name
598202890	CV3973865	single nucleotide variant	NM_024642.5(GALNT12):c.1128T>C (p.Ala376=)	not specified [RCV005337173]	likely benign	9	98837064	98837064	Human		name
598202948	CV3973873	single nucleotide variant	NM_052917.4(GALNT13):c.228G>T (p.Glu76Asp)	not specified [RCV005337181]	uncertain significance	2	154140422	154140422	Human		name
598202973	CV3973877	single nucleotide variant	NM_052917.4(GALNT13):c.104A>G (p.Asp35Gly)	not specified [RCV005337185]	uncertain significance	2	153944601	153944601	Human		name
598202998	CV3973881	single nucleotide variant	NM_024572.4(GALNT14):c.223A>G (p.Lys75Glu)	not specified [RCV005337189]	uncertain significance	2	30992914	30992914	Human		name
598158858	CV3973898	single nucleotide variant	NM_022479.3(GALNT17):c.156C>A (p.Ser52Arg)	not specified [RCV005328148]	uncertain significance	7	71132958	71132958	Human		name
598203181	CV3973909	single nucleotide variant	NM_198516.3(GALNT18):c.286T>C (p.Ser96Pro)	not specified [RCV005337216]	uncertain significance	11	11448886	11448886	Human		name
598203187	CV3973910	single nucleotide variant	NM_198516.3(GALNT18):c.265G>T (p.Ala89Ser)	not specified [RCV005337217]	uncertain significance	11	11448907	11448907	Human		name
12898076	CV397508	single nucleotide variant	NM_024642.5(GALNT12):c.1638A>G (p.Lys546=)	not provided [RCV000471708]\|not specified [RCV004022803]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	9	98848984	98848984	Human		name
598202649	CV3977596	single nucleotide variant	NM_198321.4(GALNT10):c.155G>C (p.Gly52Ala)	not specified [RCV005337136]	uncertain significance	5	154191021	154191021	Human		name
598202657	CV3977597	single nucleotide variant	NM_198321.4(GALNT10):c.221G>C (p.Trp74Ser)	not specified [RCV005337137]	uncertain significance	5	154294877	154294877	Human		name
598202666	CV3977598	single nucleotide variant	NM_198321.4(GALNT10):c.185C>G (p.Thr62Arg)	not specified [RCV005337138]	uncertain significance	5	154294841	154294841	Human		name
598202680	CV3977600	single nucleotide variant	NM_022087.4(GALNT11):c.282C>A (p.Phe94Leu)	not specified [RCV005337140]	uncertain significance	7	152094509	152094509	Human		name
598158836	CV3977602	single nucleotide variant	NM_022087.4(GALNT11):c.113A>C (p.Lys38Thr)	not specified [RCV005328142]	uncertain significance	7	152094340	152094340	Human		name
598202708	CV3977605	single nucleotide variant	NM_024642.5(GALNT12):c.1032T>C (p.Phe344=)	not specified [RCV005337144]	likely benign	9	98835363	98835363	Human		name
598202859	CV3977632	single nucleotide variant	NM_024642.5(GALNT12):c.1056T>C (p.Val352=)	not specified [RCV005337168]	likely benign	9	98836992	98836992	Human		name
598189404	CV4008696	single nucleotide variant	NM_024642.5(GALNT12):c.100G>A (p.Gly34Ser)	Colorectal cancer, susceptibility to, 1 [RCV005396195]	uncertain significance	9	98807798	98807798	Human	1	name
598189520	CV4008711	single nucleotide variant	NM_024642.5(GALNT12):c.106G>A (p.Val36Met)	Colorectal cancer, susceptibility to, 1 [RCV005396210]	uncertain significance	9	98807804	98807804	Human	1	name
598189871	CV4008756	single nucleotide variant	NM_024642.5(GALNT12):c.161G>A (p.Arg54His)	Colorectal cancer, susceptibility to, 1 [RCV005396255]	uncertain significance	9	98807859	98807859	Human	1	name
598190020	CV4008778	single nucleotide variant	NM_024642.5(GALNT12):c.250C>A (p.Leu84Met)	Colorectal cancer, susceptibility to, 1 [RCV005396277]	uncertain significance	9	98807948	98807948	Human	1	name
616937882	CV4013798	deletion	NM_024642.5(GALNT12):c.771del (p.Ile257fs)	Colorectal cancer, susceptibility to, 1 [RCV005413290]	uncertain significance	9	98831810	98831810	Human	1	name
13496224	CV474979	single nucleotide variant	NM_024642.5(GALNT12):c.188C>A (p.Pro63Gln)	not provided [RCV001853773]\|not specified [RCV004024539]	uncertain significance	9	98807886	98807886	Human		name
13464709	CV474985	single nucleotide variant	NM_024642.5(GALNT12):c.193A>T (p.Met65Leu)	not provided [RCV003478289]\|not specified [RCV004024562]	likely benign\|uncertain significance	9	98807891	98807891	Human		name
13489850	CV475033	single nucleotide variant	NM_024642.5(GALNT12):c.1131G>A (p.Leu377=)	Colorectal cancer, susceptibility to, 1 [RCV005398911]\|not provided [RCV000862896]\|not specified [RCV004024522]	benign\|likely benign	9	98837067	98837067	Human	1	name
13477724	CV475036	single nucleotide variant	NM_024642.5(GALNT12):c.164C>T (p.Thr55Ile)	not provided [RCV001056163]\|not specified [RCV004599224]	likely benign\|uncertain significance	9	98807862	98807862	Human		name
13504094	CV475043	single nucleotide variant	NM_024642.5(GALNT12):c.1515C>T (p.Gly505=)	not provided [RCV002060517]\|not specified [RCV004024555]	likely benign	9	98846033	98846033	Human		name
