Csnk1a1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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31 records found for search term Csnk1a1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
21071113	CV794303	deletion	NM_001892.6(CSNK1A1):c.1105_1108del	CIC-rearranged sarcoma [RCV000993826]	not provided	5	149495745	149495748	Human		name
405687189	CV3236253	single nucleotide variant	NM_001892.6(CSNK1A1):c.947G>A (p.Gly316Asp)	not specified [RCV004372577]	uncertain significance	5	149505506	149505506	Human		name
407465362	CV3429996	single nucleotide variant	NM_001892.6(CSNK1A1):c.988A>T (p.Thr330Ser)	not specified [RCV004613683]	uncertain significance	5	149505465	149505465	Human		name
597805023	CV3654679	single nucleotide variant	NM_001892.6(CSNK1A1):c.959A>T (p.Gln320Leu)	not specified [RCV004908251]	uncertain significance	5	149505494	149505494	Human		name
8631478	CV86682	single nucleotide variant	NM_001025105.2(CSNK1A1):c.190T>G (p.Tyr64Asp)	Malignant melanoma [RCV000066773]	not provided	5	149550115	149550115	Human		name
405687205	CV3236256	single nucleotide variant	NM_145203.6(CSNK1A1L):c.13A>T (p.Ser5Cys)	not specified [RCV004372580]	uncertain significance	13	37105244	37105244	Human		name
401747586	CV2691628	single nucleotide variant	NM_145203.6(CSNK1A1L):c.43G>A (p.Gly15Arg)	not specified [RCV004305445]	uncertain significance	13	37105214	37105214	Human		name
401886077	CV2771604	single nucleotide variant	NM_145203.6(CSNK1A1L):c.62G>A (p.Arg21Gln)	not specified [RCV004350411]	uncertain significance	13	37105195	37105195	Human		name
597805035	CV3654685	single nucleotide variant	NM_145203.6(CSNK1A1L):c.58G>C (p.Val20Leu)	not specified [RCV004908257]	uncertain significance	13	37105199	37105199	Human		name
156277347	CV2300153	single nucleotide variant	NM_145203.6(CSNK1A1L):c.241C>A (p.Gln81Lys)	not specified [RCV004151343]	uncertain significance	13	37105016	37105016	Human		name
329400390	CV2441609	single nucleotide variant	NM_145203.6(CSNK1A1L):c.229C>T (p.His77Tyr)	not specified [RCV004259434]	uncertain significance	13	37105028	37105028	Human		name
405687199	CV3236255	single nucleotide variant	NM_145203.6(CSNK1A1L):c.106A>G (p.Thr36Ala)	not specified [RCV004372579]	uncertain significance	13	37105151	37105151	Human		name
405687210	CV3236257	single nucleotide variant	NM_145203.6(CSNK1A1L):c.158A>C (p.Lys53Thr)	not specified [RCV004372581]	uncertain significance	13	37105099	37105099	Human		name
597805027	CV3654681	single nucleotide variant	NM_145203.6(CSNK1A1L):c.146C>G (p.Ser49Cys)	not specified [RCV004908253]	uncertain significance	13	37105111	37105111	Human		name
597805029	CV3654682	single nucleotide variant	NM_145203.6(CSNK1A1L):c.172C>A (p.Leu58Met)	not specified [RCV004908254]	uncertain significance	13	37105085	37105085	Human		name
598261780	CV3959404	single nucleotide variant	NM_145203.6(CSNK1A1L):c.292G>C (p.Glu98Gln)	not specified [RCV005325246]	uncertain significance	13	37104965	37104965	Human		name
156386864	CV2225227	single nucleotide variant	NM_145203.6(CSNK1A1L):c.674G>C (p.Arg225Thr)	not specified [RCV004095022]	uncertain significance	13	37104583	37104583	Human		name
156050720	CV2304600	single nucleotide variant	NM_145203.6(CSNK1A1L):c.344T>G (p.Met115Arg)	not specified [RCV004166494]	uncertain significance	13	37104913	37104913	Human		name
156084207	CV2366027	single nucleotide variant	NM_145203.6(CSNK1A1L):c.541C>T (p.Leu181Phe)	not specified [RCV004208026]	uncertain significance	13	37104716	37104716	Human		name
405687215	CV3236258	single nucleotide variant	NM_145203.6(CSNK1A1L):c.845G>A (p.Arg282His)	not specified [RCV004372582]	uncertain significance	13	37104412	37104412	Human		name
405687220	CV3236259	single nucleotide variant	NM_145203.6(CSNK1A1L):c.919C>G (p.Gln307Glu)	not specified [RCV004372583]	uncertain significance	13	37104338	37104338	Human		name
407465366	CV3429997	single nucleotide variant	NM_145203.6(CSNK1A1L):c.653G>A (p.Ser218Asn)	not specified [RCV004613684]	uncertain significance	13	37104604	37104604	Human		name
597805031	CV3654683	single nucleotide variant	NM_145203.6(CSNK1A1L):c.556C>G (p.Arg186Gly)	not specified [RCV004908255]	uncertain significance	13	37104701	37104701	Human		name
597805033	CV3654684	single nucleotide variant	NM_145203.6(CSNK1A1L):c.404G>A (p.Arg135Gln)	not specified [RCV004908256]	uncertain significance	13	37104853	37104853	Human		name
597805038	CV3654686	single nucleotide variant	NM_145203.6(CSNK1A1L):c.335C>T (p.Thr112Ile)	not specified [RCV004908258]	uncertain significance	13	37104922	37104922	Human		name
597805040	CV3654687	single nucleotide variant	NM_145203.6(CSNK1A1L):c.330G>A (p.Met110Ile)	not specified [RCV004908259]	uncertain significance	13	37104927	37104927	Human		name
597805042	CV3654688	single nucleotide variant	NM_145203.6(CSNK1A1L):c.419A>G (p.Asp140Gly)	not specified [RCV004908260]	uncertain significance	13	37104838	37104838	Human		name
598261784	CV3959405	single nucleotide variant	NM_145203.6(CSNK1A1L):c.596G>C (p.Ser199Thr)	not specified [RCV005325247]	uncertain significance	13	37104661	37104661	Human		name
598261790	CV3959406	single nucleotide variant	NM_145203.6(CSNK1A1L):c.512A>C (p.Gln171Pro)	not specified [RCV005325248]	uncertain significance	13	37104745	37104745	Human		name
598261795	CV3959407	single nucleotide variant	NM_145203.6(CSNK1A1L):c.839T>A (p.Leu280Gln)	not specified [RCV005325249]	uncertain significance	13	37104418	37104418	Human		name
405687193	CV3236254	single nucleotide variant	NM_145203.6(CSNK1A1L):c.1001T>G (p.Val334Gly)	not specified [RCV004372578]	uncertain significance	13	37104256	37104256	Human		name

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