Cdk10 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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130 records found for search term Cdk10

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
126741448	CV1021576	single nucleotide variant	NM_052988.5(CDK10):c.*36G>A	Al Kaissi syndrome [RCV001336258]	pathogenic	16	89695728	89695728	Human		name
405265220	CV3190396	single nucleotide variant	NM_052988.5(CDK10):c.*90G>A	CDK10-related disorder [RCV003897246]	likely benign	16	89695782	89695782	Human		name , trait , alternate_id
405288264	CV3211262	single nucleotide variant	NM_052988.5(CDK10):c.*82G>A	CDK10-related disorder [RCV003924765]	likely benign	16	89695774	89695774	Human		name , trait , alternate_id
401830013	CV2747732	single nucleotide variant	NM_052988.5(CDK10):c.87+5G>A	Al Kaissi syndrome [RCV003329150]\|not provided [RCV005003056]	pathogenic\|likely pathogenic	16	89686802	89686802	Human	1	name
401830052	CV2747734	single nucleotide variant	NM_052988.5(CDK10):c.161-1G>C	Al Kaissi syndrome [RCV003329152]	pathogenic	16	89690552	89690552	Human	1	name
405285846	CV3191927	single nucleotide variant	NM_052988.5(CDK10):c.792+7G>A	CDK10-related disorder [RCV003923869]	likely benign	16	89694795	89694795	Human		name , trait , alternate_id
405286634	CV3192867	single nucleotide variant	NM_052988.5(CDK10):c.417+5G>A	CDK10-related disorder [RCV003981585]	likely benign	16	89691892	89691892	Human		name , trait , alternate_id
405258485	CV3203853	single nucleotide variant	NM_052988.5(CDK10):c.609-7T>G	CDK10-related disorder [RCV003942020]	likely benign	16	89694166	89694166	Human		name , trait , alternate_id
405270909	CV3218825	single nucleotide variant	NM_052988.5(CDK10):c.485+7G>C	CDK10-related disorder [RCV003971583]	likely benign	16	89692523	89692523	Human		name , trait , alternate_id
597655562	CV3642085	single nucleotide variant	NM_052988.5(CDK10):c.793-3T>C	Inborn genetic diseases [RCV004976245]	uncertain significance	16	89694928	89694928	Human	1	name
597655543	CV3642088	single nucleotide variant	NM_052988.5(CDK10):c.609-4G>T	Inborn genetic diseases [RCV004976248]\|not provided [RCV005244094]	likely benign\|uncertain significance	16	89694169	89694169	Human	1	name
598129796	CV3887217	single nucleotide variant	NM_052988.5(CDK10):c.233-8C>T	not provided [RCV005245277]	uncertain significance	16	89691435	89691435	Human		name
13437604	CV434381	single nucleotide variant	NM_052988.5(CDK10):c.609-1G>A	Al Kaissi syndrome [RCV000508995]\|not provided [RCV003313089]	pathogenic\|likely pathogenic	16	89694172	89694172	Human	1	name
13437603	CV434384	single nucleotide variant	NM_052988.5(CDK10):c.608+1G>A	Al Kaissi syndrome [RCV000508994]\|not provided [RCV001091059]	pathogenic	16	89693468	89693468	Human	1	name
150408757	CV1182678	single nucleotide variant	NM_052988.5(CDK10):c.485+49A>G	Al Kaissi syndrome [RCV001554873]\|not provided [RCV004710322]	benign	16	89692565	89692565	Human	1	name
150408761	CV1182679	single nucleotide variant	NM_052988.5(CDK10):c.609-29T>C	Al Kaissi syndrome [RCV001554874]\|not provided [RCV004710323]	benign	16	89694144	89694144	Human	1	name
8635952	CV91175	single nucleotide variant	NM_001098533.2(CDK10):c.325+24C>T	Malignant melanoma [RCV000071273]	not provided	16	89693350	89693350	Human		name
401725616	CV2735915	single nucleotide variant	NM_052988.5(CDK10):c.12A>T (p.Pro4=)	not provided [RCV003312359]	likely benign	16	89686722	89686722	Human		name