13488576	CV475179	single nucleotide variant	NM_024642.5(GALNT12):c.139G>A (p.Ala47Thr)	Colorectal cancer, susceptibility to, 1 [RCV003465260]\|not provided [RCV001235145]\|not specified [RCV004599225]	likely benign\|uncertain significance	9	98807837	98807837	Human	1	name
13472208	CV475198	single nucleotide variant	NM_024642.5(GALNT12):c.212C>T (p.Pro71Leu)	Colorectal cancer, susceptibility to, 1 [RCV003459383]\|not provided [RCV000794002]\|not specified [RCV004024546]	uncertain significance	9	98807910	98807910	Human	1	name
13467328	CV475200	single nucleotide variant	NM_024642.5(GALNT12):c.214G>T (p.Ala72Ser)	not provided [RCV001218768]\|not specified [RCV004024530]	uncertain significance	9	98807912	98807912	Human		name
13482810	CV475201	single nucleotide variant	NM_024642.5(GALNT12):c.262G>A (p.Gly88Ser)	not specified [RCV004024563]	uncertain significance	9	98807960	98807960	Human		name
13470427	CV475202	single nucleotide variant	NM_024642.5(GALNT12):c.1338C>T (p.Phe446=)	not provided [RCV003669154]\|not specified [RCV004024549]	likely benign	9	98840127	98840127	Human		name
13502245	CV475203	single nucleotide variant	NM_024642.5(GALNT12):c.1581G>A (p.Glu527=)	not provided [RCV000870406]\|not specified [RCV004024524]	likely benign\|conflicting interpretations of pathogenicity	9	98846099	98846099	Human		name
13500157	CV475209	single nucleotide variant	NM_024642.5(GALNT12):c.1599G>A (p.Leu533=)	not provided [RCV003478288]\|not specified [RCV004024561]	likely benign	9	98846117	98846117	Human		name
13471794	CV475233	single nucleotide variant	NM_024642.5(GALNT12):c.1707G>C (p.Ser569=)	Hereditary cancer-predisposing syndrome [RCV005055019]\|not provided [RCV001509818]\|not specified [RCV004024518]	benign	9	98849053	98849053	Human	1	name
14702680	CV638616	single nucleotide variant	NM_024642.5(GALNT12):c.104C>T (p.Ser35Leu)	Colorectal cancer, susceptibility to, 1 [RCV003461166]\|not provided [RCV000807069]\|not specified [RCV004028275]	uncertain significance	9	98807802	98807802	Human	1	name
14731500	CV638619	single nucleotide variant	NM_024642.5(GALNT12):c.206C>T (p.Pro69Leu)	not provided [RCV000817854]\|not specified [RCV004028928]	uncertain significance	9	98807904	98807904	Human		name
15100906	CV687574	single nucleotide variant	NM_024642.5(GALNT12):c.1020C>T (p.Leu340=)	not provided [RCV000870144]\|not specified [RCV004027770]	likely benign	9	98835351	98835351	Human		name
15098470	CV687576	single nucleotide variant	NM_024642.5(GALNT12):c.1584T>C (p.Asn528=)	not provided [RCV000869706]\|not specified [RCV004027759]	likely benign	9	98846102	98846102	Human		name
15098813	CV687577	single nucleotide variant	NM_024642.5(GALNT12):c.1608T>C (p.Asp536=)	not provided [RCV000869785]\|not specified [RCV004027761]	likely benign	9	98848954	98848954	Human		name
15156286	CV687578	single nucleotide variant	NM_024642.5(GALNT12):c.1707G>A (p.Ser569=)	not provided [RCV000868202]\|not specified [RCV004027716]	benign\|likely benign	9	98849053	98849053	Human		name
15148408	CV687579	single nucleotide variant	NM_024642.5(GALNT12):c.1743A>G (p.Leu581=)	not provided [RCV000866657]\|not specified [RCV004027676]	likely benign	9	98849089	98849089	Human		name
15116322	CV692750	single nucleotide variant	NM_024642.5(GALNT12):c.1044G>A (p.Gln348=)	not provided [RCV000873304]\|not specified [RCV004027821]	likely benign	9	98836980	98836980	Human		name
15140367	CV692751	single nucleotide variant	NM_024642.5(GALNT12):c.1359A>G (p.Gly453=)	not provided [RCV000877485]\|not specified [RCV004027890]	likely benign	9	98844110	98844110	Human		name
15140143	CV692752	single nucleotide variant	NM_024642.5(GALNT12):c.1440T>C (p.His480=)	not provided [RCV000877440]\|not specified [RCV004027888]	likely benign	9	98844191	98844191	Human		name
15196959	CV698980	single nucleotide variant	NM_198321.4(GALNT10):c.1626G>A (p.Lys542=)	not provided [RCV000956332]	benign	5	154415905	154415905	Human		name
15179307	CV701127	single nucleotide variant	NM_024642.5(GALNT12):c.1083T>C (p.Val361=)	not provided [RCV000951488]	likely benign	9	98837019	98837019	Human		name
15179494	CV701128	single nucleotide variant	NM_024642.5(GALNT12):c.1653G>A (p.Ala551=)	not provided [RCV000951532]\|not specified [RCV004029825]	likely benign	9	98848999	98848999	Human		name
15164846	CV708230	single nucleotide variant	NM_024572.4(GALNT14):c.1494C>T (p.Asp498=)	not provided [RCV000970819]	benign	2	30912229	30912229	Human		name
15164849	CV708231	single nucleotide variant	NM_024572.4(GALNT14):c.205G>A (p.Val69Ile)	not provided [RCV000970820]	benign	2	30992932	30992932	Human		name
15182262	CV712101	single nucleotide variant	NM_024642.5(GALNT12):c.1203T>C (p.Arg401=)	not provided [RCV000974589]\|not specified [RCV004029984]	likely benign	9	98837139	98837139	Human		name
15109631	CV712102	single nucleotide variant	NM_024642.5(GALNT12):c.1227T>C (p.Asp409=)	not provided [RCV000960740]\|not specified [RCV004029891]	likely benign	9	98840016	98840016	Human		name
