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Variants search result for Homo sapiens
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42 records found for search term Cap1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15184840CV696735single nucleotide variantNM_006367.4(CAP1):c.93T>C (p.Tyr31=)not provided [RCV000952806]benign14005943940059439Humanname
401772557CV2712794single nucleotide variantNM_006367.4(CAP1):c.22G>A (p.Val8Ile)not specified [RCV004314223]uncertain significance14005936840059368Humanname
15194639CV696736single nucleotide variantNM_006367.4(CAP1):c.219G>A (p.Ala73=)not provided [RCV000955701]benign14006173740061737Humanname
155955367CV2274448single nucleotide variantNM_006367.4(CAP1):c.85C>T (p.Arg29Cys)not specified [RCV004136812]likely benign14005943140059431Humanname
405768363CV3298831single nucleotide variantNM_006367.4(CAP1):c.86G>A (p.Arg29His)not specified [RCV004434846]uncertain significance14005943240059432Humanname
597750883CV3647638single nucleotide variantNM_006367.4(CAP1):c.73T>C (p.Ser25Pro)not specified [RCV004892650]uncertain significance14005941940059419Humanname
598204641CV3943107single nucleotide variantNM_006367.4(CAP1):c.61G>A (p.Val21Ile)not specified [RCV005314827]uncertain significance14005940740059407Humanname
156276886CV2209823single nucleotide variantNM_006367.4(CAP1):c.104C>T (p.Pro35Leu)not specified [RCV004076287]uncertain significance14005945040059450Humanname
405768333CV3298826single nucleotide variantNM_006367.4(CAP1):c.254C>T (p.Ala85Val)not specified [RCV004434841]uncertain significance14006177240061772Humanname
407501139CV3424590single nucleotide variantNM_006367.4(CAP1):c.155C>T (p.Ala52Val)not specified [RCV004607308]uncertain significance14006010940060109Humanname
598204636CV3943106single nucleotide variantNM_006367.4(CAP1):c.176T>C (p.Leu59Ser)not specified [RCV005314826]uncertain significance14006013040060130Humanname
598204653CV3943109single nucleotide variantNM_006367.4(CAP1):c.107C>T (p.Ser36Leu)not specified [RCV005314829]uncertain significance14005945340059453Humanname
156064859CV2317724single nucleotide variantNM_006367.4(CAP1):c.433G>T (p.Ala145Ser)not specified [RCV004174985]uncertain significance14006436540064365Humanname
156181864CV2384112single nucleotide variantNM_006367.4(CAP1):c.370G>A (p.Gly124Ser)not specified [RCV004227517]uncertain significance14006430240064302Humanname
329390556CV2455291single nucleotide variantNM_006367.4(CAP1):c.514T>C (p.Tyr172His)not specified [RCV004274801]uncertain significance14006454940064549Humanname
401780908CV2681815single nucleotide variantNM_006367.4(CAP1):c.775G>A (p.Ala259Thr)not specified [RCV004296817]uncertain significance14006768440067684Humanname
401775424CV2724093single nucleotide variantNM_006367.4(CAP1):c.722C>T (p.Pro241Leu)not specified [RCV004326232]uncertain significance14006763140067631Humanname
401890383CV2768165single nucleotide variantNM_006367.4(CAP1):c.485T>C (p.Met162Thr)not specified [RCV004350176]uncertain significance14006452040064520Humanname
401879534CV2769643single nucleotide variantNM_006367.4(CAP1):c.929C>T (p.Ser310Phe)not specified [RCV004351573]uncertain significance14006981040069810Humanname
405768339CV3298827single nucleotide variantNM_006367.4(CAP1):c.343G>T (p.Val115Leu)not specified [RCV004434842]uncertain significance14006427540064275Humanname
