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Variants search result for Homo sapiens
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35 records found for search term Bag1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156126012CV2283674single nucleotide variantNM_004323.6(BAG1):c.14G>T (p.Gly5Val)not specified [RCV004142210]uncertain significance93326466133264661Humanname
155985909CV2343983single nucleotide variantNM_004323.6(BAG1):c.46C>T (p.Arg16Trp)not specified [RCV004195600]uncertain significance93326462933264629Humanname
156094425CV2377727single nucleotide variantNM_004323.6(BAG1):c.73C>T (p.Arg25Trp)not specified [RCV004230315]uncertain significance93326460233264602Humanname
407487617CV3420981single nucleotide variantNM_004323.6(BAG1):c.47G>T (p.Arg16Leu)not specified [RCV004603802]uncertain significance93326462833264628Humanname
155934517CV2225319single nucleotide variantNM_004323.6(BAG1):c.134G>T (p.Gly45Val)not specified [RCV004098956]uncertain significance93326454133264541Humanname
155945829CV2265874single nucleotide variantNM_004323.6(BAG1):c.146C>G (p.Ala49Gly)not specified [RCV004126734]uncertain significance93326452933264529Humanname
156258749CV2395414single nucleotide variantNM_004323.6(BAG1):c.244C>T (p.Arg82Trp)not specified [RCV004241289]uncertain significance93326443133264431Humanname
329374275CV2443812single nucleotide variantNM_004323.6(BAG1):c.131C>T (p.Ser44Phe)not specified [RCV004258152]uncertain significance93326454433264544Humanname
329389245CV2448826single nucleotide variantNM_004323.6(BAG1):c.146C>T (p.Ala49Val)not specified [RCV004261513]likely benign93326452933264529Humanname
401735440CV2699269single nucleotide variantNM_004323.6(BAG1):c.194C>T (p.Ala65Val)not specified [RCV004305537]uncertain significance93326448133264481Humanname
405691257CV3290793single nucleotide variantNM_004323.6(BAG1):c.190G>A (p.Ala64Thr)not specified [RCV004423706]uncertain significance93326448533264485Humanname
407487552CV3420970single nucleotide variantNM_004323.6(BAG1):c.209C>G (p.Pro70Arg)not specified [RCV004603791]uncertain significance93326446633264466Humanname
597741208CV3631319single nucleotide variantNM_004323.6(BAG1):c.176C>T (p.Pro59Leu)not specified [RCV004890707]uncertain significance93326449933264499Humanname
597741305CV3631337single nucleotide variantNM_004323.6(BAG1):c.220A>G (p.Lys74Glu)not specified [RCV004890725]uncertain significance93326445533264455Humanname
598268782CV3926399single nucleotide variantNM_004323.6(BAG1):c.170A>C (p.Asp57Ala)not specified [RCV005302446]uncertain significance93326450533264505Humanname
598235034CV3926431single nucleotide variantNM_004323.6(BAG1):c.160A>G (p.Ser54Gly)not specified [RCV005295795]uncertain significance93326451533264515Humanname
156069256CV2237117single nucleotide variantNM_004323.6(BAG1):c.328G>A (p.Ala110Thr)not specified [RCV004114870]uncertain significance93326434733264347Humanname
156341091CV2268218single nucleotide variantNM_004323.6(BAG1):c.547G>A (p.Val183Ile)not specified [RCV004138523]uncertain significance93326273533262735Humanname
155927927CV2280969single nucleotide variantNM_004323.6(BAG1):c.612G>C (p.Leu204Phe)not specified [RCV004145474]uncertain significance93326113833261138Humanname
156401879CV2371088single nucleotide variantNM_004323.6(BAG1):c.950C>T (p.Ala317Val)not specified [RCV004220841]uncertain significance93325530733255307Humanname
156137380CV2375746single nucleotide variantNM_004323.6(BAG1):c.641G>A (p.Arg214Gln)not specified [RCV004224341]uncertain significance93326110933261109Humanname
401740544CV2702392single nucleotide variantNM_004323.6(BAG1):c.656G>A (p.Gly219Glu)not specified [RCV004316915]uncertain significance93326109433261094Humanname
401742548CV2715257single nucleotide variantNM_004323.6(BAG1):c.899A>G (p.Asn300Ser)not specified [RCV004324601]uncertain significance93325591433255914Humanname
401864536CV2760946single nucleotide variantNM_004323.6(BAG1):c.961G>A (p.Glu321Lys)not specified [RCV004336578]uncertain significance93325529633255296Humanname
405691263CV3290794single nucleotide variantNM_004323.6(BAG1):c.346A>G (p.Met116Val)not specified [RCV004423707]likely benign93326432933264329Humanname
405691270CV3290795single nucleotide variantNM_004323.6(BAG1):c.391A>G (p.Ser131Gly)not specified [RCV004423708]uncertain significance93326428433264284Humanname
405691276CV3290796single nucleotide variantNM_004323.6(BAG1):c.411G>T (p.Glu137Asp)not specified [RCV004423709]uncertain significance93326426433264264Humanname
405691282CV3290797single nucleotide variantNM_004323.6(BAG1):c.536A>G (p.Glu179Gly)not specified [RCV004423710]uncertain significance93326274633262746Humanname
405691294CV3290799single nucleotide variantNM_004323.6(BAG1):c.598A>G (p.Met200Val)not specified [RCV004423712]uncertain significance93326115233261152Humanname
405691300CV3290800single nucleotide variantNM_004323.6(BAG1):c.682G>A (p.Val228Ile)not specified [RCV004423713]uncertain significance93325901533259015Humanname
407487500CV3420959single nucleotide variantNM_004323.6(BAG1):c.714G>C (p.Lys238Asn)not specified [RCV004603781]uncertain significance93325898333258983Humanname
597705631CV3631310single nucleotide variantNM_004323.6(BAG1):c.608C>T (p.Pro203Leu)not specified [RCV004886159]uncertain significance93326114233261142Humanname
597741266CV3631330single nucleotide variantNM_004323.6(BAG1):c.809C>T (p.Ala270Val)not specified [RCV004890718]uncertain significance93325687733256877Humanname
598268850CV3926421single nucleotide variantNM_004323.6(BAG1):c.838G>A (p.Ala280Thr)not specified [RCV005302459]uncertain significance93325684833256848Humanname
15146186CV711950single nucleotide variantNM_004323.6(BAG1):c.910A>G (p.Ser304Gly)not provided [RCV000967123]benign93325590333255903Humanname