15163956	CV723699	single nucleotide variant	NM_024642.5(GALNT12):c.1503C>T (p.His501=)	not provided [RCV000882089]	likely benign	9	98846021	98846021	Human		name
15173967	CV723700	single nucleotide variant	NM_024642.5(GALNT12):c.1521T>A (p.Ile507=)	not provided [RCV000884087]	likely benign	9	98846039	98846039	Human		name
15146152	CV750736	single nucleotide variant	NM_022479.3(GALNT17):c.1260G>A (p.Pro420=)	not provided [RCV000922671]	benign	7	71665590	71665590	Human		name
15198006	CV751880	single nucleotide variant	NM_024642.5(GALNT12):c.1110C>A (p.Pro370=)	not provided [RCV000912134]\|not specified [RCV004029352]	likely benign	9	98837046	98837046	Human		name
15146259	CV751881	single nucleotide variant	NM_024642.5(GALNT12):c.1395T>C (p.Asp465=)	not provided [RCV000922689]\|not specified [RCV004029480]	likely benign	9	98844146	98844146	Human		name
15180022	CV767578	single nucleotide variant	NM_024642.5(GALNT12):c.1029C>T (p.Ser343=)	not provided [RCV000929784]\|not specified [RCV004029555]	likely benign	9	98835360	98835360	Human		name
8625352	CV80475	single nucleotide variant	NM_024572.3(GALNT14):c.1338G>A (p.Leu446=)	Malignant melanoma [RCV000060552]	not provided	2	30924161	30924161	Human		name
25323999	CV809679	single nucleotide variant	NM_024642.5(GALNT12):c.134C>G (p.Ala45Gly)	not specified [RCV004030309]	uncertain significance	9	98807832	98807832	Human		name
25324929	CV809682	single nucleotide variant	NM_024642.5(GALNT12):c.149C>A (p.Pro50Gln)	not provided [RCV001039732]\|not specified [RCV004030332]	likely benign\|uncertain significance	9	98807847	98807847	Human		name
25325200	CV809683	single nucleotide variant	NM_024642.5(GALNT12):c.155C>T (p.Pro52Leu)	Colorectal cancer, susceptibility to, 1 [RCV003461324]\|not provided [RCV003478613]\|not specified [RCV004030335]	uncertain significance	9	98807853	98807853	Human	1	name
25325246	CV809685	single nucleotide variant	NM_024642.5(GALNT12):c.158C>A (p.Pro53Gln)	not specified [RCV004030336]	uncertain significance	9	98807856	98807856	Human		name
25325752	CV809687	single nucleotide variant	NM_024642.5(GALNT12):c.167C>T (p.Pro56Leu)	not provided [RCV001037263]\|not specified [RCV004030344]	uncertain significance	9	98807865	98807865	Human		name
25326265	CV809688	single nucleotide variant	NM_024642.5(GALNT12):c.178C>G (p.Arg60Gly)	not provided [RCV001303274]\|not specified [RCV004030354]	uncertain significance	9	98807876	98807876	Human		name
25326681	CV809689	single nucleotide variant	NM_024642.5(GALNT12):c.188C>G (p.Pro63Arg)	not specified [RCV004030357]	uncertain significance	9	98807886	98807886	Human		name
25326877	CV809691	single nucleotide variant	NM_024642.5(GALNT12):c.193A>C (p.Met65Leu)	not specified [RCV004030358]	likely benign	9	98807891	98807891	Human		name
25326878	CV809692	single nucleotide variant	NM_024642.5(GALNT12):c.193A>G (p.Met65Val)	not provided [RCV001219573]\|not specified [RCV004030359]	likely benign\|uncertain significance	9	98807891	98807891	Human		name
25327100	CV809693	single nucleotide variant	NM_024642.5(GALNT12):c.199C>T (p.Arg67Trp)	Colorectal cancer, susceptibility to, 1 [RCV003467614]\|not provided [RCV002549400]\|not specified [RCV004030361]	uncertain significance	9	98807897	98807897	Human	1	name
25327384	CV809694	single nucleotide variant	NM_024642.5(GALNT12):c.205C>G (p.Pro69Ala)	not provided [RCV001308613]\|not specified [RCV004030364]	uncertain significance	9	98807903	98807903	Human		name
25328205	CV809695	single nucleotide variant	NM_024642.5(GALNT12):c.235G>T (p.Gly79Cys)	not specified [RCV004030374]	uncertain significance	9	98807933	98807933	Human		name
25328659	CV809697	single nucleotide variant	NM_024642.5(GALNT12):c.263G>T (p.Gly88Val)	not provided [RCV002549433]\|not specified [RCV004030380]	uncertain significance	9	98807961	98807961	Human		name
25328646	CV809698	single nucleotide variant	NM_024642.5(GALNT12):c.265G>T (p.Glu89Ter)	Colorectal cancer, susceptibility to, 1 [RCV005394631]\|not provided [RCV001860819]\|not specified [RCV004030379]	uncertain significance	9	98807963	98807963	Human	1	name
25329157	CV809762	single nucleotide variant	NM_024642.5(GALNT12):c.1068C>T (p.His356=)	not specified [RCV004030391]	likely benign	9	98837004	98837004	Human		name
25323858	CV809775	single nucleotide variant	NM_024642.5(GALNT12):c.1306C>T (p.Leu436=)	not specified [RCV004030306]	likely benign	9	98840095	98840095	Human		name
25323777	CV809778	single nucleotide variant	NM_024642.5(GALNT12):c.1335C>T (p.Phe445=)	not specified [RCV004030303]	likely benign	9	98840124	98840124	Human		name
25324505	CV809783	single nucleotide variant	NM_024642.5(GALNT12):c.1428G>C (p.Leu476=)	not provided [RCV002068836]\|not specified [RCV004030320]	likely benign	9	98844179	98844179	Human		name