405768351CV3298829single nucleotide variantNM_006367.4(CAP1):c.761G>A (p.Arg254His)not specified [RCV004434844]uncertain significance14006767040067670Humanname
405768357CV3298830single nucleotide variantNM_006367.4(CAP1):c.798C>G (p.Ser266Arg)not specified [RCV004434845]uncertain significance14006770740067707Humanname
405768369CV3298832single nucleotide variantNM_006367.4(CAP1):c.905C>T (p.Ala302Val)not specified [RCV004434847]uncertain significance14006978640069786Humanname
405768374CV3298833single nucleotide variantNM_006367.4(CAP1):c.938G>A (p.Arg313Gln)not specified [RCV004434848]uncertain significance14006981940069819Humanname
405768380CV3298834single nucleotide variantNM_006367.4(CAP1):c.964C>T (p.Leu322Phe)not specified [RCV004434849]uncertain significance14006984540069845Humanname
407474902CV3424591single nucleotide variantNM_006367.4(CAP1):c.355C>T (p.Arg119Trp)not specified [RCV004600741]uncertain significance14006428740064287Humanname
597750872CV3647632single nucleotide variantNM_006367.4(CAP1):c.679G>A (p.Gly227Arg)not specified [RCV004892648]uncertain significance14006758840067588Humanname
597764496CV3647633single nucleotide variantNM_006367.4(CAP1):c.775G>T (p.Ala259Ser)not specified [RCV004895637]uncertain significance14006768440067684Humanname
597750877CV3647635single nucleotide variantNM_006367.4(CAP1):c.872G>A (p.Gly291Asp)not specified [RCV004892649]uncertain significance14006975340069753Humanname
597764504CV3647636single nucleotide variantNM_006367.4(CAP1):c.326C>T (p.Ser109Leu)not specified [RCV004895639]uncertain significance14006425840064258Humanname
597764507CV3647637single nucleotide variantNM_006367.4(CAP1):c.833T>C (p.Met278Thr)not specified [RCV004895640]uncertain significance14006971440069714Humanname
597764511CV3647639single nucleotide variantNM_006367.4(CAP1):c.662C>T (p.Pro221Leu)not specified [RCV004895641]uncertain significance14006757140067571Humanname
598204630CV3943105single nucleotide variantNM_006367.4(CAP1):c.312G>T (p.Leu104Phe)not specified [RCV005314825]uncertain significance14006424440064244Humanname
598204647CV3943108single nucleotide variantNM_006367.4(CAP1):c.878T>C (p.Val293Ala)not specified [RCV005314828]uncertain significance14006975940069759Humanname
598204659CV3943110single nucleotide variantNM_006367.4(CAP1):c.671C>T (p.Pro224Leu)not specified [RCV005314830]uncertain significance14006758040067580Humanname
598212806CV3943111single nucleotide variantNM_006367.4(CAP1):c.561A>C (p.Leu187Phe)not specified [RCV005316221]uncertain significance14006625140066251Humanname
598204665CV3943112single nucleotide variantNM_006367.4(CAP1):c.944C>T (p.Thr315Ile)not specified [RCV005314831]uncertain significance14006982540069825Humanname
156204143CV2331619single nucleotide variantNM_006367.4(CAP1):c.1108A>G (p.Ile370Val)not specified [RCV004184254]uncertain significance14007027340070273Humanname
405768323CV3298824single nucleotide variantNM_006367.4(CAP1):c.1069G>A (p.Val357Ile)not specified [RCV004434839]uncertain significance14007023440070234Humanname
405768329CV3298825single nucleotide variantNM_006367.4(CAP1):c.1078A>G (p.Thr360Ala)not specified [RCV004434840]uncertain significance14007024340070243Humanname
597764490CV3647631single nucleotide variantNM_006367.4(CAP1):c.1059A>G (p.Ile353Met)not specified [RCV004895636]uncertain significance14007022440070224Humanname
597764500CV3647634single nucleotide variantNM_006367.4(CAP1):c.1132C>T (p.Leu378Phe)not specified [RCV004895638]uncertain significance14007044440070444Humanname