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29 records found for search term Hspb7
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8629058CV84201single nucleotide variantNM_014424.4(HSPB7):c.-1420G>AMalignant melanoma [RCV000064282]not provided11601938316019383Humanname
405803928CV3270483single nucleotide variantNM_014424.5(HSPB7):c.86C>T (p.Ser29Leu)not specified [RCV004404732]uncertain significance11601787816017878Humanname
598256232CV3968303single nucleotide variantNM_014424.5(HSPB7):c.94C>A (p.Arg32Ser)not specified [RCV005346728]uncertain significance11601787016017870Humanname
15161163CV706778single nucleotide variantNM_014424.5(HSPB7):c.387G>A (p.Pro129=)not provided [RCV000970039]benign11601570616015706Humanname
156284976CV2289024single nucleotide variantNM_014424.5(HSPB7):c.134T>C (p.Leu45Pro)not specified [RCV004149973]uncertain significance11601783016017830Humanname
156281208CV2295096single nucleotide variantNM_014424.5(HSPB7):c.254C>T (p.Ala85Val)not specified [RCV004156200]uncertain significance11601715316017153Humanname
405804021CV3270478single nucleotide variantNM_014424.5(HSPB7):c.101T>C (p.Leu34Pro)not specified [RCV004404727]uncertain significance11601786316017863Humanname
405804019CV3270479single nucleotide variantNM_014424.5(HSPB7):c.116C>T (p.Pro39Leu)not specified [RCV004404728]uncertain significance11601784816017848Humanname
407465428CV3444140single nucleotide variantNM_014424.5(HSPB7):c.149A>C (p.Asp50Ala)not specified [RCV004635253]uncertain significance11601781516017815Humanname
407465318CV3444141single nucleotide variantNM_014424.5(HSPB7):c.212G>A (p.Gly71Glu)not specified [RCV004635254]uncertain significance11601719516017195Humanname
597782791CV3686014single nucleotide variantNM_014424.5(HSPB7):c.262G>A (p.Val88Met)not specified [RCV004931250]uncertain significance11601714516017145Humanname
597782799CV3686016single nucleotide variantNM_014424.5(HSPB7):c.241G>A (p.Ala81Thr)not specified [RCV004931252]uncertain significance11601716616017166Humanname
15161169CV706780single nucleotide variantNM_014424.5(HSPB7):c.152A>G (p.Asp51Gly)not provided [RCV000970040]benign11601781216017812Humanname
15161175CV706781single nucleotide variantNM_014424.5(HSPB7):c.151G>A (p.Asp51Asn)not provided [RCV000970041]benign11601781316017813Humanname
156334150CV2267061single nucleotide variantNM_014424.5(HSPB7):c.325G>A (p.Ala109Thr)not specified [RCV004131694]uncertain significance11601708216017082Humanname
156065496CV2376093single nucleotide variantNM_014424.5(HSPB7):c.493C>T (p.Arg165Trp)not specified [RCV004220328]uncertain significance11601560016015600Humanname
156227316CV2388209single nucleotide variantNM_014424.5(HSPB7):c.368C>T (p.Ala123Val)not specified [RCV004234668]uncertain significance11601572516015725Humanname
156252660CV2390062single nucleotide variantNM_014424.5(HSPB7):c.464C>T (p.Pro155Leu)not specified [RCV004238665]uncertain significance11601562916015629Humanname
11541269CV248544single nucleotide variantNM_014424.5(HSPB7):c.442A>G (p.Thr148Ala)Oromandibular-limb hypogenesis spectrum [RCV000239981]likely benign11601565116015651Human1name
401757425CV2692995single nucleotide variantNM_014424.5(HSPB7):c.448C>T (p.Arg150Trp)not specified [RCV004306504]uncertain significance11601564516015645Humanname
401764507CV2705052single nucleotide variantNM_014424.5(HSPB7):c.364T>C (p.Phe122Leu)not specified [RCV004309968]uncertain significance11601572916015729Humanname
401783674CV2723830single nucleotide variantNM_014424.5(HSPB7):c.322C>T (p.Arg108Trp)not specified [RCV004325975]uncertain significance11601708516017085Humanname
405804017CV3270480single nucleotide variantNM_014424.5(HSPB7):c.352G>A (p.Val118Ile)not specified [RCV004404729]uncertain significance11601574116015741Humanname
405803953CV3270481single nucleotide variantNM_014424.5(HSPB7):c.458G>A (p.Arg153His)not specified [RCV004404730]uncertain significance11601563516015635Humanname
405803926CV3270482single nucleotide variantNM_014424.5(HSPB7):c.494G>A (p.Arg165Gln)not specified [RCV004404731]uncertain significance11601559916015599Humanname
407465201CV3444142single nucleotide variantNM_014424.5(HSPB7):c.425G>C (p.Arg142Pro)not specified [RCV004635255]uncertain significance11601566816015668Humanname
597782796CV3686015single nucleotide variantNM_014424.5(HSPB7):c.496A>C (p.Thr166Pro)not specified [RCV004931251]uncertain significance11601559716015597Humanname
597782804CV3686017single nucleotide variantNM_014424.5(HSPB7):c.418G>A (p.Ala140Thr)not specified [RCV004931253]uncertain significance11601567516015675Humanname
598205835CV3968302single nucleotide variantNM_014424.5(HSPB7):c.316G>A (p.Glu106Lys)not specified [RCV005337670]uncertain significance11601709116017091Humanname