Csk Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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47 records found for search term Csk

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8627701	CV82845	single nucleotide variant	NM_001127190.1(CSK):c.129+29C>T	Malignant melanoma [RCV000062925]	not provided	15	74798757	74798757	Human		name
401904547	CV2814328	single nucleotide variant	NM_004383.3(CSK):c.264A>C (p.Thr88=)	not provided [RCV003395002]	likely benign	15	74799293	74799293	Human		name
405677415	CV3236033	single nucleotide variant	NM_004383.3(CSK):c.64G>A (p.Gly22Ser)	not specified [RCV004370374]	uncertain significance	15	74798663	74798663	Human		name
401763441	CV2720324	single nucleotide variant	NM_004383.3(CSK):c.296C>T (p.Pro99Leu)	not specified [RCV004325647]	uncertain significance	15	74799325	74799325	Human		name
405677399	CV3236030	single nucleotide variant	NM_004383.3(CSK):c.138C>G (p.Asn46Lys)	not specified [RCV004370371]	uncertain significance	15	74798834	74798834	Human		name
405677405	CV3236031	single nucleotide variant	NM_004383.3(CSK):c.193G>A (p.Val65Ile)	not specified [RCV004370372]	uncertain significance	15	74798889	74798889	Human		name
405677410	CV3236032	single nucleotide variant	NM_004383.3(CSK):c.281G>A (p.Arg94Gln)	not specified [RCV004370373]	uncertain significance	15	74799310	74799310	Human		name
407464947	CV3429897	single nucleotide variant	NM_004383.3(CSK):c.167G>A (p.Arg56His)	not specified [RCV004613584]	uncertain significance	15	74798863	74798863	Human		name
597800139	CV3654461	single nucleotide variant	NM_004383.3(CSK):c.121G>A (p.Val41Ile)	not specified [RCV004905560]	uncertain significance	15	74798720	74798720	Human		name
597800152	CV3654467	single nucleotide variant	NM_004383.3(CSK):c.290A>G (p.Tyr97Cys)	not specified [RCV004905566]	likely benign	15	74799319	74799319	Human		name
156170168	CV2312487	single nucleotide variant	NM_004383.3(CSK):c.367G>A (p.Asp123Asn)	not specified [RCV004167452]	uncertain significance	15	74799396	74799396	Human		name
597800141	CV3654462	single nucleotide variant	NM_004383.3(CSK):c.661G>A (p.Val221Ile)	not specified [RCV004905561]	uncertain significance	15	74800861	74800861	Human		name
597800150	CV3654466	single nucleotide variant	NM_004383.3(CSK):c.653A>G (p.Lys218Arg)	not specified [RCV004905565]	uncertain significance	15	74800853	74800853	Human		name
598260995	CV3963184	single nucleotide variant	NM_004383.3(CSK):c.670A>G (p.Ile224Val)	not specified [RCV005325084]	uncertain significance	15	74800870	74800870	Human		name
598261004	CV3963186	single nucleotide variant	NM_004383.3(CSK):c.448A>G (p.Met150Val)	not specified [RCV005325086]	uncertain significance	15	74799477	74799477	Human		name
15179435	CV726252	single nucleotide variant	NM_004383.3(CSK):c.860G>A (p.Gly287Asp)	not provided [RCV000885289]	benign	15	74801568	74801568	Human		name
156265003	CV2198620	single nucleotide variant	NM_004383.3(CSK):c.1208A>G (p.Tyr403Cys)	not specified [RCV004075637]	uncertain significance	15	74802368	74802368	Human		name
156359423	CV2328199	single nucleotide variant	NM_004383.3(CSK):c.1034C>T (p.Thr345Met)	not specified [RCV004173293]	uncertain significance	15	74801841	74801841	Human		name
405263473	CV3185137	single nucleotide variant	NM_004383.3(CSK):c.1282G>A (p.Ala428Thr)	not provided [RCV003885701]	benign	15	74802442	74802442	Human		name
597800143	CV3654463	single nucleotide variant	NM_004383.3(CSK):c.1219G>A (p.Ala407Thr)	not specified [RCV004905562]	uncertain significance	15	74802379	74802379	Human		name
597800145	CV3654464	single nucleotide variant	NM_004383.3(CSK):c.1228G>A (p.Gly410Ser)	not specified [RCV004905563]	uncertain significance	15	74802388	74802388	Human		name
598261000	CV3963185	single nucleotide variant	NM_004383.3(CSK):c.1251A>C (p.Glu417Asp)	not specified [RCV005325085]	uncertain significance	15	74802411	74802411	Human		name
405677468	CV3236044	single nucleotide variant	NM_001043229.2(CSKMT):c.91G>A (p.Ala31Thr)	not specified [RCV004370385]	uncertain significance	11	62666419	62666419	Human		name
405677420	CV3236034	single nucleotide variant	NM_001043229.2(CSKMT):c.233G>C (p.Arg78Pro)	not specified [RCV004370375]	uncertain significance	11	62666561	62666561	Human		name
