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18 records found for search term Drap1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15161111CV724615single nucleotide variantNM_006442.4(DRAP1):c.48G>A (p.Arg16=)not provided [RCV000881511]benign116591978565919785Humanname
597734720CV3663777single nucleotide variantNM_006442.4(DRAP1):c.10A>C (p.Lys4Gln)not specified [RCV004920323]uncertain significance116591951165919511Humanname
597681183CV3663779single nucleotide variantNM_006442.4(DRAP1):c.130C>T (p.Leu44Phe)not specified [RCV004914312]uncertain significance116591996265919962Humanname
156166007CV2200869single nucleotide variantNM_006442.4(DRAP1):c.390C>G (p.Asp130Glu)not specified [RCV004081495]uncertain significance116592062965920629Humanname
155915047CV2203949single nucleotide variantNM_006442.4(DRAP1):c.446C>G (p.Thr149Ser)not specified [RCV004069995]uncertain significance116592090665920906Humanname
156069161CV2232157single nucleotide variantNM_006442.4(DRAP1):c.371T>C (p.Met124Thr)not specified [RCV004104964]uncertain significance116592061065920610Humanname
155957935CV2304225single nucleotide variantNM_006442.4(DRAP1):c.530T>C (p.Leu177Pro)not specified [RCV004170245]uncertain significance116592134765921347Humanname
156282165CV2338517single nucleotide variantNM_006442.4(DRAP1):c.569C>T (p.Pro190Leu)not specified [RCV004188555]uncertain significance116592138665921386Humanname
155915889CV2339227single nucleotide variantNM_006442.4(DRAP1):c.551C>T (p.Pro184Leu)not specified [RCV004191468]uncertain significance116592136865921368Humanname
329373414CV2434241single nucleotide variantNM_006442.4(DRAP1):c.325C>T (p.Arg109Cys)not specified [RCV004251917]uncertain significance116592045865920458Humanname
405713521CV3248075single nucleotide variantNM_006442.4(DRAP1):c.332G>A (p.Gly111Asp)not specified [RCV004377030]uncertain significance116592057165920571Humanname
405713529CV3248076single nucleotide variantNM_006442.4(DRAP1):c.520A>C (p.Thr174Pro)not specified [RCV004377031]uncertain significance116592133765921337Humanname
405713544CV3248078single nucleotide variantNM_006442.4(DRAP1):c.586G>A (p.Asp196Asn)not specified [RCV004377033]uncertain significance116592140365921403Humanname
407488937CV3434675single nucleotide variantNM_006442.4(DRAP1):c.555G>T (p.Leu185Phe)not specified [RCV004619826]uncertain significance116592137265921372Humanname
407488942CV3434676single nucleotide variantNM_006442.4(DRAP1):c.334C>T (p.Arg112Trp)not specified [RCV004619827]uncertain significance116592057365920573Humanname
597681168CV3663776single nucleotide variantNM_006442.4(DRAP1):c.594G>C (p.Glu198Asp)not specified [RCV004914310]uncertain significance116592141165921411Humanname
597681174CV3663778single nucleotide variantNM_006442.4(DRAP1):c.538G>A (p.Ala180Thr)not specified [RCV004914311]likely benign116592135565921355Humanname
597681191CV3663780single nucleotide variantNM_006442.4(DRAP1):c.515C>T (p.Pro172Leu)not specified [RCV004914313]uncertain significance116592133265921332Humanname