Zbtb16 Variant Search Result - Rat Genome Database

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81 records found for search term Zbtb16

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15141471	CV759992	single nucleotide variant	NM_006006.6(ZBTB16):c.1624+7C>G	not provided [RCV000921846]	likely benign	11	114242344	114242344	Human		name
401909740	CV2809866	single nucleotide variant	NM_006006.6(ZBTB16):c.1269-3228A>G	not provided [RCV003398139]	likely benign	11	114153109	114153109	Human		name
8652550	CV129125	single nucleotide variant	NM_006006.4(ZBTB16):c.1268+11773T>C	Lung cancer [RCV000109612]	uncertain significance	11	114076341	114076341	Human		name
401934061	CV2809864	single nucleotide variant	NM_006006.6(ZBTB16):c.90C>T (p.Ala30=)	not provided [RCV003410920]	likely benign	11	114063390	114063390	Human		name
405285110	CV3202406	single nucleotide variant	NM_006006.6(ZBTB16):c.31C>T (p.Leu11=)	ZBTB16-related disorder [RCV003909675]	likely benign	11	114063331	114063331	Human		name , trait , alternate_id
405285325	CV3212362	single nucleotide variant	NM_006006.6(ZBTB16):c.207C>T (p.His69=)	ZBTB16-related disorder [RCV003958974]	likely benign	11	114063507	114063507	Human		name , trait , alternate_id
15202159	CV768209	single nucleotide variant	NM_006006.6(ZBTB16):c.261A>G (p.Ala87=)	not provided [RCV000935866]	likely benign	11	114063561	114063561	Human		name
401909738	CV2809865	single nucleotide variant	NM_006006.6(ZBTB16):c.414C>T (p.Ala138=)	not provided [RCV003398138]	likely benign	11	114063714	114063714	Human		name
15199310	CV701567	single nucleotide variant	NM_006006.6(ZBTB16):c.399G>A (p.Thr133=)	not provided [RCV000957004]	benign	11	114063699	114063699	Human		name
15174982	CV737733	single nucleotide variant	NM_006006.6(ZBTB16):c.672C>G (p.Pro224=)	not provided [RCV000906103]	benign\|likely benign	11	114063972	114063972	Human		name
15144388	CV737734	single nucleotide variant	NM_006006.6(ZBTB16):c.672C>T (p.Pro224=)	not provided [RCV000899996]	benign	11	114063972	114063972	Human		name
15177399	CV737735	single nucleotide variant	NM_006006.6(ZBTB16):c.813G>A (p.Lys271=)	not provided [RCV000906642]	likely benign	11	114064113	114064113	Human		name
15135213	CV737736	single nucleotide variant	NM_006006.6(ZBTB16):c.939C>T (p.Gly313=)	not provided [RCV000898417]	likely benign	11	114064239	114064239	Human		name
15164437	CV752430	single nucleotide variant	NM_006006.6(ZBTB16):c.426C>T (p.Ala142=)	not provided [RCV000926381]	benign\|likely benign	11	114063726	114063726	Human		name
15108289	CV752431	single nucleotide variant	NM_006006.6(ZBTB16):c.756C>T (p.Pro252=)	not provided [RCV000916114]	likely benign	11	114064056	114064056	Human		name
15136763	CV752432	single nucleotide variant	NM_006006.6(ZBTB16):c.780C>T (p.Ala260=)	not provided [RCV000921061]	likely benign	11	114064080	114064080	Human		name
15195329	CV768210	single nucleotide variant	NM_006006.6(ZBTB16):c.402G>A (p.Glu134=)	not provided [RCV000933906]	likely benign	11	114063702	114063702	Human		name
8652549	CV129124	single nucleotide variant	NM_006006.4(ZBTB16):c.1200G>T (p.Arg400=)	Lung cancer [RCV000109611]	uncertain significance	11	114064500	114064500	Human		name
151353145	CV1326059	single nucleotide variant	NM_006006.6(ZBTB16):c.1998G>A (p.Thr666=)	not provided [RCV001816109]	likely benign	11	114250531	114250531	Human		name
401909743	CV2809867	single nucleotide variant	NM_006006.6(ZBTB16):c.1626C>T (p.Gly542=)	not provided [RCV003398140]	likely benign	11	114247199	114247199	Human		name