126736841	CV1018206	single nucleotide variant	NM_052988.5(CDK10):c.51T>G (p.Arg17=)	Al Kaissi syndrome [RCV001328627]\|not provided [RCV003426045]	likely benign\|uncertain significance	16	89686761	89686761	Human	1	name
401903618	CV2814606	deletion	NM_052988.5(CDK10):c.608+10_608+12del	not provided [RCV003419533]	likely benign	16	89693475	89693477	Human		name
407455216	CV3422417	single nucleotide variant	NM_052988.5(CDK10):c.5C>T (p.Ala2Val)	Inborn genetic diseases [RCV004610208]	uncertain significance	16	89686715	89686715	Human	1	name
597655571	CV3642083	single nucleotide variant	NM_052988.5(CDK10):c.4G>A (p.Ala2Thr)	Inborn genetic diseases [RCV004976243]	uncertain significance	16	89686714	89686714	Human	1	name
401725611	CV2735914	single nucleotide variant	NM_052988.5(CDK10):c.10C>G (p.Pro4Ala)	not provided [RCV003312358]	likely benign	16	89686720	89686720	Human	1	name
401725611	CV2735914	single nucleotide variant	NM_052988.5(CDK10):c.10C>G (p.Pro4Ala)	not provided [RCV003312358]	likely benign	16	89686720	89686721	Human	1	name
401830011	CV2747731	single nucleotide variant	NM_052988.5(CDK10):c.25G>C (p.Glu9Gln)	Al Kaissi syndrome [RCV003329149]\|Inborn genetic diseases [RCV004334101]	uncertain significance	16	89686735	89686735	Human	2	name
13437609	CV434382	deletion	NM_052988.5(CDK10):c.88-870_232+368del	Al Kaissi syndrome [RCV000509000]	pathogenic	16	89688382	89690992	Human	1	name
41408277	CV980808	single nucleotide variant	NM_052988.5(CDK10):c.24C>A (p.Cys8Ter)	Al Kaissi syndrome [RCV003329120]\|not provided [RCV001281658]	pathogenic\|likely pathogenic	16	89686734	89686734	Human	1	name
156258412	CV2219979	single nucleotide variant	NM_052988.5(CDK10):c.86G>A (p.Arg29Lys)	Inborn genetic diseases [RCV002702873]	uncertain significance	16	89686796	89686796	Human	1	name
156123087	CV2233942	single nucleotide variant	NM_052988.5(CDK10):c.41A>G (p.Lys14Arg)	Inborn genetic diseases [RCV002762431]	uncertain significance	16	89686751	89686751	Human	1	name
156359146	CV2261013	single nucleotide variant	NM_052988.5(CDK10):c.98G>A (p.Cys33Tyr)	Inborn genetic diseases [RCV002812549]	uncertain significance	16	89689262	89689262	Human	1	name
156246657	CV2276778	single nucleotide variant	NM_052988.5(CDK10):c.37C>A (p.Leu13Met)	Inborn genetic diseases [RCV002854579]	uncertain significance	16	89686747	89686747	Human	1	name
401725622	CV2735916	single nucleotide variant	NM_052988.5(CDK10):c.645G>A (p.Thr215=)	not provided [RCV003312360]	likely benign	16	89694209	89694209	Human		name
401830010	CV2747730	single nucleotide variant	NM_052988.5(CDK10):c.792G>A (p.Pro264=)	Al Kaissi syndrome [RCV003329148]	pathogenic	16	89694788	89694788	Human	1	name
401903617	CV2814604	single nucleotide variant	NM_052988.5(CDK10):c.429C>T (p.Ile143=)	not provided [RCV003419532]	likely benign	16	89692460	89692460	Human		name
401935603	CV2814605	single nucleotide variant	NM_052988.5(CDK10):c.570C>T (p.Val190=)	not provided [RCV003413060]	likely benign	16	89693429	89693429	Human		name
401903621	CV2814607	single nucleotide variant	NM_052988.5(CDK10):c.936G>A (p.Ala312=)	not provided [RCV003419534]	likely benign	16	89695296	89695296	Human		name
401903622	CV2814608	single nucleotide variant	NM_052988.5(CDK10):c.942C>T (p.Ala314=)	CDK10-related disorder [RCV003938943]\|not provided [RCV003419535]	likely benign	16	89695302	89695302	Human	1	name , trait , alternate_id
