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Variants search result for Homo sapiens
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18 records found for search term Ostf1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8651320CV127895single nucleotide variantNM_012383.4(OSTF1):c.408+875C>TLung cancer [RCV000108382]uncertain significance97513527075135270Humanname
8626734CV81878single nucleotide variantNM_012383.4(OSTF1):c.397C>T (p.Leu133=)Malignant melanoma [RCV000061957]not provided97513438475134384Humanname
156389793CV2380842single nucleotide variantNM_012383.5(OSTF1):c.136G>A (p.Asp46Asn)not specified [RCV004218398]uncertain significance97513058175130581Humanname
401864345CV2781698single nucleotide variantNM_012383.5(OSTF1):c.155G>C (p.Gly52Ala)not specified [RCV004354890]uncertain significance97513060075130600Humanname
405784533CV3374347single nucleotide variantNM_012383.5(OSTF1):c.187A>G (p.Ser63Gly)not specified [RCV004504560]uncertain significance97513063275130632Humanname
407469929CV3459730single nucleotide variantNM_012383.5(OSTF1):c.257T>G (p.Leu86Trp)not specified [RCV004661901]uncertain significance97513330075133300Humanname
597656094CV3567805single nucleotide variantNM_012383.5(OSTF1):c.142A>G (p.Asn48Asp)not specified [RCV004827473]uncertain significance97513058775130587Humanname
597736237CV3567806single nucleotide variantNM_012383.5(OSTF1):c.226C>T (p.Pro76Ser)not specified [RCV004843698]uncertain significance97513179975131799Humanname
156033810CV2211625single nucleotide variantNM_012383.5(OSTF1):c.461A>T (p.Asp154Val)not specified [RCV004084519]uncertain significance97513759075137590Humanname
156172794CV2337627single nucleotide variantNM_012383.5(OSTF1):c.625G>A (p.Asp209Asn)not specified [RCV004181190]uncertain significance97514672175146721Humanname
156342639CV2344028single nucleotide variantNM_012383.5(OSTF1):c.625G>T (p.Asp209Tyr)not specified [RCV004195639]uncertain significance97514672175146721Humanname
156037192CV2374048single nucleotide variantNM_012383.5(OSTF1):c.506G>C (p.Arg169Thr)not specified [RCV004227171]uncertain significance97514085275140852Humanname
401777116CV2721612single nucleotide variantNM_012383.5(OSTF1):c.488G>A (p.Gly163Asp)not specified [RCV004316116]uncertain significance97514083475140834Humanname
405784539CV3374348single nucleotide variantNM_012383.5(OSTF1):c.545A>G (p.Asn182Ser)not specified [RCV004504561]uncertain significance97514089175140891Humanname
407511428CV3459727single nucleotide variantNM_012383.5(OSTF1):c.364G>C (p.Val122Leu)not specified [RCV004648044]uncertain significance97513435175134351Humanname
407511431CV3459728single nucleotide variantNM_012383.5(OSTF1):c.629A>G (p.Asp210Gly)not specified [RCV004648045]uncertain significance97514672575146725Humanname
407469924CV3459729single nucleotide variantNM_012383.5(OSTF1):c.356A>G (p.Lys119Arg)not specified [RCV004661900]uncertain significance97513339975133399Humanname
597736232CV3567804single nucleotide variantNM_012383.5(OSTF1):c.302G>T (p.Gly101Val)not specified [RCV004843697]uncertain significance97513334575133345Humanname