25324617	CV809784	single nucleotide variant	NM_024642.5(GALNT12):c.1443G>A (p.Gly481=)	not provided [RCV005093077]\|not specified [RCV004030325]	likely benign	9	98844194	98844194	Human		name
25324829	CV809786	single nucleotide variant	NM_024642.5(GALNT12):c.1482A>G (p.Lys494=)	not specified [RCV004030327]	likely benign	9	98846000	98846000	Human		name
25324871	CV809789	single nucleotide variant	NM_024642.5(GALNT12):c.1491C>T (p.Arg497=)	not provided [RCV002068844]\|not specified [RCV004030329]	likely benign	9	98846009	98846009	Human		name
25326053	CV809804	single nucleotide variant	NM_024642.5(GALNT12):c.1734G>A (p.Glu578=)	not specified [RCV004030352]	likely benign	9	98849080	98849080	Human		name
26904781	CV836489	single nucleotide variant	NM_024642.5(GALNT12):c.154C>T (p.Pro52Ser)	not provided [RCV001071131]\|not specified [RCV004599242]	likely benign\|uncertain significance	9	98807852	98807852	Human		name
26904565	CV836491	single nucleotide variant	NM_024642.5(GALNT12):c.226G>A (p.Gly76Ser)	Colorectal cancer, susceptibility to, 1 [RCV004570306]\|not provided [RCV001070873]\|not specified [RCV004030764]	uncertain significance	9	98807924	98807924	Human	1	name
8630315	CV85470	single nucleotide variant	NM_024572.3(GALNT14):c.1449C>T (p.Phe483=)	Malignant melanoma [RCV000065553]	not provided	2	30912274	30912274	Human		name
38474909	CV934886	single nucleotide variant	NM_024642.5(GALNT12):c.175G>C (p.Gly59Arg)	not provided [RCV001204016]	uncertain significance	9	98807873	98807873	Human		name
38473087	CV934887	single nucleotide variant	NM_024642.5(GALNT12):c.251T>C (p.Leu84Pro)	Colorectal cancer, susceptibility to, 1 [RCV005394812]\|not provided [RCV001203372]\|not specified [RCV004033569]	uncertain significance	9	98807949	98807949	Human	1	name
38457389	CV946757	single nucleotide variant	NM_024642.5(GALNT12):c.268G>A (p.Glu90Lys)	not provided [RCV001228653]\|not specified [RCV004032644]	uncertain significance	9	98807966	98807966	Human		name
126744527	CV993621	single nucleotide variant	NM_024642.5(GALNT12):c.140C>A (p.Ala47Asp)	Colorectal cancer, susceptibility to, 1 [RCV005040137]\|not provided [RCV001296349]\|not specified [RCV004036029]	uncertain significance	9	98807838	98807838	Human	1	name
126758109	CV993633	single nucleotide variant	NM_024642.5(GALNT12):c.1690C>A (p.Arg564=)	not provided [RCV001299088]\|not specified [RCV004036126]	likely benign\|uncertain significance	9	98849036	98849036	Human		name
405749050	CV3254377	single nucleotide variant	NM_052917.4(GALNT13):c.986G>A (p.Cys329Tyr)	not specified [RCV004392456]	uncertain significance	2	154301419	154301419	Human		name
405749237	CV3254404	single nucleotide variant	NM_054110.5(GALNT15):c.301T>G (p.Leu101Val)	not specified [RCV004392483]	uncertain significance	3	16175452	16175452	Human		name
405749244	CV3254405	single nucleotide variant	NM_054110.5(GALNT15):c.353G>A (p.Arg118His)	not specified [RCV004392484]	uncertain significance	3	16175504	16175504	Human		name
405749250	CV3254406	single nucleotide variant	NM_054110.5(GALNT15):c.449C>T (p.Thr150Ile)	not specified [RCV004392485]	uncertain significance	3	16175600	16175600	Human		name
405749273	CV3254409	single nucleotide variant	NM_054110.5(GALNT15):c.625C>T (p.Arg209Trp)	not specified [RCV004392488]	uncertain significance	3	16195845	16195845	Human		name
405749279	CV3254410	single nucleotide variant	NM_054110.5(GALNT15):c.626G>A (p.Arg209Gln)	not specified [RCV004392489]	uncertain significance	3	16195846	16195846	Human		name
405749285	CV3254411	single nucleotide variant	NM_054110.5(GALNT15):c.707G>A (p.Gly236Glu)	not specified [RCV004392490]	uncertain significance	3	16200619	16200619	Human		name
405749292	CV3254412	single nucleotide variant	NM_054110.5(GALNT15):c.724C>G (p.Leu242Val)	not specified [RCV004392491]	uncertain significance	3	16200636	16200636	Human		name
405749299	CV3254413	single nucleotide variant	NM_054110.5(GALNT15):c.929C>T (p.Pro310Leu)	not specified [RCV004392492]	uncertain significance	3	16208520	16208520	Human		name
405749480	CV3254438	single nucleotide variant	NM_022479.3(GALNT17):c.398C>G (p.Ser133Cys)	not specified [RCV004392518]	uncertain significance	7	71335709	71335709	Human		name
405749486	CV3254439	single nucleotide variant	NM_022479.3(GALNT17):c.497C>T (p.Ser166Leu)	not specified [RCV004392519]	uncertain significance	7	71388309	71388309	Human		name
405749493	CV3254440	single nucleotide variant	NM_022479.3(GALNT17):c.526G>A (p.Val176Ile)	not specified [RCV004392520]	uncertain significance	7	71388338	71388338	Human		name
405749500	CV3254441	single nucleotide variant	NM_022479.3(GALNT17):c.634C>T (p.Pro212Ser)	not specified [RCV004392521]	uncertain significance	7	71415933	71415933	Human		name