405291730	CV3206069	single nucleotide variant	NM_006006.6(ZBTB16):c.1398C>T (p.Cys466=)	ZBTB16-related disorder [RCV003964152]	likely benign	11	114186983	114186983	Human		name , trait , alternate_id
405271342	CV3209311	single nucleotide variant	NM_006006.6(ZBTB16):c.1029C>T (p.Asp343=)	ZBTB16-related disorder [RCV003949659]	likely benign	11	114064329	114064329	Human		name , trait , alternate_id
405266784	CV3211926	single nucleotide variant	NM_006006.6(ZBTB16):c.2004C>T (p.Leu668=)	ZBTB16-related disorder [RCV003947195]	likely benign	11	114250537	114250537	Human		name , trait , alternate_id
596948064	CV3547656	single nucleotide variant	NM_006006.6(ZBTB16):c.1995G>A (p.Lys665=)	not provided [RCV004811961]	likely benign	11	114250528	114250528	Human		name
597752563	CV3627663	single nucleotide variant	NM_006006.6(ZBTB16):c.190C>A (p.His64Asn)	not specified [RCV004892995]	uncertain significance	11	114063490	114063490	Human		name
598243038	CV3930307	single nucleotide variant	NM_006006.6(ZBTB16):c.283A>C (p.Lys95Gln)	not specified [RCV005297217]	uncertain significance	11	114063583	114063583	Human		name
15185400	CV701568	single nucleotide variant	NM_006006.6(ZBTB16):c.1542C>T (p.Gly514=)	not provided [RCV000952970]	likely benign	11	114242255	114242255	Human		name
15197282	CV724198	single nucleotide variant	NM_006006.6(ZBTB16):c.1248C>T (p.Asn416=)	not provided [RCV000890014]	benign	11	114064548	114064548	Human		name
15177212	CV737737	single nucleotide variant	NM_006006.6(ZBTB16):c.1005C>T (p.Ser335=)	not provided [RCV000906600]	benign	11	114064305	114064305	Human		name
15173235	CV737738	single nucleotide variant	NM_006006.6(ZBTB16):c.1293G>A (p.Thr431=)	not provided [RCV000905823]	likely benign	11	114156361	114156361	Human		name
15201231	CV752433	single nucleotide variant	NM_006006.6(ZBTB16):c.1047G>A (p.Pro349=)	not provided [RCV000913078]	likely benign	11	114064347	114064347	Human		name
15126612	CV752434	single nucleotide variant	NM_006006.6(ZBTB16):c.1176T>C (p.Ala392=)	not provided [RCV000919355]	likely benign	11	114064476	114064476	Human		name
152999716	CV1683283	single nucleotide variant	NM_006006.6(ZBTB16):c.443G>A (p.Arg148His)	See cases [RCV002252467]\|not specified [RCV004047389]	uncertain significance	11	114063743	114063743	Human		name
156307751	CV2249424	single nucleotide variant	NM_006006.6(ZBTB16):c.704A>G (p.His235Arg)	not specified [RCV004120483]	uncertain significance	11	114064004	114064004	Human		name
155957990	CV2304230	single nucleotide variant	NM_006006.6(ZBTB16):c.457C>G (p.Leu153Val)	not specified [RCV004170249]	uncertain significance	11	114063757	114063757	Human		name
155956163	CV2387228	single nucleotide variant	NM_006006.6(ZBTB16):c.590G>A (p.Ser197Asn)	not specified [RCV004238325]	uncertain significance	11	114063890	114063890	Human		name
156220179	CV2393692	single nucleotide variant	NM_006006.6(ZBTB16):c.728C>T (p.Thr243Met)	not specified [RCV004231496]	uncertain significance	11	114064028	114064028	Human		name
329359449	CV2446269	single nucleotide variant	NM_006006.6(ZBTB16):c.772G>A (p.Gly258Arg)	not specified [RCV004249405]	uncertain significance	11	114064072	114064072	Human		name
401756301	CV2687079	single nucleotide variant	NM_006006.6(ZBTB16):c.977C>T (p.Pro326Leu)	not specified [RCV004304397]	uncertain significance	11	114064277	114064277	Human		name
405271219	CV3218998	single nucleotide variant	NM_006006.6(ZBTB16):c.565A>G (p.Thr189Ala)	ZBTB16-related disorder [RCV003971725]	likely benign	11	114063865	114063865	Human		name , trait , alternate_id
405803367	CV3356778	single nucleotide variant	NM_006006.6(ZBTB16):c.442C>T (p.Arg148Cys)	not specified [RCV004478780]	uncertain significance	11	114063742	114063742	Human		name
