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22 records found for search term Gpr65
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597769781CV3681601single nucleotide variantNM_003608.4(GPR65):c.13T>C (p.Cys5Arg)not specified [RCV004928143]uncertain significance148801086088010860Humanname
598274656CV3967371single nucleotide variantNM_003608.4(GPR65):c.26A>G (p.Gln9Arg)not specified [RCV005351523]uncertain significance148801087388010873Humanname
156165705CV2373523single nucleotide variantNM_003608.4(GPR65):c.87T>G (p.Ile29Met)not specified [RCV004222633]uncertain significance148801093488010934Humanname
156209862CV2304608single nucleotide variantNM_003608.4(GPR65):c.116C>T (p.Ser39Phe)not specified [RCV004166499]uncertain significance148801096388010963Humanname
407526717CV3436787single nucleotide variantNM_003608.4(GPR65):c.187T>G (p.Tyr63Asp)not specified [RCV004632535]uncertain significance148801103488011034Humanname
597769777CV3681600single nucleotide variantNM_003608.4(GPR65):c.286A>G (p.Met96Val)not specified [RCV004928142]uncertain significance148801113388011133Humanname
597769786CV3681602single nucleotide variantNM_003608.4(GPR65):c.107T>C (p.Leu36Pro)not specified [RCV004928144]uncertain significance148801095488010954Humanname
598274648CV3967367single nucleotide variantNM_003608.4(GPR65):c.211A>G (p.Ile71Val)not specified [RCV005351519]uncertain significance148801105888011058Humanname
8635313CV90535single nucleotide variantNM_003608.3(GPR65):c.202C>T (p.Pro68Ser)Malignant melanoma [RCV000070633]not provided148801104988011049Humanname
155994454CV2277975single nucleotide variantNM_003608.4(GPR65):c.580A>G (p.Ile194Val)not specified [RCV004141219]likely benign148801142788011427Humanname
156179259CV2298364single nucleotide variantNM_003608.4(GPR65):c.496A>T (p.Asn166Tyr)not specified [RCV004160257]uncertain significance148801134388011343Humanname
156094894CV2310051single nucleotide variantNM_003608.4(GPR65):c.325G>A (p.Ala109Thr)not specified [RCV004163184]uncertain significance148801117288011172Humanname
156050819CV2336619single nucleotide variantNM_003608.4(GPR65):c.466G>A (p.Val156Ile)not specified [RCV004196864]uncertain significance148801131388011313Humanname
156074170CV2376953single nucleotide variantNM_003608.4(GPR65):c.902T>C (p.Met301Thr)not specified [RCV004229641]uncertain significance148801174988011749Humanname
401746298CV2695541single nucleotide variantNM_003608.4(GPR65):c.404G>A (p.Ser135Asn)not specified [RCV004305716]uncertain significance148801125188011251Humanname
405739766CV3252073single nucleotide variantNM_003608.4(GPR65):c.644C>T (p.Ala215Val)not specified [RCV004391157]uncertain significance148801149188011491Humanname
405739771CV3252074single nucleotide variantNM_003608.4(GPR65):c.800G>A (p.Arg267Gln)not specified [RCV004391158]likely benign148801164788011647Humanname
407526714CV3436786single nucleotide variantNM_003608.4(GPR65):c.386G>C (p.Arg129Thr)not specified [RCV004632534]uncertain significance148801123388011233Humanname
597769791CV3681603single nucleotide variantNM_003608.4(GPR65):c.960A>T (p.Lys320Asn)not specified [RCV004928145]uncertain significance148801180788011807Humanname
598274650CV3967368single nucleotide variantNM_003608.4(GPR65):c.488A>T (p.Glu163Val)not specified [RCV005351520]uncertain significance148801133588011335Humanname
598274652CV3967369single nucleotide variantNM_003608.4(GPR65):c.656A>G (p.Lys219Arg)not specified [RCV005351521]uncertain significance148801150388011503Humanname
8635314CV90536single nucleotide variantNM_003608.3(GPR65):c.611G>A (p.Arg204Gln)Malignant melanoma [RCV000070634]not provided148801145888011458Humanname