405749509	CV3254442	single nucleotide variant	NM_022479.3(GALNT17):c.637G>A (p.Gly213Arg)	not specified [RCV004392522]	uncertain significance	7	71415936	71415936	Human		name
405749518	CV3254443	single nucleotide variant	NM_022479.3(GALNT17):c.649G>A (p.Val217Met)	not specified [RCV004392523]	uncertain significance	7	71415948	71415948	Human		name
405749534	CV3254445	single nucleotide variant	NM_022479.3(GALNT17):c.713C>G (p.Thr238Ser)	not specified [RCV004392525]	uncertain significance	7	71416012	71416012	Human		name
405749541	CV3254446	single nucleotide variant	NM_022479.3(GALNT17):c.785G>A (p.Arg262His)	not specified [RCV004392526]	uncertain significance	7	71420928	71420928	Human		name
405749548	CV3254447	single nucleotide variant	NM_022479.3(GALNT17):c.820T>G (p.Ser274Ala)	not specified [RCV004392527]	uncertain significance	7	71420963	71420963	Human		name
405749602	CV3254455	single nucleotide variant	NM_198516.3(GALNT18):c.334G>A (p.Val112Met)	not specified [RCV004392535]	uncertain significance	11	11448838	11448838	Human		name
405749609	CV3254456	single nucleotide variant	NM_198516.3(GALNT18):c.578A>G (p.Asp193Gly)	not specified [RCV004392536]	uncertain significance	11	11432638	11432638	Human		name
405868873	CV3400640	single nucleotide variant	NM_024642.5(GALNT12):c.368C>G (p.Pro123Arg)	Colorectal cancer, susceptibility to, 1 [RCV004576643]	uncertain significance	9	98808066	98808066	Human	1	name
405868881	CV3400643	single nucleotide variant	NM_024642.5(GALNT12):c.656C>G (p.Ala219Gly)	Colorectal cancer, susceptibility to, 1 [RCV004576646]	uncertain significance	9	98826866	98826866	Human	1	name
405868889	CV3400646	deletion	NM_024642.5(GALNT12):c.1732del (p.Glu578fs)	Colorectal cancer, susceptibility to, 1 [RCV004576649]	uncertain significance	9	98849078	98849078	Human	1	name
407486936	CV3436208	single nucleotide variant	NM_022087.4(GALNT11):c.917C>T (p.Pro306Leu)	not specified [RCV004619181]	uncertain significance	7	152108242	152108242	Human		name
407486942	CV3436209	single nucleotide variant	NM_022087.4(GALNT11):c.701C>T (p.Ala234Val)	not specified [RCV004619182]	uncertain significance	7	152105359	152105359	Human		name
407486954	CV3436211	single nucleotide variant	NM_022087.4(GALNT11):c.838G>A (p.Asp280Asn)	not specified [RCV004619184]	uncertain significance	7	152108163	152108163	Human		name
407503184	CV3436215	single nucleotide variant	NM_022087.4(GALNT11):c.611A>G (p.Glu204Gly)	not specified [RCV004623688]	uncertain significance	7	152105269	152105269	Human		name
407503221	CV3436225	single nucleotide variant	NM_024642.5(GALNT12):c.781G>T (p.Asp261Tyr)	not specified [RCV004623698]	uncertain significance	9	98831821	98831821	Human		name
407503246	CV3436232	single nucleotide variant	NM_024642.5(GALNT12):c.571C>A (p.Leu191Ile)	not specified [RCV004623705]	uncertain significance	9	98826781	98826781	Human		name
407503260	CV3436236	single nucleotide variant	NM_024642.5(GALNT12):c.386A>T (p.Lys129Ile)	not specified [RCV004623709]	uncertain significance	9	98823270	98823270	Human		name
407503284	CV3436242	single nucleotide variant	NM_024642.5(GALNT12):c.796G>C (p.Glu266Gln)	not specified [RCV004623715]	uncertain significance	9	98831836	98831836	Human		name
407503304	CV3436248	single nucleotide variant	NM_024642.5(GALNT12):c.490C>G (p.Pro164Ala)	not specified [RCV004623721]	uncertain significance	9	98823374	98823374	Human		name
407503312	CV3436250	single nucleotide variant	NM_024642.5(GALNT12):c.872C>T (p.Pro291Leu)	not specified [RCV004623723]	uncertain significance	9	98831912	98831912	Human		name
407503341	CV3436258	single nucleotide variant	NM_024642.5(GALNT12):c.931G>A (p.Ala311Thr)	not specified [RCV004623731]	uncertain significance	9	98835262	98835262	Human		name
407503385	CV3436270	single nucleotide variant	NM_024642.5(GALNT12):c.554A>T (p.Glu185Val)	not specified [RCV004623743]	uncertain significance	9	98826764	98826764	Human		name
407503392	CV3436272	single nucleotide variant	NM_024642.5(GALNT12):c.764C>G (p.Pro255Arg)	not specified [RCV004623745]	uncertain significance	9	98831804	98831804	Human		name
407503402	CV3436275	single nucleotide variant	NM_052917.4(GALNT13):c.919A>T (p.Thr307Ser)	not specified [RCV004623748]	uncertain significance	2	154259082	154259082	Human		name
407503413	CV3436278	single nucleotide variant	NM_024572.4(GALNT14):c.856G>A (p.Val286Met)	not specified [RCV004623751]	uncertain significance	2	30942276	30942276	Human		name
407503416	CV3436279	single nucleotide variant	NM_024572.4(GALNT14):c.371G>A (p.Arg124His)	not specified [RCV004623752]	uncertain significance	2	30966231	30966231	Human		name
407503419	CV3436280	single nucleotide variant	NM_024572.4(GALNT14):c.503T>G (p.Val168Gly)	not specified [RCV004623753]	uncertain significance	2	30955941	30955941	Human		name
407503424	CV3436281	single nucleotide variant	NM_024572.4(GALNT14):c.568G>T (p.Ala190Ser)	not specified [RCV004623754]	uncertain significance	2	30955704	30955704	Human		name