405267622	CV3186874	single nucleotide variant	NM_052988.5(CDK10):c.717C>A (p.Leu239=)	not provided [RCV003886957]	likely benign	16	89694713	89694713	Human		name
405290089	CV3205972	single nucleotide variant	NM_052988.5(CDK10):c.546C>T (p.Phe182=)	CDK10-related disorder [RCV003962125]	likely benign	16	89693405	89693405	Human		name , trait , alternate_id
405266278	CV3215908	single nucleotide variant	NM_052988.5(CDK10):c.474C>T (p.Phe158=)	CDK10-related disorder [RCV003947041]	likely benign	16	89692505	89692505	Human		name , trait , alternate_id
407453590	CV3416355	single nucleotide variant	NM_052988.5(CDK10):c.822G>A (p.Gln274=)	not provided [RCV004597613]	benign	16	89694960	89694960	Human		name
13437611	CV434383	deletion	NM_052988.5(CDK10):c.139del (p.Glu47fs)	Al Kaissi syndrome [RCV000509002]	pathogenic\|likely pathogenic	16	89689303	89689303	Human	1	name
40887720	CV974030	deletion	NM_052988.5(CDK10):c.178del (p.Gln60fs)	Inborn genetic diseases [RCV001267315]	pathogenic	16	89690568	89690568	Human	1	name
126725750	CV1018207	single nucleotide variant	NM_052988.5(CDK10):c.169C>T (p.Arg57Trp)	Al Kaissi syndrome [RCV001331580]\|Inborn genetic diseases [RCV002546493]\|not provided [RCV001532330]	uncertain significance	16	89690561	89690561	Human	2	name
126736856	CV1018208	single nucleotide variant	NM_052988.5(CDK10):c.263C>G (p.Thr88Arg)	Al Kaissi syndrome [RCV001328630]	uncertain significance	16	89691473	89691473	Human	1	name
126741457	CV1021574	single nucleotide variant	NM_052988.5(CDK10):c.295G>C (p.Val99Leu)	Al Kaissi syndrome [RCV001336260]	uncertain significance	16	89691505	89691505	Human	1	name
151349387	CV1170323	single nucleotide variant	NM_052988.5(CDK10):c.202A>T (p.Lys68Ter)	not provided [RCV001814581]	likely pathogenic	16	89690594	89690594	Human		name
150536834	CV1314315	deletion	NM_052988.5(CDK10):c.794del (p.Gly265fs)	Al Kaissi syndrome [RCV001780741]	likely pathogenic	16	89694930	89694930	Human		name
155973086	CV2238908	single nucleotide variant	NM_052988.5(CDK10):c.208G>A (p.Val70Met)	Inborn genetic diseases [RCV002777018]	uncertain significance	16	89690600	89690600	Human	1	name
156222217	CV2394611	single nucleotide variant	NM_052988.5(CDK10):c.101G>A (p.Arg34Gln)	Inborn genetic diseases [RCV002744808]	uncertain significance	16	89689265	89689265	Human	1	name
401830014	CV2747735	single nucleotide variant	NM_052988.5(CDK10):c.226A>T (p.Lys76Ter)	Al Kaissi syndrome [RCV003329153]	pathogenic	16	89690618	89690618	Human	1	name
401830020	CV2747738	deletion	NM_052988.5(CDK10):c.503del (p.Asn168fs)	Al Kaissi syndrome [RCV003329156]	pathogenic	16	89693290	89693290	Human	1	name
401896596	CV2791705	single nucleotide variant	NM_052988.5(CDK10):c.295G>A (p.Val99Met)	Inborn genetic diseases [RCV003374232]	uncertain significance	16	89691505	89691505	Human	1	name
405266749	CV3211896	single nucleotide variant	NM_052988.5(CDK10):c.1082G>A (p.Ter361=)	CDK10-related disorder [RCV003947171]	likely benign	16	89695691	89695691	Human		name , trait , alternate_id
405722262	CV3292857	single nucleotide variant	NM_052988.5(CDK10):c.170G>A (p.Arg57Gln)	Inborn genetic diseases [RCV004428298]	uncertain significance	16	89690562	89690562	Human	1	name
407455212	CV3422415	single nucleotide variant	NM_052988.5(CDK10):c.230A>G (p.Asp77Gly)	Inborn genetic diseases [RCV004610206]	uncertain significance	16	89690622	89690622	Human	1	name
