Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.76983340_76983345delinsCAAGTACA1795350826PEX2c.834_839delinsTACTTG (p.Phe278=)
8g.76983346_76983350delCA16041186PEX2c.834_838del (p.Phe278LeufsTer3)
ClinVar dbSNP
8g.76983345A=CA1795350835PEX2c.834T= (p.Phe278=)
8g.76983345A>CCA371556464PEX2c.834T>G (p.Phe278Leu)
8g.76983345A>GCA4788644PEX2c.834T>C (p.Phe278=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
8g.76983345A>TCA371556465PEX2c.834T>A (p.Phe278Leu)
8g.76983346A>CCA371556468PEX2c.833T>G (p.Phe278Cys)
8g.76983346A>GCA371556467PEX2c.833T>C (p.Phe278Ser)
8g.76983346A>TCA371556466PEX2c.833T>A (p.Phe278Tyr)
8g.76983347_76983350dupCA918294494PEX2c.830_833dup (p.Phe278LeufsTer6)
dbSNP
8g.76983347A>CCA371556469PEX2c.832T>G (p.Phe278Val)
8g.76983347A>GCA371556470PEX2c.832T>C (p.Phe278Leu)
8g.76983347A>TCA371556471PEX2c.832T>A (p.Phe278Ile)
8g.76983348G>ACA461773142PEX2c.831C>T (p.Tyr277=)
ClinVar dbSNP gnomAD v3 gnomAD v4
8g.76983348G>CCA371556472PEX2c.831C>G (p.Tyr277Ter)
8g.76983348G=CA1795350838PEX2c.831C= (p.Tyr277=)
8g.76983348G>TCA371556473PEX2c.831C>A (p.Tyr277Ter)
8g.76983348delinsTAAGAAACCA2695201487PEX2c.831delinsGTTTCTTA (p.Tyr277Ter)
ClinVar
8g.76983349T>ACA371556474PEX2c.830A>T (p.Tyr277Phe)
8g.76983349T>CCA371556475PEX2c.830A>G (p.Tyr277Cys)
ClinVar dbSNP gnomAD v2 gnomAD v4
8g.76983349T>GCA371556476PEX2c.830A>C (p.Tyr277Ser)
gnomAD v4
8g.76983349T=CA1795350840PEX2c.830A= (p.Tyr277=)
8g.76983350A>CCA371556477PEX2c.829T>G (p.Tyr277Asp)
gnomAD v4
8g.76983350A>GCA371556478PEX2c.829T>C (p.Tyr277His)
8g.76983350A>TCA371556479PEX2c.829T>A (p.Tyr277Asn)
8g.76983351C>ACA461773143PEX2c.828G>T (p.Val276=)
8g.76983351C>GCA461773144PEX2c.828G>C (p.Val276=)
8g.76983351C>TCA461773145PEX2c.828G>A (p.Val276=)
ClinVar
8g.76983352A=CA1795350842PEX2c.827T= (p.Val276=)
8g.76983352A>CCA371556482PEX2c.827T>G (p.Val276Gly)
8g.76983352A>GCA371556481PEX2c.827T>C (p.Val276Ala)
dbSNP gnomAD v3 gnomAD v4
8g.76983352A>TCA371556480PEX2c.827T>A (p.Val276Glu)
8g.76983353C>ACA371556483PEX2c.826G>T (p.Val276Leu)
8g.76983353C=CA1795350848PEX2c.826G= (p.Val276=)
8g.76983353C>GCA4788645PEX2c.826G>C (p.Val276Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.76983353C>TCA4788646PEX2c.826G>A (p.Val276Met)
dbSNP ExAC gnomAD v2 gnomAD v4
8g.76983354G>ACA4788647PEX2c.825C>T (p.Asp275=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
8g.76983354G>CCA371556484PEX2c.825C>G (p.Asp275Glu)
8g.76983354G=CA1795350850PEX2c.825C= (p.Asp275=)
8g.76983354G>TCA371556485PEX2c.825C>A (p.Asp275Glu)
8g.76983355T>ACA371556488PEX2c.824A>T (p.Asp275Val)
8g.76983355T>CCA371556486PEX2c.824A>G (p.Asp275Gly)
8g.76983355T>GCA371556487PEX2c.824A>C (p.Asp275Ala)
8g.76983356C>ACA371556489PEX2c.823G>T (p.Asp275Tyr)
8g.76983356C=CA1795350853PEX2c.823G= (p.Asp275=)
8g.76983356C>GCA371556490PEX2c.823G>C (p.Asp275His)
dbSNP gnomAD v4
8g.76983356C>TCA371556491PEX2c.823G>A (p.Asp275Asn)
gnomAD v4
8g.76983357A>CCA371556492PEX2c.822T>G (p.Phe274Leu)
8g.76983357A>GCA461773146PEX2c.822T>C (p.Phe274=)
8g.76983357A>TCA371556493PEX2c.822T>A (p.Phe274Leu)

Number of alleles fetched