407503433	CV3436284	single nucleotide variant	NM_054110.5(GALNT15):c.812C>T (p.Ala271Val)	not specified [RCV004623757]	uncertain significance	3	16200724	16200724	Human		name
407503437	CV3436285	single nucleotide variant	NM_054110.5(GALNT15):c.355C>T (p.Leu119Phe)	not specified [RCV004623758]	uncertain significance	3	16175506	16175506	Human		name
407503477	CV3436296	single nucleotide variant	NM_022479.3(GALNT17):c.629G>A (p.Arg210His)	not specified [RCV004623769]	uncertain significance	7	71415928	71415928	Human		name
407503486	CV3436298	single nucleotide variant	NM_198516.3(GALNT18):c.671G>A (p.Arg224His)	not specified [RCV004623771]	uncertain significance	11	11379189	11379189	Human		name
597779697	CV3673538	single nucleotide variant	NM_198321.4(GALNT10):c.994C>T (p.Leu332Phe)	not specified [RCV004930446]	uncertain significance	5	154386368	154386368	Human		name
597753659	CV3673539	single nucleotide variant	NM_198321.4(GALNT10):c.893C>T (p.Pro298Leu)	not specified [RCV004924188]	uncertain significance	5	154380586	154380586	Human		name
597779700	CV3673540	single nucleotide variant	NM_198321.4(GALNT10):c.814G>A (p.Asp272Asn)	not specified [RCV004930447]	uncertain significance	5	154380507	154380507	Human		name
597753663	CV3673541	single nucleotide variant	NM_198321.4(GALNT10):c.313G>A (p.Asp105Asn)	not specified [RCV004924189]	uncertain significance	5	154297991	154297991	Human		name
597753672	CV3673543	single nucleotide variant	NM_198321.4(GALNT10):c.838G>T (p.Ala280Ser)	not specified [RCV004924191]	uncertain significance	5	154380531	154380531	Human		name
597753689	CV3673548	single nucleotide variant	NM_198321.4(GALNT10):c.389T>C (p.Ile130Thr)	not specified [RCV004924195]	uncertain significance	5	154298067	154298067	Human		name
597753702	CV3673551	single nucleotide variant	NM_022087.4(GALNT11):c.698C>T (p.Ala233Val)	not specified [RCV004924198]	uncertain significance	7	152105356	152105356	Human		name
597779708	CV3673552	single nucleotide variant	NM_022087.4(GALNT11):c.613T>C (p.Tyr205His)	not specified [RCV004930449]	uncertain significance	7	152105271	152105271	Human		name
597779723	CV3673558	single nucleotide variant	NM_022087.4(GALNT11):c.458C>G (p.Ala153Gly)	not specified [RCV004930452]	uncertain significance	7	152103150	152103150	Human		name
597753727	CV3673561	single nucleotide variant	NM_022087.4(GALNT11):c.308A>C (p.Asn103Thr)	not specified [RCV004924204]	uncertain significance	7	152100810	152100810	Human		name
597753773	CV3673577	single nucleotide variant	NM_024642.5(GALNT12):c.692G>T (p.Cys231Phe)	not specified [RCV004924215]	uncertain significance	9	98826902	98826902	Human		name
597753794	CV3673585	single nucleotide variant	NM_024642.5(GALNT12):c.569A>G (p.Glu190Gly)	not specified [RCV004924220]	uncertain significance	9	98826779	98826779	Human		name
597753802	CV3673587	single nucleotide variant	NM_024642.5(GALNT12):c.803T>C (p.Leu268Pro)	not specified [RCV004924222]	uncertain significance	9	98831843	98831843	Human		name
597753828	CV3673597	single nucleotide variant	NM_024642.5(GALNT12):c.518T>C (p.Leu173Pro)	not specified [RCV004924228]	uncertain significance	9	98823402	98823402	Human		name
597753832	CV3673598	single nucleotide variant	NM_024642.5(GALNT12):c.298C>A (p.Leu100Met)	not specified [RCV004924229]	uncertain significance	9	98807996	98807996	Human		name
597753845	CV3673602	single nucleotide variant	NM_024642.5(GALNT12):c.553G>A (p.Glu185Lys)	not specified [RCV004924232]	uncertain significance	9	98826763	98826763	Human		name
597753852	CV3673605	single nucleotide variant	NM_024642.5(GALNT12):c.449C>T (p.Ser150Leu)	not specified [RCV004924234]	uncertain significance	9	98823333	98823333	Human		name
597779796	CV3673611	single nucleotide variant	NM_024642.5(GALNT12):c.989C>A (p.Thr330Lys)	not specified [RCV004930470]	uncertain significance	9	98835320	98835320	Human		name
597779802	CV3673612	single nucleotide variant	NM_024642.5(GALNT12):c.328C>A (p.Arg110Ser)	not specified [RCV004930471]	uncertain significance	9	98808026	98808026	Human		name
597753866	CV3673618	single nucleotide variant	NM_024642.5(GALNT12):c.319C>G (p.Leu107Val)	not specified [RCV004924237]	uncertain significance	9	98808017	98808017	Human		name
597753870	CV3673619	single nucleotide variant	NM_024642.5(GALNT12):c.752C>T (p.Ala251Val)	not specified [RCV004924238]	uncertain significance	9	98831792	98831792	Human		name
597753874	CV3673620	single nucleotide variant	NM_024642.5(GALNT12):c.882G>C (p.Glu294Asp)	not specified [RCV004924239]	uncertain significance	9	98831922	98831922	Human		name
597753886	CV3673623	single nucleotide variant	NM_024642.5(GALNT12):c.841T>C (p.Trp281Arg)	not specified [RCV004924242]	uncertain significance	9	98831881	98831881	Human		name