597655578	CV3642082	single nucleotide variant	NM_052988.5(CDK10):c.130C>T (p.Arg44Cys)	Inborn genetic diseases [RCV004976242]	uncertain significance	16	89689294	89689294	Human	1	name
597655566	CV3642084	single nucleotide variant	NM_052988.5(CDK10):c.280C>T (p.Arg94Cys)	Inborn genetic diseases [RCV004976244]	uncertain significance	16	89691490	89691490	Human	1	name
597655530	CV3642090	single nucleotide variant	NM_052988.5(CDK10):c.191T>C (p.Ile64Thr)	Inborn genetic diseases [RCV004976250]	uncertain significance	16	89690583	89690583	Human	1	name
598222543	CV3892296	single nucleotide variant	NM_052988.5(CDK10):c.202A>G (p.Lys68Glu)	Al Kaissi syndrome [RCV005253635]	uncertain significance	16	89690594	89690594	Human	1	name
598229832	CV3943619	single nucleotide variant	NM_052988.5(CDK10):c.211C>T (p.Arg71Trp)	Inborn genetic diseases [RCV005319294]	uncertain significance	16	89690603	89690603	Human	1	name
616938230	CV4013099	single nucleotide variant	NM_052988.5(CDK10):c.239C>T (p.Pro80Leu)	not provided [RCV005410566]	uncertain significance	16	89691449	89691449	Human		name
40889687	CV975455	deletion	NM_052988.5(CDK10):c.729del (p.Glu244fs)	Al Kaissi syndrome [RCV001729831]\|not provided [RCV001268115]	likely pathogenic	16	89694724	89694724	Human	1	name
126736846	CV1018209	single nucleotide variant	NM_052988.5(CDK10):c.527G>C (p.Cys176Ser)	Al Kaissi syndrome [RCV001328628]\|Inborn genetic diseases [RCV003346475]	uncertain significance	16	89693315	89693315	Human	2	name
126736851	CV1018210	single nucleotide variant	NM_052988.5(CDK10):c.661G>A (p.Asp221Asn)	Al Kaissi syndrome [RCV001328629]\|not provided [RCV004770058]	uncertain significance	16	89694225	89694225	Human	1	name
126741453	CV1021575	single nucleotide variant	NM_052988.5(CDK10):c.684A>G (p.Ile228Met)	Al Kaissi syndrome [RCV001336259]	uncertain significance	16	89694680	89694680	Human	1	name
150337031	CV1166213	single nucleotide variant	NM_052988.5(CDK10):c.685C>G (p.Leu229Val)	Inborn genetic diseases [RCV003246978]\|not provided [RCV001532332]	uncertain significance	16	89694681	89694681	Human	1	name
150549556	CV1295314	single nucleotide variant	NM_052988.5(CDK10):c.614G>A (p.Arg205Gln)	not provided [RCV001765214]	uncertain significance	16	89694178	89694178	Human		name
155265521	CV1704880	single nucleotide variant	NM_052988.5(CDK10):c.872G>A (p.Trp291Ter)	Global developmental delay [RCV002285125]	pathogenic	16	89695010	89695010	Human	2	name
155987007	CV2234051	single nucleotide variant	NM_052988.5(CDK10):c.514A>G (p.Thr172Ala)	Inborn genetic diseases [RCV002732970]	uncertain significance	16	89693302	89693302	Human	1	name
156149485	CV2265355	single nucleotide variant	NM_052988.5(CDK10):c.707G>A (p.Arg236Lys)	Inborn genetic diseases [RCV002826696]	likely benign	16	89694703	89694703	Human	1	name
155954875	CV2302278	single nucleotide variant	NM_052988.5(CDK10):c.944G>A (p.Gly315Glu)	Inborn genetic diseases [RCV002905457]	uncertain significance	16	89695304	89695304	Human	1	name
156161521	CV2311745	single nucleotide variant	NM_052988.5(CDK10):c.442C>T (p.Leu148Phe)	Inborn genetic diseases [RCV002916015]	uncertain significance	16	89692473	89692473	Human	1	name
156339015	CV2351515	single nucleotide variant	NM_052988.5(CDK10):c.407C>T (p.Ser136Leu)	Inborn genetic diseases [RCV002965072]	uncertain significance	16	89691877	89691877	Human	1	name
156056033	CV2370993	single nucleotide variant	NM_052988.5(CDK10):c.583A>G (p.Met195Val)	Inborn genetic diseases [RCV002693132]\|not provided [RCV005001358]	uncertain significance	16	89693442	89693442	Human	1	name