405677424	CV3236035	single nucleotide variant	NM_001043229.2(CSKMT):c.248G>C (p.Gly83Ala)	not specified [RCV004370376]	uncertain significance	11	62666576	62666576	Human		name
405677429	CV3236036	single nucleotide variant	NM_001043229.2(CSKMT):c.268T>C (p.Cys90Arg)	not specified [RCV004370377]	uncertain significance	11	62666596	62666596	Human		name
407478168	CV3429898	single nucleotide variant	NM_001043229.2(CSKMT):c.229C>G (p.Leu77Val)	not specified [RCV004613585]	uncertain significance	11	62666557	62666557	Human		name
407478179	CV3429900	single nucleotide variant	NM_001043229.2(CSKMT):c.184G>C (p.Gly62Arg)	not specified [RCV004613587]	uncertain significance	11	62666512	62666512	Human		name
598261015	CV3963188	single nucleotide variant	NM_001043229.2(CSKMT):c.196C>G (p.Pro66Ala)	not specified [RCV005325088]	uncertain significance	11	62666524	62666524	Human		name
598261025	CV3963190	single nucleotide variant	NM_001043229.2(CSKMT):c.257C>T (p.Thr86Ile)	not specified [RCV005325090]	uncertain significance	11	62666585	62666585	Human		name
598261030	CV3963191	single nucleotide variant	NM_001043229.2(CSKMT):c.211G>A (p.Ala71Thr)	not specified [RCV005325091]	uncertain significance	11	62666539	62666539	Human		name
598261036	CV3963192	single nucleotide variant	NM_001043229.2(CSKMT):c.131G>A (p.Arg44His)	not specified [RCV005325092]	uncertain significance	11	62666459	62666459	Human		name
15148591	CV738084	single nucleotide variant	NM_001043229.2(CSKMT):c.181C>T (p.Gln61Ter)	not provided [RCV000900751]	benign	11	62666509	62666509	Human		name
401746432	CV2731797	single nucleotide variant	NM_001043229.2(CSKMT):c.556A>G (p.Arg186Gly)	not specified [RCV004333050]	uncertain significance	11	62666884	62666884	Human		name
401877559	CV2790212	single nucleotide variant	NM_001043229.2(CSKMT):c.650C>G (p.Thr217Ser)	not specified [RCV004364127]	uncertain significance	11	62666978	62666978	Human		name
405677434	CV3236037	single nucleotide variant	NM_001043229.2(CSKMT):c.347T>G (p.Met116Arg)	not specified [RCV004370378]	uncertain significance	11	62666675	62666675	Human		name
405677442	CV3236039	single nucleotide variant	NM_001043229.2(CSKMT):c.353G>T (p.Ser118Ile)	not specified [RCV004370380]	uncertain significance	11	62666681	62666681	Human		name
405677448	CV3236040	single nucleotide variant	NM_001043229.2(CSKMT):c.398A>G (p.His133Arg)	not specified [RCV004370381]	uncertain significance	11	62666726	62666726	Human		name
405677453	CV3236041	single nucleotide variant	NM_001043229.2(CSKMT):c.511C>T (p.Arg171Trp)	not specified [RCV004370382]	uncertain significance	11	62666839	62666839	Human		name
405677457	CV3236042	single nucleotide variant	NM_001043229.2(CSKMT):c.512G>C (p.Arg171Pro)	not specified [RCV004370383]	uncertain significance	11	62666840	62666840	Human		name
405677461	CV3236043	single nucleotide variant	NM_001043229.2(CSKMT):c.674C>T (p.Pro225Leu)	not specified [RCV004370384]	uncertain significance	11	62667002	62667002	Human		name
407478173	CV3429899	single nucleotide variant	NM_001043229.2(CSKMT):c.670G>C (p.Gly224Arg)	not specified [RCV004613586]	uncertain significance	11	62666998	62666998	Human		name
597800154	CV3654468	single nucleotide variant	NM_001043229.2(CSKMT):c.563T>G (p.Leu188Arg)	not specified [RCV004905567]	uncertain significance	11	62666891	62666891	Human		name
597800157	CV3654469	single nucleotide variant	NM_001043229.2(CSKMT):c.346A>G (p.Met116Val)	not specified [RCV004905568]	uncertain significance	11	62666674	62666674	Human		name
597800159	CV3654470	single nucleotide variant	NM_001043229.2(CSKMT):c.430G>A (p.Asp144Asn)	not specified [RCV004905569]	uncertain significance	11	62666758	62666758	Human		name
597800161	CV3654471	single nucleotide variant	NM_001043229.2(CSKMT):c.313G>T (p.Gly105Trp)	not specified [RCV004905570]	uncertain significance	11	62666641	62666641	Human		name
598261020	CV3963189	single nucleotide variant	NM_001043229.2(CSKMT):c.374G>C (p.Gly125Ala)	not specified [RCV005325089]	uncertain significance	11	62666702	62666702	Human		name

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