Bnip1 Variant Search Result - Rat Genome Database

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36 records found for search term Bnip1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150458199	CV1001332	single nucleotide variant	NM_001205.3(BNIP1):c.84+3A>T	Spondyloepiphyseal dysplasia congenita [RCV001638059]	uncertain significance	5	173144632	173144632	Human	1	name
155990579	CV2255533	single nucleotide variant	NM_001205.3(BNIP1):c.178-2750C>T	not specified [RCV004119962]	uncertain significance	5	173151572	173151572	Human		name
155996809	CV2373117	single nucleotide variant	NM_001205.3(BNIP1):c.178-2669C>A	not specified [RCV004217809]	uncertain significance	5	173151653	173151653	Human		name
597719545	CV3643149	single nucleotide variant	NM_001205.3(BNIP1):c.178-2752T>C	not specified [RCV004887643]	uncertain significance	5	173151570	173151570	Human		name
598162621	CV3946221	single nucleotide variant	NM_001205.3(BNIP1):c.178-2726A>T	not specified [RCV005307262]	uncertain significance	5	173151596	173151596	Human		name
598250511	CV3946226	single nucleotide variant	NM_001205.3(BNIP1):c.178-2641C>T	not specified [RCV005298351]	uncertain significance	5	173151681	173151681	Human		name
405763272	CV3291348	single nucleotide variant	NM_001205.3(BNIP1):c.17A>G (p.Asp6Gly)	not specified [RCV004433999]	uncertain significance	5	173144562	173144562	Human		name
597719582	CV3643153	single nucleotide variant	NM_001205.3(BNIP1):c.26T>C (p.Val9Ala)	not specified [RCV004887647]	uncertain significance	5	173144571	173144571	Human		name
598250506	CV3946225	single nucleotide variant	NM_001205.3(BNIP1):c.16G>A (p.Asp6Asn)	not specified [RCV005298350]	uncertain significance	5	173144561	173144561	Human		name
155982338	CV2351589	single nucleotide variant	NM_001205.3(BNIP1):c.41A>C (p.Gln14Pro)	not specified [RCV004195308]	uncertain significance	5	173144586	173144586	Human		name
405763282	CV3291350	single nucleotide variant	NM_001205.3(BNIP1):c.64G>A (p.Glu22Lys)	not specified [RCV004434001]	uncertain significance	5	173144609	173144609	Human		name
597719563	CV3643151	single nucleotide variant	NM_001205.3(BNIP1):c.92G>A (p.Arg31His)	not specified [RCV004887645]	uncertain significance	5	173146873	173146873	Human		name
156179995	CV2324351	single nucleotide variant	NM_001205.3(BNIP1):c.256A>C (p.Lys86Gln)	not specified [RCV004178855]	uncertain significance	5	173154400	173154400	Human		name
156341232	CV2368378	single nucleotide variant	NM_001205.3(BNIP1):c.164G>A (p.Arg55His)	not specified [RCV004219152]	uncertain significance	5	173146945	173146945	Human		name
405763278	CV3291349	single nucleotide variant	NM_001205.3(BNIP1):c.271A>C (p.Asn91His)	not specified [RCV004434000]	uncertain significance	5	173158745	173158745	Human		name
407479734	CV3424050	single nucleotide variant	NM_001205.3(BNIP1):c.173T>C (p.Ile58Thr)	not specified [RCV004602072]	uncertain significance	5	173146954	173146954	Human		name
407500199	CV3424051	single nucleotide variant	NM_001205.3(BNIP1):c.188A>C (p.Gln63Pro)	not specified [RCV004607084]	uncertain significance	5	173154332	173154332	Human		name
597719490	CV3643142	single nucleotide variant	NM_001205.3(BNIP1):c.296A>G (p.Asn99Ser)	not specified [RCV004887637]	uncertain significance	5	173158770	173158770	Human		name
597719536	CV3643148	single nucleotide variant	NM_001205.3(BNIP1):c.240A>C (p.Glu80Asp)	not specified [RCV004887642]	uncertain significance	5	173154384	173154384	Human		name
597719573	CV3643152	single nucleotide variant	NM_001205.3(BNIP1):c.176A>G (p.Gln59Arg)	not specified [RCV004887646]	uncertain significance	5	173146957	173146957	Human		name
598250491	CV3946223	single nucleotide variant	NM_001205.3(BNIP1):c.262A>T (p.Met88Leu)	not specified [RCV005298348]	uncertain significance	5	173154406	173154406	Human		name
156384356	CV2231059	single nucleotide variant	NM_001205.3(BNIP1):c.407G>A (p.Ser136Asn)	not specified [RCV004094290]	uncertain significance	5	173159968	173159968	Human		name
156208728	CV2304342	single nucleotide variant	NM_001205.3(BNIP1):c.559G>A (p.Gly187Ser)	not specified [RCV004164459]	uncertain significance	5	173163793	173163793	Human		name
156347069	CV2315103	single nucleotide variant	NM_001205.3(BNIP1):c.458T>C (p.Val153Ala)	not specified [RCV004165288]	uncertain significance	5	173160019	173160019	Human		name
155977406	CV2321129	single nucleotide variant	NM_001205.3(BNIP1):c.616T>C (p.Phe206Leu)	not specified [RCV004175260]	uncertain significance	5	173163850	173163850	Human		name
156054438	CV2361232	single nucleotide variant	NM_001205.3(BNIP1):c.545G>T (p.Gly182Val)	not specified [RCV004216408]	uncertain significance	5	173163779	173163779	Human		name
155906536	CV2379057	single nucleotide variant	NM_001205.3(BNIP1):c.587G>A (p.Arg196His)	not provided [RCV004696265]\|not specified [RCV004233814]	uncertain significance	5	173163821	173163821	Human		name
405763288	CV3291351	single nucleotide variant	NM_001205.3(BNIP1):c.562C>T (p.Arg188Trp)	not specified [RCV004434002]	uncertain significance	5	173163796	173163796	Human		name
407479721	CV3424048	single nucleotide variant	NM_001205.3(BNIP1):c.563G>A (p.Arg188Gln)	not specified [RCV004602070]	uncertain significance	5	173163797	173163797	Human		name
407479728	CV3424049	single nucleotide variant	NM_001205.3(BNIP1):c.668G>A (p.Arg223Gln)	not specified [RCV004602071]	uncertain significance	5	173163902	173163902	Human		name
597719509	CV3643145	single nucleotide variant	NM_001205.3(BNIP1):c.406A>G (p.Ser136Gly)	not specified [RCV004887639]	uncertain significance	5	173159967	173159967	Human		name
597719518	CV3643146	single nucleotide variant	NM_001205.3(BNIP1):c.348G>C (p.Gln116His)	not specified [RCV004887640]	uncertain significance	5	173158822	173158822	Human		name
597719527	CV3643147	single nucleotide variant	NM_001205.3(BNIP1):c.599C>G (p.Thr200Arg)	not specified [RCV004887641]	uncertain significance	5	173163833	173163833	Human		name
597719554	CV3643150	single nucleotide variant	NM_001205.3(BNIP1):c.316A>G (p.Ile106Val)	not specified [RCV004887644]	uncertain significance	5	173158790	173158790	Human		name
598162626	CV3946222	single nucleotide variant	NM_001205.3(BNIP1):c.469G>A (p.Glu157Lys)	not specified [RCV005307263]	uncertain significance	5	173160030	173160030	Human		name
598250498	CV3946224	single nucleotide variant	NM_001205.3(BNIP1):c.460C>A (p.Gln154Lys)	not specified [RCV005298349]	uncertain significance	5	173160021	173160021	Human		name

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