405803369	CV3356779	single nucleotide variant	NM_006006.6(ZBTB16):c.529C>T (p.Pro177Ser)	not specified [RCV004478781]	uncertain significance	11	114063829	114063829	Human		name
405803371	CV3356780	single nucleotide variant	NM_006006.6(ZBTB16):c.678G>C (p.Glu226Asp)	not specified [RCV004478782]	uncertain significance	11	114063978	114063978	Human		name
405803373	CV3356781	single nucleotide variant	NM_006006.6(ZBTB16):c.700C>T (p.Arg234Trp)	not specified [RCV004478783]	uncertain significance	11	114064000	114064000	Human		name
405803377	CV3356783	single nucleotide variant	NM_006006.6(ZBTB16):c.757A>G (p.Ser253Gly)	not specified [RCV004478785]	likely benign	11	114064057	114064057	Human		name
405803379	CV3356784	single nucleotide variant	NM_006006.6(ZBTB16):c.923C>A (p.Pro308His)	not specified [RCV004478786]	uncertain significance	11	114064223	114064223	Human		name
407529789	CV3493990	single nucleotide variant	NM_006006.6(ZBTB16):c.683C>T (p.Thr228Ile)	not specified [RCV004681096]	uncertain significance	11	114063983	114063983	Human		name
407529791	CV3493991	single nucleotide variant	NM_006006.6(ZBTB16):c.490G>C (p.Glu164Gln)	not specified [RCV004681097]	uncertain significance	11	114063790	114063790	Human		name
597692501	CV3627655	single nucleotide variant	NM_006006.6(ZBTB16):c.629G>A (p.Gly210Glu)	not specified [RCV004884767]	uncertain significance	11	114063929	114063929	Human		name
597752549	CV3627657	single nucleotide variant	NM_006006.6(ZBTB16):c.910G>A (p.Glu304Lys)	not specified [RCV004892992]	uncertain significance	11	114064210	114064210	Human		name
597692532	CV3627659	single nucleotide variant	NM_006006.6(ZBTB16):c.896G>C (p.Arg299Pro)	not specified [RCV004884770]	uncertain significance	11	114064196	114064196	Human		name
597752558	CV3627661	single nucleotide variant	NM_006006.6(ZBTB16):c.838C>T (p.Pro280Ser)	not specified [RCV004892994]	uncertain significance	11	114064138	114064138	Human		name
597692542	CV3627662	single nucleotide variant	NM_006006.6(ZBTB16):c.451C>T (p.Arg151Trp)	not specified [RCV004884771]	uncertain significance	11	114063751	114063751	Human		name
597752566	CV3627666	single nucleotide variant	NM_006006.6(ZBTB16):c.497G>T (p.Ser166Ile)	not specified [RCV004892996]	uncertain significance	11	114063797	114063797	Human		name
598196473	CV3930304	single nucleotide variant	NM_006006.6(ZBTB16):c.622A>C (p.Thr208Pro)	not specified [RCV005313522]	uncertain significance	11	114063922	114063922	Human		name
156123992	CV2234156	single nucleotide variant	NM_006006.6(ZBTB16):c.1303G>A (p.Glu435Lys)	not specified [RCV004106245]	uncertain significance	11	114156371	114156371	Human		name
156081127	CV2256035	single nucleotide variant	NM_006006.6(ZBTB16):c.1084C>A (p.Leu362Met)	not specified [RCV004122468]	uncertain significance	11	114064384	114064384	Human		name
156391754	CV2382545	single nucleotide variant	NM_006006.6(ZBTB16):c.1222G>A (p.Val408Met)	not specified [RCV004232875]	uncertain significance	11	114064522	114064522	Human		name
156048183	CV2390992	single nucleotide variant	NM_006006.6(ZBTB16):c.1006G>A (p.Val336Met)	not specified [RCV004234992]	uncertain significance	11	114064306	114064306	Human		name
401770757	CV2707393	single nucleotide variant	NM_006006.6(ZBTB16):c.1229G>A (p.Gly410Glu)	not specified [RCV004312781]	uncertain significance	11	114064529	114064529	Human		name
401738246	CV2714377	single nucleotide variant	NM_006006.6(ZBTB16):c.1030G>A (p.Ala344Thr)	not specified [RCV004317912]	uncertain significance	11	114064330	114064330	Human		name
