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Variants search result for Homo sapiens
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32 records found for search term Necap2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156278668CV2348247single nucleotide variantNM_018090.5(NECAP2):c.*9C>Tnot specified [RCV004191287]uncertain significance11645889916458899Humanname
597670155CV3555789single nucleotide variantNM_018090.5(NECAP2):c.*1C>Anot specified [RCV004829647]uncertain significance11645889116458891Humanname
405807635CV3356521single nucleotide variantNM_018090.5(NECAP2):c.*44C>Tnot specified [RCV004480781]uncertain significance11645893416458934Humanname
405807648CV3356528single nucleotide variantNM_018090.5(NECAP2):c.*63A>Gnot specified [RCV004480788]uncertain significance11645895316458953Humanname
597670115CV3555784single nucleotide variantNM_018090.5(NECAP2):c.*39C>Tnot specified [RCV004829642]uncertain significance11645892916458929Humanname
597670124CV3555785single nucleotide variantNM_018090.5(NECAP2):c.*66A>Tnot specified [RCV004829643]uncertain significance11645895616458956Humanname
15176791CV706826single nucleotide variantNM_018090.5(NECAP2):c.30C>G (p.Leu10=)not provided [RCV000973269]benign11644079116440791Humanname
155970033CV2309142single nucleotide variantNM_018090.5(NECAP2):c.13G>C (p.Gly5Arg)not specified [RCV004171496]uncertain significance11644077416440774Humanname
156110486CV2387649single nucleotide variantNM_018090.5(NECAP2):c.50A>G (p.His17Arg)not specified [RCV004234197]uncertain significance11644081116440811Humanname
401860368CV2768568single nucleotide variantNM_018090.5(NECAP2):c.50A>T (p.His17Leu)not specified [RCV004344433]uncertain significance11644081116440811Humanname
405807629CV3356518single nucleotide variantNM_018090.5(NECAP2):c.68C>T (p.Pro23Leu)not specified [RCV004480778]uncertain significance11644082916440829Humanname
598254123CV3990607single nucleotide variantNM_018090.5(NECAP2):c.38A>G (p.Lys13Arg)not specified [RCV005385457]uncertain significance11644079916440799Humanname
156034211CV2211734single nucleotide variantNM_018090.5(NECAP2):c.134G>A (p.Arg45Gln)not specified [RCV004084615]uncertain significance11644367316443673Humanname
156380044CV2218033single nucleotide variantNM_018090.5(NECAP2):c.217G>A (p.Val73Met)not specified [RCV004086474]uncertain significance11644789316447893Humanname
156230778CV2348707single nucleotide variantNM_018090.5(NECAP2):c.215C>T (p.Pro72Leu)not specified [RCV004201119]uncertain significance11644789116447891Humanname
401732687CV2685303single nucleotide variantNM_018090.5(NECAP2):c.254C>T (p.Thr85Met)not specified [RCV004292302]uncertain significance11644793016447930Humanname
407489397CV3454785single nucleotide variantNM_018090.5(NECAP2):c.133C>T (p.Arg45Trp)not specified [RCV004641460]uncertain significance11644367216443672Humanname
9686851CV171305single nucleotide variantNM_018090.5(NECAP2):c.462G>T (p.Glu154Asp)Prostate cancer [RCV000149069]uncertain significance11644917416449174Human2name
156032319CV2275008single nucleotide variantNM_018090.5(NECAP2):c.786G>C (p.Gln262His)not specified [RCV004135050]uncertain significance11645888416458884Humanname
155905375CV2303095single nucleotide variantNM_018090.5(NECAP2):c.305G>A (p.Arg102Gln)not specified [RCV004156876]uncertain significance11644806616448066Humanname
405807602CV3356504single nucleotide variantNM_018090.5(NECAP2):c.563T>C (p.Leu188Pro)not specified [RCV004480764]uncertain significance11645191116451911Humanname
405807608CV3356507single nucleotide variantNM_018090.5(NECAP2):c.568C>T (p.Pro190Ser)not specified [RCV004480767]uncertain significance11645191616451916Humanname
405807614CV3356510single nucleotide variantNM_018090.5(NECAP2):c.575C>G (p.Pro192Arg)not specified [RCV004480770]uncertain significance11645192316451923Humanname
405807619CV3356513single nucleotide variantNM_018090.5(NECAP2):c.584A>C (p.Lys195Thr)not specified [RCV004480773]uncertain significance11645193216451932Humanname
405807623CV3356515single nucleotide variantNM_018090.5(NECAP2):c.749C>A (p.Thr250Asn)not specified [RCV004480775]uncertain significance11645884716458847Humanname
407489380CV3454781single nucleotide variantNM_018090.5(NECAP2):c.532C>T (p.Arg178Trp)not specified [RCV004641457]uncertain significance11645188016451880Humanname
407489387CV3454783single nucleotide variantNM_018090.5(NECAP2):c.491A>T (p.Asn164Ile)not specified [RCV004641458]uncertain significance11645183916451839Humanname
407489392CV3454784single nucleotide variantNM_018090.5(NECAP2):c.557G>C (p.Ser186Thr)not specified [RCV004641459]uncertain significance11645190516451905Humanname
597670130CV3555786single nucleotide variantNM_018090.5(NECAP2):c.362C>T (p.Ala121Val)not specified [RCV004829644]uncertain significance11644812316448123Humanname
597670138CV3555787single nucleotide variantNM_018090.5(NECAP2):c.527G>C (p.Arg176Pro)not specified [RCV004829645]uncertain significance11645187516451875Humanname
597670147CV3555788single nucleotide variantNM_018090.5(NECAP2):c.328G>A (p.Gly110Arg)not specified [RCV004829646]uncertain significance11644808916448089Humanname
598231419CV3990606single nucleotide variantNM_018090.5(NECAP2):c.548G>A (p.Gly183Glu)not specified [RCV005381355]uncertain significance11645189616451896Humanname