155970420	CV2392222	single nucleotide variant	NM_052988.5(CDK10):c.882G>T (p.Glu294Asp)	Inborn genetic diseases [RCV002754833]	uncertain significance	16	89695020	89695020	Human	1	name
243055010	CV2407216	single nucleotide variant	NM_052988.5(CDK10):c.886G>A (p.Gly296Arg)	Al Kaissi syndrome [RCV003144766]	uncertain significance	16	89695024	89695024	Human	1	name
243055012	CV2407217	single nucleotide variant	NM_052988.5(CDK10):c.638C>T (p.Thr213Ile)	Al Kaissi syndrome [RCV003144767]	uncertain significance	16	89694202	89694202	Human	1	name
329400287	CV2437575	single nucleotide variant	NM_052988.5(CDK10):c.938C>T (p.Thr313Met)	Inborn genetic diseases [RCV003197276]	uncertain significance	16	89695298	89695298	Human	1	name
329360994	CV2439766	single nucleotide variant	NM_052988.5(CDK10):c.556C>T (p.Arg186Trp)	Inborn genetic diseases [RCV003180096]	uncertain significance	16	89693415	89693415	Human	1	name
329349962	CV2450881	single nucleotide variant	NM_052988.5(CDK10):c.313G>A (p.Val105Ile)	Inborn genetic diseases [RCV003204351]\|not provided [RCV003222489]	uncertain significance	16	89691523	89691523	Human	1	name
401724532	CV2677909	single nucleotide variant	NM_052988.5(CDK10):c.546C>G (p.Phe182Leu)	Inborn genetic diseases [RCV003245496]	uncertain significance	16	89693405	89693405	Human	1	name
401782228	CV2686602	single nucleotide variant	NM_052988.5(CDK10):c.805C>G (p.Leu269Val)	Inborn genetic diseases [RCV003265635]\|not provided [RCV004779525]	uncertain significance	16	89694943	89694943	Human	1	name
401830017	CV2747736	single nucleotide variant	NM_052988.5(CDK10):c.452T>C (p.Leu151Pro)	Al Kaissi syndrome [RCV003329154]	pathogenic	16	89692483	89692483	Human	1	name
401830018	CV2747737	single nucleotide variant	NM_052988.5(CDK10):c.461T>C (p.Leu154Pro)	Al Kaissi syndrome [RCV003329155]	pathogenic	16	89692492	89692492	Human	1	name
405722278	CV3292859	single nucleotide variant	NM_052988.5(CDK10):c.635G>A (p.Gly212Glu)	Inborn genetic diseases [RCV004428300]	uncertain significance	16	89694199	89694199	Human	1	name
405722286	CV3292860	single nucleotide variant	NM_052988.5(CDK10):c.658A>G (p.Ile220Val)	Inborn genetic diseases [RCV004428301]	uncertain significance	16	89694222	89694222	Human	1	name
405722296	CV3292861	single nucleotide variant	NM_052988.5(CDK10):c.833G>A (p.Arg278Gln)	Inborn genetic diseases [RCV004428302]	uncertain significance	16	89694971	89694971	Human	1	name
405722303	CV3292862	single nucleotide variant	NM_052988.5(CDK10):c.935C>T (p.Ala312Val)	Inborn genetic diseases [RCV004428303]	uncertain significance	16	89695295	89695295	Human	1	name
405854711	CV3394818	single nucleotide variant	NM_052988.5(CDK10):c.669G>A (p.Trp223Ter)	Al Kaissi syndrome [RCV004551158]	likely pathogenic	16	89694665	89694665	Human	1	name
596926909	CV3530958	single nucleotide variant	NM_052988.5(CDK10):c.893G>A (p.Arg298His)	not provided [RCV004778543]	uncertain significance	16	89695031	89695031	Human		name
597655549	CV3642087	single nucleotide variant	NM_052988.5(CDK10):c.522G>C (p.Lys174Asn)	Inborn genetic diseases [RCV004976247]	likely benign	16	89693310	89693310	Human	1	name
597655523	CV3642091	single nucleotide variant	NM_052988.5(CDK10):c.443T>C (p.Leu148Pro)	Inborn genetic diseases [RCV004976251]	uncertain significance	16	89692474	89692474	Human	1	name
