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Variants search result for Homo sapiens
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36 records found for search term Acap2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8578535CV112919single nucleotide variantNM_012287.5(ACAP2):c.344+786A>TLung cancer [RCV000093442]uncertain significance3195344473195344473Humanname
15144856CV708750single nucleotide variantNM_012287.6(ACAP2):c.81T>C (p.Asp27=)not provided [RCV000966899]likely benign3195392120195392120Humanname
156283704CV2317481single nucleotide variantNM_012287.6(ACAP2):c.13G>C (p.Val5Leu)not specified [RCV004172446]uncertain significance3195442835195442835Humanname
155924663CV2277161single nucleotide variantNM_012287.6(ACAP2):c.230A>T (p.Glu77Val)not specified [RCV004142804]uncertain significance3195381904195381904Humanname
407473653CV3427802single nucleotide variantNM_012287.6(ACAP2):c.226G>A (p.Val76Ile)not specified [RCV004600419]uncertain significance3195381908195381908Humanname
407473693CV3427812single nucleotide variantNM_012287.6(ACAP2):c.218A>G (p.Asp73Gly)not specified [RCV004600428]uncertain significance3195381916195381916Humanname
597804864CV3630593single nucleotide variantNM_012287.6(ACAP2):c.128T>C (p.Ile43Thr)not specified [RCV004882474]uncertain significance3195382006195382006Humanname
156183782CV2243367single nucleotide variantNM_012287.6(ACAP2):c.786T>G (p.Asp262Glu)not specified [RCV004112057]uncertain significance3195320772195320772Humanname
155938349CV2365013single nucleotide variantNM_012287.6(ACAP2):c.500G>A (p.Arg167Gln)not specified [RCV004224174]uncertain significance3195342499195342499Humanname
329374690CV2470669single nucleotide variantNM_012287.6(ACAP2):c.677G>A (p.Arg226Gln)not specified [RCV004273923]uncertain significance3195326952195326952Humanname
401759362CV2701514single nucleotide variantNM_012287.6(ACAP2):c.521T>G (p.Val174Gly)not specified [RCV004313965]uncertain significance3195342478195342478Humanname
405731599CV3294870single nucleotide variantNM_012287.6(ACAP2):c.802G>A (p.Val268Ile)not specified [RCV004429415]uncertain significance3195320756195320756Humanname
407473621CV3427792single nucleotide variantNM_012287.6(ACAP2):c.625C>A (p.Leu209Met)not specified [RCV004600411]uncertain significance3195333072195333072Humanname
597804880CV3630676single nucleotide variantNM_012287.6(ACAP2):c.755G>T (p.Ser252Ile)not specified [RCV004882506]uncertain significance3195320803195320803Humanname
598257600CV3933222single nucleotide variantNM_012287.6(ACAP2):c.794A>G (p.Asn265Ser)not specified [RCV005299858]uncertain significance3195320764195320764Humanname
598266958CV3933490single nucleotide variantNM_012287.6(ACAP2):c.797G>C (p.Gly266Ala)not specified [RCV005302066]uncertain significance3195320761195320761Humanname
598257200CV3936942single nucleotide variantNM_012287.6(ACAP2):c.596A>G (p.His199Arg)not specified [RCV005299770]uncertain significance3195333101195333101Humanname
156028143CV2238202single nucleotide variantNM_012287.6(ACAP2):c.1784C>T (p.Ser595Phe)not specified [RCV004113294]uncertain significance3195292434195292434Humanname
156034467CV2256699single nucleotide variantNM_012287.6(ACAP2):c.1787C>T (p.Ser596Phe)not specified [RCV004118873]uncertain significance3195292431195292431Humanname
156162830CV2323561single nucleotide variantNM_012287.6(ACAP2):c.1320T>G (p.Ile440Met)not specified [RCV004165757]uncertain significance3195301971195301971Humanname
156307168CV2335370single nucleotide variantNM_012287.6(ACAP2):c.2047G>A (p.Val683Ile)not specified [RCV004186926]uncertain significance3195291722195291722Humanname
155912721CV2341635single nucleotide variantNM_012287.6(ACAP2):c.2264G>A (p.Arg755His)not specified [RCV004182562]uncertain significance3195279401195279401Humanname
155928115CV2361863single nucleotide variantNM_012287.6(ACAP2):c.1784C>A (p.Ser595Tyr)not specified [RCV004207639]uncertain significance3195292434195292434Humanname
156175029CV2377212single nucleotide variantNM_012287.6(ACAP2):c.2288A>G (p.Asn763Ser)not specified [RCV004231881]uncertain significance3195279377195279377Humanname
329401706CV2461094single nucleotide variantNM_012287.6(ACAP2):c.1736C>T (p.Thr579Met)not specified [RCV004265237]uncertain significance3195294748195294748Humanname
329362713CV2467120single nucleotide variantNM_012287.6(ACAP2):c.1400T>C (p.Met467Thr)not specified [RCV004282850]uncertain significance3195297277195297277Humanname
401754927CV2682336single nucleotide variantNM_012287.6(ACAP2):c.1973A>G (p.Glu658Gly)not specified [RCV004290372]uncertain significance3195291796195291796Humanname
407473734CV3427823single nucleotide variantNM_012287.6(ACAP2):c.1025A>C (p.Gln342Pro)not specified [RCV004600438]uncertain significance3195306602195306602Humanname
407473773CV3427834single nucleotide variantNM_012287.6(ACAP2):c.1069C>G (p.Gln357Glu)not specified [RCV004600448]uncertain significance3195306558195306558Humanname
597751708CV3630428single nucleotide variantNM_012287.6(ACAP2):c.1118A>G (p.Lys373Arg)not specified [RCV004892806]uncertain significance3195302173195302173Humanname
597804763CV3630501single nucleotide variantNM_012287.6(ACAP2):c.2003A>G (p.Asn668Ser)not specified [RCV004882421]uncertain significance3195291766195291766Humanname
597804603CV3634217single nucleotide variantNM_012287.6(ACAP2):c.1211G>A (p.Arg404Gln)not specified [RCV004882337]uncertain significance3195302080195302080Humanname
598267376CV3929778single nucleotide variantNM_012287.6(ACAP2):c.1583A>C (p.Lys528Thr)not specified [RCV005302162]uncertain significance3195295797195295797Humanname
598257903CV3933319single nucleotide variantNM_012287.6(ACAP2):c.1894G>A (p.Val632Met)not specified [RCV005299916]uncertain significance3195292324195292324Humanname
598220237CV3933407single nucleotide variantNM_012287.6(ACAP2):c.1807C>T (p.His603Tyr)not specified [RCV005293453]uncertain significance3195292411195292411Humanname
598267170CV3933580single nucleotide variantNM_012287.6(ACAP2):c.1858C>T (p.Pro620Ser)not specified [RCV005302115]uncertain significance3195292360195292360Humanname