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Variants search result for Homo sapiens
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22 records found for search term Pih1d2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597740538CV3579656single nucleotide variantNM_138789.4(PIH1D2):c.23T>C (p.Leu8Pro)not specified [RCV004844466]uncertain significance11112073152112073152Humanname
156128376CV2238448single nucleotide variantNM_138789.4(PIH1D2):c.73A>C (p.Ser25Arg)not specified [RCV004113506]uncertain significance11112073102112073102Humanname
405780063CV3372518single nucleotide variantNM_138789.4(PIH1D2):c.244A>G (p.Thr82Ala)not specified [RCV004503787]likely benign11112071692112071692Humanname
598197844CV4006559single nucleotide variantNM_138789.4(PIH1D2):c.250C>T (p.His84Tyr)not specified [RCV005397931]uncertain significance11112071686112071686Humanname
598197852CV4006560single nucleotide variantNM_138789.4(PIH1D2):c.129G>T (p.Gln43His)not specified [RCV005397932]uncertain significance11112073046112073046Humanname
156035251CV2253026single nucleotide variantNM_138789.4(PIH1D2):c.712A>C (p.Lys238Gln)not specified [RCV004120821]uncertain significance11112070537112070537Humanname
156242934CV2283229single nucleotide variantNM_138789.4(PIH1D2):c.690G>A (p.Met230Ile)not specified [RCV004145901]likely benign11112070559112070559Humanname
156195982CV2306682single nucleotide variantNM_138789.4(PIH1D2):c.611T>C (p.Leu204Ser)not specified [RCV004159276]uncertain significance11112070638112070638Humanname
155921312CV2340430single nucleotide variantNM_138789.4(PIH1D2):c.593A>G (p.Asp198Gly)not specified [RCV004197158]uncertain significance11112070656112070656Humanname
156080651CV2384669single nucleotide variantNM_138789.4(PIH1D2):c.635G>C (p.Gly212Ala)not specified [RCV004232445]uncertain significance11112070614112070614Humanname
156188895CV2395551single nucleotide variantNM_138789.4(PIH1D2):c.641C>T (p.Ala214Val)not specified [RCV004241405]uncertain significance11112070608112070608Humanname
329383256CV2434482single nucleotide variantNM_138789.4(PIH1D2):c.473G>C (p.Ser158Thr)not specified [RCV004254191]uncertain significance11112071112112071112Humanname
405780068CV3372519single nucleotide variantNM_138789.4(PIH1D2):c.427A>T (p.Thr143Ser)not specified [RCV004503788]uncertain significance11112071158112071158Humanname
405780074CV3372520single nucleotide variantNM_138789.4(PIH1D2):c.472A>C (p.Ser158Arg)not specified [RCV004503789]uncertain significance11112071113112071113Humanname
405780086CV3372522single nucleotide variantNM_138789.4(PIH1D2):c.839A>T (p.Glu280Val)not specified [RCV004503791]uncertain significance11112067980112067980Humanname
407530681CV3463526single nucleotide variantNM_138789.4(PIH1D2):c.841A>C (p.Lys281Gln)not specified [RCV004657186]uncertain significance11112067978112067978Humanname
597767301CV3579653single nucleotide variantNM_138789.4(PIH1D2):c.860A>G (p.Asn287Ser)not specified [RCV004850439]uncertain significance11112067959112067959Humanname
597740543CV3579654single nucleotide variantNM_138789.4(PIH1D2):c.920C>T (p.Thr307Met)not specified [RCV004844465]uncertain significance11112067899112067899Humanname
597767306CV3579655single nucleotide variantNM_138789.4(PIH1D2):c.811G>A (p.Glu271Lys)not specified [RCV004850440]uncertain significance11112070438112070438Humanname
597740535CV3579657single nucleotide variantNM_138789.4(PIH1D2):c.338A>G (p.Asp113Gly)not specified [RCV004844467]uncertain significance11112071247112071247Humanname
598272288CV4006561single nucleotide variantNM_138789.4(PIH1D2):c.321T>A (p.Asp107Glu)not specified [RCV005389351]uncertain significance11112071264112071264Humanname
155924957CV2358242single nucleotide variantNM_001082619.2(PIH1D2):c.839C>T (p.Ala280Val)not specified [RCV004212033]uncertain significance11112064196112064196Humanname