597631629	CV3642092	single nucleotide variant	NM_052988.5(CDK10):c.914T>C (p.Met305Thr)	Inborn genetic diseases [RCV004967750]	uncertain significance	16	89695052	89695052	Human	1	name
597655517	CV3642093	single nucleotide variant	NM_052988.5(CDK10):c.923C>T (p.Pro308Leu)	Inborn genetic diseases [RCV004976252]	uncertain significance	16	89695061	89695061	Human	1	name
597655495	CV3642094	single nucleotide variant	NM_052988.5(CDK10):c.350T>C (p.Met117Thr)	Inborn genetic diseases [RCV004976253]	uncertain significance	16	89691820	89691820	Human	1	name
597655489	CV3642095	single nucleotide variant	NM_052988.5(CDK10):c.772C>T (p.Pro258Ser)	Inborn genetic diseases [RCV004976254]	uncertain significance	16	89694768	89694768	Human	1	name
597655482	CV3642096	single nucleotide variant	NM_052988.5(CDK10):c.844T>A (p.Tyr282Asn)	Inborn genetic diseases [RCV004976255]	uncertain significance	16	89694982	89694982	Human	1	name
12858887	CV389169	single nucleotide variant	NM_052988.5(CDK10):c.725C>G (p.Thr242Ser)	Abnormal brain morphology [RCV000454194]	likely pathogenic	16	89694721	89694721	Human	1	name
598210061	CV3895022	single nucleotide variant	NM_052988.5(CDK10):c.613C>T (p.Arg205Ter)	Al Kaissi syndrome [RCV005358481]	likely pathogenic	16	89694177	89694177	Human	1	name
598179008	CV3943616	single nucleotide variant	NM_052988.5(CDK10):c.953T>G (p.Leu318Arg)	Inborn genetic diseases [RCV005310440]	uncertain significance	16	89695313	89695313	Human	1	name
598179014	CV3943617	single nucleotide variant	NM_052988.5(CDK10):c.587C>T (p.Thr196Ile)	Inborn genetic diseases [RCV005310441]	uncertain significance	16	89693446	89693446	Human	1	name
598179017	CV3943618	single nucleotide variant	NM_052988.5(CDK10):c.566G>C (p.Gly189Ala)	Inborn genetic diseases [RCV005310442]	uncertain significance	16	89693425	89693425	Human	1	name
598179024	CV3943620	single nucleotide variant	NM_052988.5(CDK10):c.829C>T (p.Leu277Phe)	Inborn genetic diseases [RCV005310443]	uncertain significance	16	89694967	89694967	Human	1	name
598179028	CV3943621	single nucleotide variant	NM_052988.5(CDK10):c.556C>G (p.Arg186Gly)	Inborn genetic diseases [RCV005310444]	uncertain significance	16	89693415	89693415	Human	1	name
598178994	CV3947558	single nucleotide variant	NM_052988.5(CDK10):c.536C>G (p.Thr179Arg)	Inborn genetic diseases [RCV005310437]	uncertain significance	16	89693324	89693324	Human	1	name
598179000	CV3947559	single nucleotide variant	NM_052988.5(CDK10):c.517G>A (p.Asp173Asn)	Inborn genetic diseases [RCV005310438]	uncertain significance	16	89693305	89693305	Human	1	name
598179002	CV3947560	single nucleotide variant	NM_052988.5(CDK10):c.967T>A (p.Phe323Ile)	Inborn genetic diseases [RCV005310439]	uncertain significance	16	89695327	89695327	Human	1	name
405654141	CV974031	single nucleotide variant	NM_052988.5(CDK10):c.691G>A (p.Glu231Lys)	not provided [RCV005001456]\|not specified [RCV003994853]	uncertain significance	16	89694687	89694687	Human		name
126736861	CV1018211	single nucleotide variant	NM_052988.5(CDK10):c.1065C>A (p.Ser355Arg)	Al Kaissi syndrome [RCV001328631]	uncertain significance	16	89695674	89695674	Human	1	name
153304698	CV1687240	single nucleotide variant	NM_052988.5(CDK10):c.1073G>A (p.Cys358Tyr)	not provided [RCV002262528]	likely benign	16	89695682	89695682	Human	2	name
153304698	CV1687240	single nucleotide variant	NM_052988.5(CDK10):c.1073G>A (p.Cys358Tyr)	not provided [RCV002262528]	likely benign	16	89695682	89695683	Human	2	name
