Snw1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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29 records found for search term Snw1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405732238	CV3326364	single nucleotide variant	NM_012245.3(SNW1):c.89G>A (p.Arg30Gln)	not specified [RCV004464488]	uncertain significance	14	77755046	77755046	Human		name
598171901	CV3911646	single nucleotide variant	NM_012245.3(SNW1):c.40T>C (p.Ser14Pro)	not specified [RCV005284882]	uncertain significance	14	77755095	77755095	Human		name
155948360	CV2272107	single nucleotide variant	NM_012245.3(SNW1):c.192T>G (p.Phe64Leu)	not specified [RCV004124892]	uncertain significance	14	77751457	77751457	Human		name
156395264	CV2325361	single nucleotide variant	NM_012245.3(SNW1):c.293A>C (p.Tyr98Ser)	not specified [RCV004177739]	uncertain significance	14	77751356	77751356	Human		name
156263561	CV2329384	single nucleotide variant	NM_012245.3(SNW1):c.295G>A (p.Asp99Asn)	not specified [RCV004187398]	uncertain significance	14	77751354	77751354	Human		name
407503792	CV3474693	single nucleotide variant	NM_012245.3(SNW1):c.204T>G (p.His68Gln)	not specified [RCV004670368]	uncertain significance	14	77751445	77751445	Human		name
597740994	CV3607214	single nucleotide variant	NM_012245.3(SNW1):c.133G>A (p.Gly45Arg)	not specified [RCV004864770]	uncertain significance	14	77755002	77755002	Human		name
597745167	CV3607217	single nucleotide variant	NM_012245.3(SNW1):c.140G>A (p.Arg47Gln)	not specified [RCV004865617]	uncertain significance	14	77754995	77754995	Human		name
156104533	CV2207452	single nucleotide variant	NM_012245.3(SNW1):c.475G>A (p.Val159Ile)	not specified [RCV004089936]	uncertain significance	14	77738836	77738836	Human		name
156343782	CV2232893	single nucleotide variant	NM_012245.3(SNW1):c.606G>A (p.Met202Ile)	not specified [RCV004101499]	uncertain significance	14	77737003	77737003	Human		name
156114775	CV2273207	single nucleotide variant	NM_012245.3(SNW1):c.830C>T (p.Thr277Ile)	not specified [RCV004138140]	uncertain significance	14	77732546	77732546	Human		name
329401559	CV2461048	single nucleotide variant	NM_012245.3(SNW1):c.912G>A (p.Met304Ile)	not specified [RCV004265200]	uncertain significance	14	77731109	77731109	Human		name
405732224	CV3326362	single nucleotide variant	NM_012245.3(SNW1):c.301A>G (p.Ile101Val)	not specified [RCV004464486]	uncertain significance	14	77751348	77751348	Human		name
405732230	CV3326363	single nucleotide variant	NM_012245.3(SNW1):c.875A>G (p.Tyr292Cys)	not specified [RCV004464487]	uncertain significance	14	77732501	77732501	Human		name
407503787	CV3474692	single nucleotide variant	NM_012245.3(SNW1):c.619A>G (p.Met207Val)	not specified [RCV004670367]	uncertain significance	14	77736990	77736990	Human		name
597740998	CV3607216	single nucleotide variant	NM_012245.3(SNW1):c.500C>T (p.Ala167Val)	not specified [RCV004864771]	uncertain significance	14	77738811	77738811	Human		name
13706095	CV537235	single nucleotide variant	NM_012245.3(SNW1):c.584G>T (p.Arg195Met)	not provided [RCV000658702]	uncertain significance	14	77737025	77737025	Human		name
156290696	CV2342691	single nucleotide variant	NM_012245.3(SNW1):c.1154A>G (p.Asn385Ser)	not specified [RCV004196772]	uncertain significance	14	77720805	77720805	Human		name
401765986	CV2683492	single nucleotide variant	NM_012245.3(SNW1):c.1208A>G (p.Asn403Ser)	not specified [RCV004288244]	uncertain significance	14	77720751	77720751	Human		name
401896454	CV2781402	single nucleotide variant	NM_012245.3(SNW1):c.1090C>G (p.Gln364Glu)	not specified [RCV004352405]	uncertain significance	14	77723221	77723221	Human		name
405732205	CV3326360	single nucleotide variant	NM_012245.3(SNW1):c.1340T>C (p.Ile447Thr)	not specified [RCV004464484]	uncertain significance	14	77718439	77718439	Human		name
405732216	CV3326361	single nucleotide variant	NM_012245.3(SNW1):c.1448G>A (p.Arg483His)	not specified [RCV004464485]	uncertain significance	14	77718251	77718251	Human		name
407503795	CV3474694	single nucleotide variant	NM_012245.3(SNW1):c.1436C>G (p.Ser479Cys)	not specified [RCV004670369]	uncertain significance	14	77718263	77718263	Human		name
407503798	CV3484773	single nucleotide variant	NM_012245.3(SNW1):c.1049G>A (p.Arg350His)	not specified [RCV004670370]	uncertain significance	14	77723262	77723262	Human		name
407525300	CV3484774	single nucleotide variant	NM_012245.3(SNW1):c.1270G>T (p.Gly424Cys)	not specified [RCV004679122]	uncertain significance	14	77718509	77718509	Human		name
597745162	CV3607215	single nucleotide variant	NM_012245.3(SNW1):c.1198C>T (p.Arg400Trp)	not specified [RCV004865616]	uncertain significance	14	77720761	77720761	Human		name
597745171	CV3607218	single nucleotide variant	NM_012245.3(SNW1):c.1556A>T (p.Asp519Val)	not specified [RCV004865618]	uncertain significance	14	77718143	77718143	Human		name
598171905	CV3911645	single nucleotide variant	NM_012245.3(SNW1):c.1165A>G (p.Ser389Gly)	not specified [RCV005284881]	uncertain significance	14	77720794	77720794	Human		name
598171896	CV3911647	single nucleotide variant	NM_012245.3(SNW1):c.1199G>A (p.Arg400Gln)	not specified [RCV005284883]	uncertain significance	14	77720760	77720760	Human		name

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