Csnk1g1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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41 records found for search term Csnk1g1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
598128901	CV3886702	single nucleotide variant	NM_022048.5(CSNK1G1):c.*26C>T	not provided [RCV005244362]	benign	15	64171905	64171905	Human		name
8584523	CV119096	single nucleotide variant	NM_022048.3(CSNK1G1):c.-225+11729T>G	Lung cancer [RCV000099616]	uncertain significance	15	64344259	64344259	Human		name
405263723	CV3185222	single nucleotide variant	NM_022048.5(CSNK1G1):c.96A>G (p.Ser32=)	not provided [RCV003885786]	likely benign	15	64300404	64300404	Human		name
8635532	CV90753	single nucleotide variant	NM_022048.3(CSNK1G1):c.102C>T (p.Ser34=)	Malignant melanoma [RCV000070851]	not provided	15	64300398	64300398	Human		name
152980428	CV1678611	single nucleotide variant	NM_022048.5(CSNK1G1):c.80G>A (p.Arg27Gln)	not specified [RCV002247119]	uncertain significance	15	64300420	64300420	Human		name
156302148	CV2258612	single nucleotide variant	NM_022048.5(CSNK1G1):c.79C>G (p.Arg27Gly)	not specified [RCV004116085]	uncertain significance	15	64300421	64300421	Human		name
405687274	CV3236270	single nucleotide variant	NM_022048.5(CSNK1G1):c.43A>C (p.Thr15Pro)	not specified [RCV004372594]	uncertain significance	15	64300457	64300457	Human		name
617149302	CV4021485	single nucleotide variant	NM_022048.5(CSNK1G1):c.420G>A (p.Thr140=)	not provided [RCV005425454]	likely benign	15	64216586	64216586	Human		name
329361772	CV2468295	single nucleotide variant	NM_022048.5(CSNK1G1):c.190C>T (p.Leu64Phe)	not specified [RCV004275852]	uncertain significance	15	64259233	64259233	Human		name
405687268	CV3236269	single nucleotide variant	NM_022048.5(CSNK1G1):c.200A>G (p.Asn67Ser)	not specified [RCV004372593]	uncertain significance	15	64259223	64259223	Human		name
407465388	CV3430004	single nucleotide variant	NM_022048.5(CSNK1G1):c.206A>G (p.Tyr69Cys)	not specified [RCV004613691]	uncertain significance	15	64259217	64259217	Human		name
598129843	CV3887265	single nucleotide variant	NM_022048.5(CSNK1G1):c.143A>G (p.Lys48Arg)	not provided [RCV005245325]	uncertain significance	15	64300357	64300357	Human		name
598225591	CV3892392	duplication	NM_022048.5(CSNK1G1):c.932dup (p.Thr312fs)	CSNK1G1-related developmental disorder with autism spectrum disorder [RCV005254227]	likely pathogenic	15	64204507	64204508	Human		name , trait
151353192	CV1326158	single nucleotide variant	NM_022048.5(CSNK1G1):c.520C>T (p.Arg174Ter)	not provided [RCV001816157]	uncertain significance	15	64214049	64214049	Human		name
151662292	CV1333011	single nucleotide variant	NM_022048.5(CSNK1G1):c.368C>G (p.Pro123Arg)	See cases [RCV001837243]	uncertain significance	15	64216638	64216638	Human		name
8696229	CV150143	single nucleotide variant	NM_022048.5(CSNK1G1):c.688C>T (p.Arg230Trp)	not provided [RCV000128638]	uncertain significance	15	64207586	64207586	Human		name
152042101	CV1669958	single nucleotide variant	NM_022048.5(CSNK1G1):c.488G>T (p.Arg163Leu)	not provided [RCV002224860]	uncertain significance	15	64214081	64214081	Human		name
156376554	CV1869005	single nucleotide variant	NM_022048.5(CSNK1G1):c.587A>G (p.Asp196Gly)	not provided [RCV003066781]	uncertain significance	15	64213982	64213982	Human		name
156120431	CV2354165	single nucleotide variant	NM_022048.5(CSNK1G1):c.314A>G (p.Tyr105Cys)	not specified [RCV004206599]	uncertain significance	15	64216692	64216692	Human		name
156131190	CV2358214	single nucleotide variant	NM_022048.5(CSNK1G1):c.515T>C (p.Ile172Thr)	not specified [RCV004212009]	uncertain significance	15	64214054	64214054	Human		name