156081136	CV2301057	single nucleotide variant	NM_052988.5(CDK10):c.1042C>T (p.Pro348Ser)	Inborn genetic diseases [RCV002887449]	uncertain significance	16	89695651	89695651	Human	1	name
155925037	CV2358257	single nucleotide variant	NM_052988.5(CDK10):c.1069C>T (p.Arg357Cys)	Inborn genetic diseases [RCV002992492]	uncertain significance	16	89695678	89695678	Human	1	name
156003345	CV2396724	single nucleotide variant	NM_052988.5(CDK10):c.1049C>T (p.Thr350Ile)	Inborn genetic diseases [RCV002734347]	uncertain significance	16	89695658	89695658	Human	1	name
329357705	CV2427809	single nucleotide variant	NM_052988.5(CDK10):c.1034G>A (p.Arg345Gln)	Inborn genetic diseases [RCV003178706]	uncertain significance	16	89695643	89695643	Human	1	name
401736980	CV2699642	single nucleotide variant	NM_052988.5(CDK10):c.1078C>A (p.Pro360Thr)	Inborn genetic diseases [RCV003250167]	uncertain significance	16	89695687	89695687	Human	1	name
401903623	CV2814609	single nucleotide variant	NM_052988.5(CDK10):c.1043C>A (p.Pro348Gln)	not provided [RCV003419536]	likely benign	16	89695652	89695652	Human		name
408381452	CV3523873	single nucleotide variant	NM_052988.5(CDK10):c.1054G>A (p.Glu352Lys)	not provided [RCV004766271]	uncertain significance	16	89695663	89695663	Human		name
597655556	CV3642086	single nucleotide variant	NM_052988.5(CDK10):c.1025G>A (p.Arg342His)	Inborn genetic diseases [RCV004976246]	uncertain significance	16	89695634	89695634	Human	1	name
598129068	CV3886872	single nucleotide variant	NM_052988.5(CDK10):c.1039G>A (p.Ala347Thr)	not provided [RCV005244532]	likely benign	16	89695648	89695648	Human		name
12858997	CV389170	single nucleotide variant	NM_052988.5(CDK10):c.1070G>A (p.Arg357His)	Abnormal brain morphology [RCV000454330]\|Al Kaissi syndrome [RCV003329117]\|Inborn genetic diseases [RCV002526371]	pathogenic\|likely pathogenic\|uncertain significance	16	89695679	89695679	Human	3	name
597656417	CV3552373	microsatellite	NM_052988.5(CDK10):c.202AAG[1] (p.Lys69del)	Al Kaissi syndrome [RCV004821231]	uncertain significance	16	89690593	89690595	Human		name
127286145	CV1161847	deletion	NM_052988.5(CDK10):c.870_871del (p.Trp291fs)	Al Kaissi syndrome [RCV001526542]\|Inborn genetic diseases [RCV002568129]\|not provided [RCV001658236]	pathogenic\|likely pathogenic	16	89695008	89695009	Human	2	name
150337029	CV1166212	deletion	NM_052988.5(CDK10):c.520_521del (p.Lys174fs)	Al Kaissi syndrome [RCV005253855]\|not provided [RCV001532331]	pathogenic	16	89693308	89693309	Human	1	name
152980893	CV1676205	duplication	NM_052988.5(CDK10):c.299_300dup (p.Leu101fs)	Al Kaissi syndrome [RCV002245281]	likely pathogenic	16	89691507	89691508	Human	1	name
155797514	CV1859386	deletion	NM_052988.5(CDK10):c.716_728del (p.Leu239fs)	Al Kaissi syndrome [RCV002465013]	pathogenic	16	89694708	89694720	Human	1	name
401830057	CV2747729	microsatellite	NM_052988.5(CDK10):c.625CTG[1] (p.Leu211del)	Al Kaissi syndrome [RCV003329147]	pathogenic	16	89694189	89694191	Human		name
21404476	CV802215	deletion	NM_052988.5(CDK10):c.550_556del (p.Leu184fs)	Al Kaissi syndrome [RCV001004864]	likely pathogenic	16	89693408	89693414	Human	1	name
34890439	CV904316	deletion	NM_052988.5(CDK10):c.664_665del (p.Met222fs)	Al Kaissi syndrome [RCV003329119]\|not provided [RCV001171589]	pathogenic	16	89694228	89694229	Human	1	name

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