Sstr1 Variant Search Result - Rat Genome Database

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34 records found for search term Sstr1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15189170	CV739206	single nucleotide variant	NM_001049.3(SSTR1):c.243C>T (p.Tyr81=)	not provided [RCV000909574]	likely benign	14	38209632	38209632	Human		name
329360750	CV2462933	single nucleotide variant	NM_001049.3(SSTR1):c.98G>C (p.Gly33Ala)	not specified [RCV004272770]	uncertain significance	14	38209487	38209487	Human		name
407517412	CV3474994	single nucleotide variant	NM_001049.3(SSTR1):c.56G>A (p.Gly19Asp)	not specified [RCV004675514]	uncertain significance	14	38209445	38209445	Human		name
407517407	CV3474997	single nucleotide variant	NM_001049.3(SSTR1):c.70G>C (p.Gly24Arg)	not specified [RCV004675516]	uncertain significance	14	38209459	38209459	Human		name
597682270	CV3608448	single nucleotide variant	NM_001049.3(SSTR1):c.86G>A (p.Gly29Asp)	not specified [RCV004857563]	uncertain significance	14	38209475	38209475	Human		name
597779864	CV3608451	single nucleotide variant	NM_001049.3(SSTR1):c.43A>G (p.Ser15Gly)	not specified [RCV004873682]	uncertain significance	14	38209432	38209432	Human		name
597779876	CV3608455	single nucleotide variant	NM_001049.3(SSTR1):c.61T>G (p.Cys21Gly)	not specified [RCV004873685]	uncertain significance	14	38209450	38209450	Human		name
15161014	CV714120	single nucleotide variant	NM_001049.3(SSTR1):c.408G>A (p.Val136=)	not provided [RCV000970012]	benign	14	38209797	38209797	Human		name
405719329	CV3327147	single nucleotide variant	NM_001049.3(SSTR1):c.244G>T (p.Val82Leu)	not specified [RCV004462910]	uncertain significance	14	38209633	38209633	Human		name
405719335	CV3327148	single nucleotide variant	NM_001049.3(SSTR1):c.256T>C (p.Tyr86His)	not specified [RCV004462911]	uncertain significance	14	38209645	38209645	Human		name
407517404	CV3474998	single nucleotide variant	NM_001049.3(SSTR1):c.253C>T (p.Arg85Cys)	not specified [RCV004675517]	uncertain significance	14	38209642	38209642	Human		name
597779872	CV3608454	single nucleotide variant	NM_001049.3(SSTR1):c.189C>A (p.Phe63Leu)	not specified [RCV004873684]	uncertain significance	14	38209578	38209578	Human		name
156210036	CV2304629	single nucleotide variant	NM_001049.3(SSTR1):c.976C>G (p.Leu326Val)	not specified [RCV004166519]	uncertain significance	14	38210365	38210365	Human		name
156196881	CV2357502	single nucleotide variant	NM_001049.3(SSTR1):c.457G>T (p.Val153Leu)	not specified [RCV004202782]	uncertain significance	14	38209846	38209846	Human		name
329352462	CV2453050	single nucleotide variant	NM_001049.3(SSTR1):c.688A>G (p.Met230Val)	not specified [RCV004277663]	uncertain significance	14	38210077	38210077	Human		name
329382779	CV2465370	single nucleotide variant	NM_001049.3(SSTR1):c.689T>G (p.Met230Arg)	not specified [RCV004281151]	uncertain significance	14	38210078	38210078	Human		name
401723773	CV2684862	single nucleotide variant	NM_001049.3(SSTR1):c.974T>G (p.Phe325Cys)	not specified [RCV004296368]	uncertain significance	14	38210363	38210363	Human		name
405719344	CV3327149	single nucleotide variant	NM_001049.3(SSTR1):c.452T>C (p.Leu151Pro)	not specified [RCV004462912]	uncertain significance	14	38209841	38209841	Human		name
405719351	CV3327150	single nucleotide variant	NM_001049.3(SSTR1):c.890C>T (p.Ala297Val)	not specified [RCV004462913]	uncertain significance	14	38210279	38210279	Human		name
407517415	CV3474993	single nucleotide variant	NM_001049.3(SSTR1):c.763C>G (p.Leu255Val)	not specified [RCV004675513]	uncertain significance	14	38210152	38210152	Human		name
407526120	CV3474995	single nucleotide variant	NM_001049.3(SSTR1):c.568C>A (p.Leu190Met)	not specified [RCV004679538]	uncertain significance	14	38209957	38209957	Human		name
407517410	CV3474996	single nucleotide variant	NM_001049.3(SSTR1):c.491A>G (p.Lys164Arg)	not specified [RCV004675515]	uncertain significance	14	38209880	38209880	Human		name
597682251	CV3608450	single nucleotide variant	NM_001049.3(SSTR1):c.738C>G (p.Ile246Met)	not specified [RCV004857565]	uncertain significance	14	38210127	38210127	Human		name
597682233	CV3608456	single nucleotide variant	NM_001049.3(SSTR1):c.855G>T (p.Met285Ile)	not specified [RCV004857567]	uncertain significance	14	38210244	38210244	Human		name
598214045	CV3922993	single nucleotide variant	NM_001049.3(SSTR1):c.541G>C (p.Val181Leu)	not specified [RCV005271059]	uncertain significance	14	38209930	38209930	Human		name
155923452	CV2215651	single nucleotide variant	NM_001049.3(SSTR1):c.1052T>C (p.Val351Ala)	not specified [RCV004089397]	uncertain significance	14	38210441	38210441	Human		name
156014607	CV2301514	single nucleotide variant	NM_001049.3(SSTR1):c.1139G>C (p.Arg380Pro)	not specified [RCV004162432]	uncertain significance	14	38210528	38210528	Human		name
407517401	CV3474999	single nucleotide variant	NM_001049.3(SSTR1):c.1118T>G (p.Leu373Arg)	not specified [RCV004675518]	uncertain significance	14	38210507	38210507	Human		name
597682278	CV3608447	single nucleotide variant	NM_001049.3(SSTR1):c.1091G>A (p.Ser364Asn)	not specified [RCV004857562]	uncertain significance	14	38210480	38210480	Human		name
597682260	CV3608449	single nucleotide variant	NM_001049.3(SSTR1):c.1159C>G (p.Arg387Gly)	not specified [RCV004857564]	uncertain significance	14	38210548	38210548	Human		name
597779868	CV3608452	single nucleotide variant	NM_001049.3(SSTR1):c.1126G>C (p.Gly376Arg)	not specified [RCV004873683]	uncertain significance	14	38210515	38210515	Human		name
597682242	CV3608453	single nucleotide variant	NM_001049.3(SSTR1):c.1126G>A (p.Gly376Ser)	not specified [RCV004857566]	uncertain significance	14	38210515	38210515	Human		name
598214052	CV3922992	single nucleotide variant	NM_001049.3(SSTR1):c.1034A>G (p.Asn345Ser)	not specified [RCV005271058]	uncertain significance	14	38210423	38210423	Human		name
598174980	CV3922994	single nucleotide variant	NM_001049.3(SSTR1):c.1006C>A (p.Arg336Ser)	not specified [RCV005285424]	uncertain significance	14	38210395	38210395	Human		name

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