401753903	CV2719105	single nucleotide variant	NM_022048.5(CSNK1G1):c.440A>G (p.Gln147Arg)	not specified [RCV004324778]	uncertain significance	15	64216566	64216566	Human		name
401782280	CV2719266	single nucleotide variant	NM_022048.5(CSNK1G1):c.553A>G (p.Ile185Val)	not specified [RCV004324909]	uncertain significance	15	64214016	64214016	Human		name
401930031	CV2814224	single nucleotide variant	NM_022048.5(CSNK1G1):c.985G>A (p.Val329Ile)	not provided [RCV003390517]	likely benign	15	64204455	64204455	Human		name
405687279	CV3236271	single nucleotide variant	NM_022048.5(CSNK1G1):c.521G>C (p.Arg174Pro)	not specified [RCV004372595]	uncertain significance	15	64214048	64214048	Human		name
405687287	CV3236273	single nucleotide variant	NM_022048.5(CSNK1G1):c.767C>G (p.Ala256Gly)	not specified [RCV004372597]	uncertain significance	15	64204948	64204948	Human		name
405687293	CV3236274	single nucleotide variant	NM_022048.5(CSNK1G1):c.931T>C (p.Phe311Leu)	not specified [RCV004372598]	uncertain significance	15	64204509	64204509	Human		name
597805066	CV3654700	single nucleotide variant	NM_022048.5(CSNK1G1):c.986T>C (p.Val329Ala)	not specified [RCV004908272]	uncertain significance	15	64204454	64204454	Human		name
597805068	CV3654701	single nucleotide variant	NM_022048.5(CSNK1G1):c.343G>A (p.Ala115Thr)	not specified [RCV004908273]	uncertain significance	15	64216663	64216663	Human		name
597805071	CV3654703	single nucleotide variant	NM_022048.5(CSNK1G1):c.872G>A (p.Arg291Gln)	not specified [RCV004908275]	uncertain significance	15	64204568	64204568	Human		name
598218974	CV3959412	single nucleotide variant	NM_022048.5(CSNK1G1):c.923G>A (p.Arg308Gln)	not specified [RCV005317323]	uncertain significance	15	64204517	64204517	Human		name
616939820	CV4014463	single nucleotide variant	NM_022048.5(CSNK1G1):c.997A>G (p.Ile333Val)	not provided [RCV005413957]	uncertain significance	15	64204443	64204443	Human		name
617149888	CV4021287	single nucleotide variant	NM_022048.5(CSNK1G1):c.592G>A (p.Glu198Lys)	not provided [RCV005425256]	uncertain significance	15	64213977	64213977	Human		name
329365049	CV2439986	single nucleotide variant	NM_022048.5(CSNK1G1):c.1100G>A (p.Arg367Gln)	not specified [RCV004260465]	uncertain significance	15	64203089	64203089	Human		name
329389028	CV2469740	single nucleotide variant	NM_022048.5(CSNK1G1):c.1109T>C (p.Val370Ala)	not specified [RCV004284935]	uncertain significance	15	64180453	64180453	Human		name
405687250	CV3236265	single nucleotide variant	NM_022048.5(CSNK1G1):c.1045A>G (p.Ile349Val)	not specified [RCV004372589]	uncertain significance	15	64203144	64203144	Human		name
405687254	CV3236266	single nucleotide variant	NM_022048.5(CSNK1G1):c.1108G>A (p.Val370Met)	not specified [RCV004372590]	uncertain significance	15	64180454	64180454	Human		name
405687260	CV3236267	single nucleotide variant	NM_022048.5(CSNK1G1):c.1189G>A (p.Glu397Lys)	not specified [RCV004372591]	uncertain significance	15	64180373	64180373	Human		name
405687265	CV3236268	single nucleotide variant	NM_022048.5(CSNK1G1):c.1259G>A (p.Arg420His)	not specified [RCV004372592]	uncertain significance	15	64171941	64171941	Human		name
596926030	CV3536069	single nucleotide variant	NM_022048.5(CSNK1G1):c.1103A>G (p.Asn368Ser)	Neurodevelopmental disorder [RCV004788499]	uncertain significance	15	64203086	64203086	Human	1	name
597880561	CV3826403	single nucleotide variant	NM_022048.5(CSNK1G1):c.1250C>T (p.Thr417Ile)	not provided [RCV005178100]	uncertain significance	15	64171950	64171950	Human		name
598129827	CV3887249	single nucleotide variant	NM_022048.5(CSNK1G1):c.1166A>G (p.Asn389Ser)	not provided [RCV005245309]	likely benign	15	64180396	64180396	Human		name

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