Haus4 Variant Search Result - Rat Genome Database

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27 records found for search term Haus4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405789321	CV3266194	single nucleotide variant	NM_001166269.2(HAUS4):c.22T>C (p.Ser8Pro)	not specified [RCV004399204]	uncertain significance	14	22955133	22955133	Human		name
405789325	CV3266195	single nucleotide variant	NM_001166269.2(HAUS4):c.23C>T (p.Ser8Leu)	not specified [RCV004399205]	likely benign	14	22955132	22955132	Human		name
407514218	CV3444022	single nucleotide variant	NM_001166269.2(HAUS4):c.266A>C (p.Gln89Pro)	not specified [RCV004627479]	uncertain significance	14	22952392	22952392	Human		name
156135615	CV2245611	single nucleotide variant	NM_001166269.2(HAUS4):c.533C>T (p.Thr178Ile)	not specified [RCV004111506]	uncertain significance	14	22950343	22950343	Human		name
155987718	CV2275680	single nucleotide variant	NM_001166269.2(HAUS4):c.439C>T (p.Leu147Phe)	not specified [RCV004137295]	uncertain significance	14	22951581	22951581	Human		name
156285526	CV2317640	single nucleotide variant	NM_001166269.2(HAUS4):c.392G>A (p.Ser131Asn)	not specified [RCV004172576]	uncertain significance	14	22951628	22951628	Human		name
156223133	CV2394845	single nucleotide variant	NM_001166269.2(HAUS4):c.868A>T (p.Thr290Ser)	not specified [RCV004234505]	uncertain significance	14	22947211	22947211	Human		name
329367152	CV2427245	single nucleotide variant	NM_001166269.2(HAUS4):c.569A>C (p.Asp190Ala)	not specified [RCV004248113]	uncertain significance	14	22948007	22948007	Human		name
329372352	CV2443118	single nucleotide variant	NM_001166269.2(HAUS4):c.914G>A (p.Arg305His)	not specified [RCV004255320]	uncertain significance	14	22946703	22946703	Human		name
401754682	CV2719674	single nucleotide variant	NM_001166269.2(HAUS4):c.664G>A (p.Glu222Lys)	not specified [RCV004329119]	uncertain significance	14	22947912	22947912	Human		name
401876280	CV2789223	single nucleotide variant	NM_001166269.2(HAUS4):c.310G>T (p.Val104Leu)	not specified [RCV004365258]	likely benign	14	22952348	22952348	Human		name
405789329	CV3266196	single nucleotide variant	NM_001166269.2(HAUS4):c.434C>T (p.Ala145Val)	not specified [RCV004399206]	uncertain significance	14	22951586	22951586	Human		name
405789333	CV3266197	single nucleotide variant	NM_001166269.2(HAUS4):c.477G>C (p.Trp159Cys)	not specified [RCV004399207]	uncertain significance	14	22950399	22950399	Human		name
405789337	CV3266198	single nucleotide variant	NM_001166269.2(HAUS4):c.976T>G (p.Ser326Ala)	not specified [RCV004399208]	uncertain significance	14	22946641	22946641	Human		name
407504743	CV3444020	single nucleotide variant	NM_001166269.2(HAUS4):c.899G>A (p.Arg300His)	not specified [RCV004624134]	uncertain significance	14	22947180	22947180	Human		name
407514216	CV3444021	single nucleotide variant	NM_001166269.2(HAUS4):c.580G>A (p.Val194Met)	not specified [RCV004627478]	uncertain significance	14	22947996	22947996	Human		name
407504747	CV3444023	single nucleotide variant	NM_001166269.2(HAUS4):c.337G>A (p.Glu113Lys)	not specified [RCV004624135]	uncertain significance	14	22951683	22951683	Human		name
597709676	CV3682180	single nucleotide variant	NM_001166269.2(HAUS4):c.395A>G (p.Gln132Arg)	not specified [RCV004917346]	uncertain significance	14	22951625	22951625	Human		name
597781277	CV3682181	single nucleotide variant	NM_001166269.2(HAUS4):c.299A>G (p.Gln100Arg)	not specified [RCV004930854]	uncertain significance	14	22952359	22952359	Human		name
597781280	CV3682182	single nucleotide variant	NM_001166269.2(HAUS4):c.865G>A (p.Asp289Asn)	not specified [RCV004930855]	uncertain significance	14	22947214	22947214	Human		name
597709685	CV3682183	single nucleotide variant	NM_001166269.2(HAUS4):c.613G>T (p.Val205Phe)	not specified [RCV004917347]	uncertain significance	14	22947963	22947963	Human		name
597781284	CV3682184	single nucleotide variant	NM_001166269.2(HAUS4):c.422G>A (p.Gly141Glu)	not specified [RCV004930856]	uncertain significance	14	22951598	22951598	Human		name
598246388	CV3971422	single nucleotide variant	NM_001166269.2(HAUS4):c.874A>G (p.Thr292Ala)	not specified [RCV005345146]	uncertain significance	14	22947205	22947205	Human		name
15104795	CV725618	single nucleotide variant	NM_001166269.2(HAUS4):c.548A>G (p.Tyr183Cys)	not provided [RCV000892954]	benign	14	22950328	22950328	Human		name
156071531	CV2381392	single nucleotide variant	NM_001166269.2(HAUS4):c.1048A>C (p.Asn350His)	not specified [RCV004227441]	uncertain significance	14	22946569	22946569	Human		name
598265537	CV3971419	single nucleotide variant	NM_001166269.2(HAUS4):c.1049A>G (p.Asn350Ser)	not specified [RCV005349076]	uncertain significance	14	22946568	22946568	Human		name
598265549	CV3971421	single nucleotide variant	NM_001166269.2(HAUS4):c.1087C>T (p.Arg363Cys)	not specified [RCV005349078]	uncertain significance	14	22946530	22946530	Human		name

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