401884100	CV2765036	single nucleotide variant	NM_006006.6(ZBTB16):c.1183A>G (p.Met395Val)	not specified [RCV004337157]	uncertain significance	11	114064483	114064483	Human		name
8563659	CV28415	single nucleotide variant	NM_006006.6(ZBTB16):c.1849A>G (p.Met617Val)	Skeletal defects, genital hypoplasia, and intellectual disability [RCV000014305]	pathogenic\|uncertain significance	11	114250382	114250382	Human	1	name
405803354	CV3356772	single nucleotide variant	NM_006006.6(ZBTB16):c.1204A>G (p.Ile402Val)	not specified [RCV004478774]	uncertain significance	11	114064504	114064504	Human		name
405803356	CV3356773	single nucleotide variant	NM_006006.6(ZBTB16):c.1204A>T (p.Ile402Phe)	not specified [RCV004478775]	uncertain significance	11	114064504	114064504	Human		name
405803358	CV3356774	single nucleotide variant	NM_006006.6(ZBTB16):c.1463T>C (p.Met488Thr)	not specified [RCV004478776]	uncertain significance	11	114242176	114242176	Human		name
405803360	CV3356775	single nucleotide variant	NM_006006.6(ZBTB16):c.1481T>C (p.Leu494Pro)	not specified [RCV004478777]	uncertain significance	11	114242194	114242194	Human		name
405803362	CV3356776	single nucleotide variant	NM_006006.6(ZBTB16):c.1493G>A (p.Arg498His)	not specified [RCV004478778]	uncertain significance	11	114242206	114242206	Human		name
405803364	CV3356777	single nucleotide variant	NM_006006.6(ZBTB16):c.1699A>C (p.Ile567Leu)	not specified [RCV004478779]	uncertain significance	11	114247272	114247272	Human		name
597692509	CV3627656	single nucleotide variant	NM_006006.6(ZBTB16):c.1538C>T (p.Ala513Val)	not specified [RCV004884768]	uncertain significance	11	114242251	114242251	Human		name
597692520	CV3627658	single nucleotide variant	NM_006006.6(ZBTB16):c.1385T>C (p.Val462Ala)	not specified [RCV004884769]	uncertain significance	11	114186970	114186970	Human		name
597692554	CV3627664	single nucleotide variant	NM_006006.6(ZBTB16):c.1076A>C (p.Gln359Pro)	not specified [RCV004884772]	uncertain significance	11	114064376	114064376	Human		name
597692566	CV3627665	single nucleotide variant	NM_006006.6(ZBTB16):c.1197C>A (p.Ser399Arg)	not specified [RCV004884773]	uncertain significance	11	114064497	114064497	Human		name
598243021	CV3930302	single nucleotide variant	NM_006006.6(ZBTB16):c.1627G>A (p.Asp543Asn)	not specified [RCV005297214]	uncertain significance	11	114247200	114247200	Human		name
598243028	CV3930303	single nucleotide variant	NM_006006.6(ZBTB16):c.1292C>T (p.Thr431Met)	not specified [RCV005297215]	uncertain significance	11	114156360	114156360	Human		name
598243032	CV3930305	single nucleotide variant	NM_006006.6(ZBTB16):c.1265A>C (p.His422Pro)	not specified [RCV005297216]	uncertain significance	11	114064565	114064565	Human		name
598196479	CV3930306	single nucleotide variant	NM_006006.6(ZBTB16):c.1145G>A (p.Arg382Lys)	not specified [RCV005313523]	uncertain significance	11	114064445	114064445	Human		name
598243044	CV3930308	single nucleotide variant	NM_006006.6(ZBTB16):c.1073T>A (p.Val358Glu)	not specified [RCV005297218]	uncertain significance	11	114064373	114064373	Human		name
15141959	CV712610	single nucleotide variant	NM_006006.6(ZBTB16):c.1072G>A (p.Val358Met)	ZBTB16-related disorder [RCV003905910]\|not provided [RCV000966396]	likely benign	11	114064372	114064372	Human	1	name , trait , alternate_id
21074121	CV796519	single nucleotide variant	NM_006006.6(ZBTB16):c.1883C>T (p.Ser628Leu)	not provided [RCV000994728]	uncertain significance	11	114250416	114250416	Human		name
8626905	CV82049	single nucleotide variant	NM_006006.4(ZBTB16):c.1528G>A (p.Glu510Lys)	Malignant melanoma [RCV000062128]	not provided	11	114242241	114242241	Human		name

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