Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.76983337_76983344delCA2687718855PEX2c.835_842del (p.Thr279Ter)
gnomAD v4
8g.76983339A>CCA371556451PEX2c.840T>G (p.Cys280Trp)
8g.76983339A>GCA461773138PEX2c.840T>C (p.Cys280=)
8g.76983339A>TCA371556452PEX2c.840T>A (p.Cys280Ter)
8g.76983340C>ACA4788643PEX2c.839G>T (p.Cys280Phe)
dbSNP ExAC gnomAD v2 gnomAD v4
8g.76983340C=CA1795350827PEX2c.839G= (p.Cys280=)
8g.76983340C>GCA371556454PEX2c.839G>C (p.Cys280Ser)
8g.76983340C>TCA371556453PEX2c.839G>A (p.Cys280Tyr)
8g.76983340_76983345delinsCAAGTACA1795350826PEX2c.834_839delinsTACTTG (p.Phe278=)
8g.76983341A>CCA371556455PEX2c.838T>G (p.Cys280Gly)
8g.76983341A>GCA371556456PEX2c.838T>C (p.Cys280Arg)
8g.76983341A>TCA371556457PEX2c.838T>A (p.Cys280Ser)
8g.76983346_76983350delCA16041186PEX2c.834_838del (p.Phe278LeufsTer3)
ClinVar dbSNP
8g.76983342A>CCA461773139PEX2c.837T>G (p.Thr279=)
8g.76983342A>GCA461773141PEX2c.837T>C (p.Thr279=)
8g.76983342A>TCA461773140PEX2c.837T>A (p.Thr279=)
8g.76983343G>ACA371556458PEX2c.836C>T (p.Thr279Ile)
dbSNP gnomAD v3 gnomAD v4
8g.76983343G>CCA371556459PEX2c.836C>G (p.Thr279Ser)
8g.76983343G=CA1795350832PEX2c.836C= (p.Thr279=)
8g.76983343G>TCA371556460PEX2c.836C>A (p.Thr279Asn)
8g.76983344T>ACA371556461PEX2c.835A>T (p.Thr279Ser)
8g.76983344T>CCA371556462PEX2c.835A>G (p.Thr279Ala)
8g.76983344T>GCA371556463PEX2c.835A>C (p.Thr279Pro)
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=)

Number of alleles fetched