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Variants search result for Homo sapiens
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24 records found for search term Npvf
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156383761CV2220188single nucleotide variantNM_022150.3(NPVF):c.47C>T (p.Thr16Ile)not specified [RCV004095655]uncertain significance72522839325228393Humanname
597685814CV3566590single nucleotide variantNM_022150.3(NPVF):c.98C>T (p.Ser33Phe)not specified [RCV004838137]uncertain significance72522834225228342Humanname
401871208CV2783447single nucleotide variantNM_022150.3(NPVF):c.122A>G (p.Tyr41Cys)not specified [RCV004365791]uncertain significance72522831825228318Humanname
405693443CV3362420single nucleotide variantNM_022150.3(NPVF):c.168C>G (p.Ser56Arg)not specified [RCV004491168]uncertain significance72522699725226997Humanname
598219434CV3997890single nucleotide variantNM_022150.3(NPVF):c.190G>A (p.Asp64Asn)not specified [RCV005379339]uncertain significance72522697525226975Humanname
598264379CV3997892single nucleotide variantNM_022150.3(NPVF):c.142A>G (p.Arg48Gly)not specified [RCV005387743]uncertain significance72522702325227023Humanname
156066235CV2197161single nucleotide variantNM_022150.3(NPVF):c.466T>C (p.Cys156Arg)not specified [RCV004071582]uncertain significance72522669925226699Humanname
156300967CV2245012single nucleotide variantNM_022150.3(NPVF):c.520C>T (p.Pro174Ser)not specified [RCV004104742]uncertain significance72522664525226645Humanname
156183517CV2255344single nucleotide variantNM_022150.3(NPVF):c.434G>A (p.Ser145Asn)not specified [RCV004117714]uncertain significance72522673125226731Humanname
156210994CV2259848single nucleotide variantNM_022150.3(NPVF):c.321C>A (p.Asn107Lys)not specified [RCV004117105]uncertain significance72522684425226844Humanname
156272319CV2297148single nucleotide variantNM_022150.3(NPVF):c.493A>T (p.Thr165Ser)not specified [RCV004151044]uncertain significance72522667225226672Humanname
156345825CV2308893single nucleotide variantNM_022150.3(NPVF):c.568G>A (p.Ala190Thr)not specified [RCV004169185]uncertain significance72522514525225145Humanname
156083444CV2343015single nucleotide variantNM_022150.3(NPVF):c.367C>T (p.Arg123Cys)not specified [RCV004192617]uncertain significance72522679825226798Humanname
156339352CV2351570single nucleotide variantNM_022150.3(NPVF):c.403A>G (p.Thr135Ala)not specified [RCV004195291]uncertain significance72522676225226762Humanname
405693451CV3362421single nucleotide variantNM_022150.3(NPVF):c.435T>A (p.Ser145Arg)not specified [RCV004491169]uncertain significance72522673025226730Humanname
405693454CV3362422single nucleotide variantNM_022150.3(NPVF):c.488C>T (p.Ser163Phe)not specified [RCV004491170]uncertain significance72522667725226677Humanname
407516612CV3465720single nucleotide variantNM_022150.3(NPVF):c.377A>G (p.Asn126Ser)not specified [RCV004650338]uncertain significance72522678825226788Humanname
407476656CV3465721single nucleotide variantNM_022150.3(NPVF):c.368G>A (p.Arg123His)not specified [RCV004638637]likely benign72522679725226797Humanname
407516614CV3465722single nucleotide variantNM_022150.3(NPVF):c.463C>T (p.Pro155Ser)not specified [RCV004650339]uncertain significance72522670225226702Humanname
597642723CV3566588single nucleotide variantNM_022150.3(NPVF):c.523G>T (p.Asp175Tyr)not specified [RCV004832491]uncertain significance72522664225226642Humanname
597685825CV3566591single nucleotide variantNM_022150.3(NPVF):c.484T>C (p.Tyr162His)not specified [RCV004838138]uncertain significance72522668125226681Humanname
598219442CV3997891single nucleotide variantNM_022150.3(NPVF):c.322C>A (p.Leu108Met)not specified [RCV005379340]uncertain significance72522684325226843Humanname
598264384CV3997893single nucleotide variantNM_022150.3(NPVF):c.398G>A (p.Arg133Lys)not specified [RCV005387744]uncertain significance72522676725226767Humanname
598264390CV3997894single nucleotide variantNM_022150.3(NPVF):c.523G>A (p.Asp175Asn)not specified [RCV005387745]uncertain significance72522664225226642Humanname