597753889	CV3673624	single nucleotide variant	NM_024642.5(GALNT12):c.832G>C (p.Gly278Arg)	not specified [RCV004924243]	uncertain significance	9	98831872	98831872	Human		name
597779865	CV3673637	single nucleotide variant	NM_052917.4(GALNT13):c.692C>T (p.Thr231Met)	not specified [RCV004930486]	uncertain significance	2	154245817	154245817	Human		name
597753906	CV3673638	single nucleotide variant	NM_052917.4(GALNT13):c.614C>T (p.Thr205Ile)	not specified [RCV004924247]	uncertain significance	2	154242833	154242833	Human		name
597779869	CV3673640	single nucleotide variant	NM_024572.4(GALNT14):c.815C>T (p.Thr272Met)	not specified [RCV004930487]	uncertain significance	2	30944870	30944870	Human		name
597753917	CV3673642	single nucleotide variant	NM_024572.4(GALNT14):c.490A>G (p.Lys164Glu)	not specified [RCV004924250]	uncertain significance	2	30955954	30955954	Human		name
597753923	CV3673643	single nucleotide variant	NM_024572.4(GALNT14):c.332C>T (p.Pro111Leu)	not specified [RCV004924251]	uncertain significance	2	30966270	30966270	Human		name
597779879	CV3673646	single nucleotide variant	NM_054110.5(GALNT15):c.982C>G (p.Leu328Val)	not specified [RCV004930489]	uncertain significance	3	16208573	16208573	Human		name
597753930	CV3673647	single nucleotide variant	NM_054110.5(GALNT15):c.449C>A (p.Thr150Asn)	not specified [RCV004924253]	uncertain significance	3	16175600	16175600	Human		name
597753977	CV3673664	single nucleotide variant	NM_022479.3(GALNT17):c.952C>G (p.Leu318Val)	not specified [RCV004924264]	uncertain significance	7	71421095	71421095	Human		name
597753989	CV3673670	single nucleotide variant	NM_198516.3(GALNT18):c.438C>G (p.Asn146Lys)	not specified [RCV004924267]	uncertain significance	11	11432778	11432778	Human		name
597754002	CV3673676	single nucleotide variant	NM_198516.3(GALNT18):c.452A>T (p.Asp151Val)	not specified [RCV004924270]	uncertain significance	11	11432764	11432764	Human		name
597779935	CV3680687	single nucleotide variant	NM_198516.3(GALNT18):c.800G>A (p.Arg267His)	not specified [RCV004930502]	uncertain significance	11	11377359	11377359	Human		name
597941074	CV3785707	single nucleotide variant	NM_024642.5(GALNT12):c.856A>G (p.Thr286Ala)	not provided [RCV005133599]	uncertain significance	9	98831896	98831896	Human		name
597938709	CV3788335	single nucleotide variant	NM_024642.5(GALNT12):c.932C>T (p.Ala311Val)	not provided [RCV005133010]	uncertain significance	9	98835263	98835263	Human		name
597974278	CV3801868	single nucleotide variant	NM_024642.5(GALNT12):c.318C>G (p.Tyr106Ter)	not provided [RCV005143857]	uncertain significance	9	98808016	98808016	Human		name
597954661	CV3809303	single nucleotide variant	NM_024642.5(GALNT12):c.823C>T (p.Gln275Ter)	not provided [RCV005162027]	uncertain significance	9	98831863	98831863	Human		name
597929642	CV3837287	single nucleotide variant	NM_024642.5(GALNT12):c.871C>T (p.Pro291Ser)	not provided [RCV005185445]	uncertain significance	9	98831911	98831911	Human		name
597962680	CV3841056	single nucleotide variant	NM_024642.5(GALNT12):c.367C>A (p.Pro123Thr)	not provided [RCV005193349]	uncertain significance	9	98808065	98808065	Human		name
598202878	CV3973863	single nucleotide variant	NM_024642.5(GALNT12):c.755T>A (p.Val252Glu)	not specified [RCV005337171]	uncertain significance	9	98831795	98831795	Human		name
598202925	CV3973870	single nucleotide variant	NM_024642.5(GALNT12):c.760T>G (p.Cys254Gly)	not specified [RCV005337178]	uncertain significance	9	98831800	98831800	Human		name
598202932	CV3973871	single nucleotide variant	NM_024642.5(GALNT12):c.560T>C (p.Leu187Ser)	not specified [RCV005337179]	uncertain significance	9	98826770	98826770	Human		name
598202954	CV3973874	single nucleotide variant	NM_052917.4(GALNT13):c.317A>G (p.Lys106Arg)	not specified [RCV005337182]	uncertain significance	2	154242035	154242035	Human		name
598203005	CV3973882	single nucleotide variant	NM_024572.4(GALNT14):c.689T>C (p.Ile230Thr)	not specified [RCV005337190]	uncertain significance	2	30945836	30945836	Human		name
598203013	CV3973883	single nucleotide variant	NM_054110.5(GALNT15):c.826G>A (p.Gly276Arg)	not specified [RCV005337191]	uncertain significance	3	16200738	16200738	Human		name
598203026	CV3973885	single nucleotide variant	NM_054110.5(GALNT15):c.883C>G (p.Pro295Ala)	not specified [RCV005337193]	uncertain significance	3	16200795	16200795	Human		name
598203043	CV3973888	single nucleotide variant	NM_054110.5(GALNT15):c.737T>G (p.Val246Gly)	not specified [RCV005337196]	uncertain significance	3	16200649	16200649	Human		name
598203067	CV3973892	single nucleotide variant	NM_054110.5(GALNT15):c.737T>C (p.Val246Ala)	not specified [RCV005337200]	uncertain significance	3	16200649	16200649	Human		name
598203118	CV3973900	single nucleotide variant	NM_022479.3(GALNT17):c.852G>C (p.Glu284Asp)	not specified [RCV005337207]	uncertain significance	7	71420995	71420995	Human		name
598203125	CV3973901	single nucleotide variant	NM_022479.3(GALNT17):c.745G>A (p.Val249Met)	not specified [RCV005337208]	uncertain significance	7	71416044	71416044	Human		name
598203138	CV3973903	single nucleotide variant	NM_022479.3(GALNT17):c.986C>T (p.Ser329Leu)	not specified [RCV005337210]	uncertain significance	7	71571308	71571308	Human		name
598203153	CV3973905	single nucleotide variant	NM_198516.3(GALNT18):c.532A>G (p.Met178Val)	not specified [RCV005337212]	uncertain significance	11	11432684	11432684	Human		name
598203159	CV3973906	single nucleotide variant	NM_198516.3(GALNT18):c.799C>T (p.Arg267Cys)	not specified [RCV005337213]	uncertain significance	11	11377360	11377360	Human		name
598203194	CV3973911	single nucleotide variant	NM_198516.3(GALNT18):c.628G>A (p.Asp210Asn)	not specified [RCV005337218]	uncertain significance	11	11379232	11379232	Human		name
598202642	CV3977595	single nucleotide variant	NM_198321.4(GALNT10):c.349G>A (p.Val117Ile)	not specified [RCV005337135]	uncertain significance	5	154298027	154298027	Human		name
598202673	CV3977599	single nucleotide variant	NM_198321.4(GALNT10):c.873G>C (p.Glu291Asp)	not specified [RCV005337139]	uncertain significance	5	154380566	154380566	Human		name
598202700	CV3977604	single nucleotide variant	NM_022087.4(GALNT11):c.539C>T (p.Ala180Val)	not specified [RCV005337143]	uncertain significance	7	152103231	152103231	Human		name
598202737	CV3977611	single nucleotide variant	NM_024642.5(GALNT12):c.561G>C (p.Leu187Phe)	not specified [RCV005337149]	uncertain significance	9	98826771	98826771	Human		name
598202744	CV3977612	single nucleotide variant	NM_024642.5(GALNT12):c.413C>G (p.Thr138Arg)	not specified [RCV005337150]	uncertain significance	9	98823297	98823297	Human		name
598202757	CV3977614	single nucleotide variant	NM_024642.5(GALNT12):c.452C>T (p.Thr151Ile)	not specified [RCV005337152]	uncertain significance	9	98823336	98823336	Human		name
598202784	CV3977618	single nucleotide variant	NM_024642.5(GALNT12):c.825G>C (p.Gln275His)	not specified [RCV005337156]	uncertain significance	9	98831865	98831865	Human		name
598158842	CV3977619	single nucleotide variant	NM_024642.5(GALNT12):c.346C>A (p.Arg116Ser)	not specified [RCV005328144]	uncertain significance	9	98808044	98808044	Human		name
598202790	CV3977620	single nucleotide variant	NM_024642.5(GALNT12):c.922C>G (p.Pro308Ala)	not specified [RCV005337157]	uncertain significance	9	98835253	98835253	Human		name
598202796	CV3977621	single nucleotide variant	NM_024642.5(GALNT12):c.483G>C (p.Glu161Asp)	not specified [RCV005337158]	uncertain significance	9	98823367	98823367	Human		name
598202816	CV3977624	single nucleotide variant	NM_024642.5(GALNT12):c.568G>C (p.Glu190Gln)	not specified [RCV005337161]	uncertain significance	9	98826778	98826778	Human		name
598202836	CV3977627	single nucleotide variant	NM_024642.5(GALNT12):c.443C>A (p.Ala148Asp)	not specified [RCV005337164]	uncertain significance	9	98823327	98823327	Human		name
598158845	CV3977628	single nucleotide variant	NM_024642.5(GALNT12):c.305A>G (p.Gln102Arg)	not specified [RCV005328145]	uncertain significance	9	98808003	98808003	Human		name
598202842	CV3977629	single nucleotide variant	NM_024642.5(GALNT12):c.533G>A (p.Ser178Asn)	not specified [RCV005337165]	uncertain significance	9	98823417	98823417	Human		name
598202847	CV3977630	single nucleotide variant	NM_024642.5(GALNT12):c.819G>T (p.Glu273Asp)	not specified [RCV005337166]	uncertain significance	9	98831859	98831859	Human		name
598158850	CV3977634	single nucleotide variant	NM_024642.5(GALNT12):c.433T>C (p.Tyr145His)	not specified [RCV005328146]	uncertain significance	9	98823317	98823317	Human		name
598190270	CV4008813	single nucleotide variant	NM_024642.5(GALNT12):c.422T>C (p.Ile141Thr)	Colorectal cancer, susceptibility to, 1 [RCV005396312]	uncertain significance	9	98823306	98823306	Human	1	name
598190914	CV4008894	single nucleotide variant	NM_024642.5(GALNT12):c.931G>T (p.Ala311Ser)	Colorectal cancer, susceptibility to, 1 [RCV005396395]	uncertain significance	9	98835262	98835262	Human	1	name
8625159	CV80278	single nucleotide variant	NM_052917.3(GALNT13):c.937G>A (p.Asp313Asn)	Malignant melanoma [RCV000060354]	not provided	2	154259100	154259100	Human		name
8629894	CV85041	single nucleotide variant	NM_052917.3(GALNT13):c.689A>T (p.Lys230Ile)	Malignant melanoma [RCV000065123]	not provided	2	154245814	154245814	Human		name
8633149	CV88362	single nucleotide variant	NM_024642.5(GALNT12):c.985G>A (p.Asp329Asn)	Colorectal cancer, susceptibility to, 1 [RCV004572398]\|not provided [RCV003094884]\|not specified [RCV004057659]	uncertain significance\|not provided	9	98835316	98835316	Human	1	name

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