Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.1105714C>ACA402937501GPX4c.492C>A (p.Phe164Leu)
c.300C>A (p.Phe100Leu)
c.375C>A (p.Phe125Leu)
c.-4C>A (n.-4C>A)
c.381C>A (p.Phe127Leu)
c.114C>A (p.Phe38Leu)
c.261C>A (p.Phe87Leu)
n.320C>A
c.378C>A (p.Phe126Leu)
c.489C>A (p.Phe163Leu)
19g.1105714C=CA2317520100GPX4c.492C= (p.Phe164=)
c.300C= (p.Phe100=)
c.375C= (p.Phe125=)
c.-4C= (n.-4C=)
c.381C= (p.Phe127=)
c.114C= (p.Phe38=)
c.261C= (p.Phe87=)
n.320C=
c.378C= (p.Phe126=)
c.489C= (p.Phe163=)
19g.1105714C>GCA402937502GPX4c.492C>G (p.Phe164Leu)
c.300C>G (p.Phe100Leu)
c.375C>G (p.Phe125Leu)
c.-4C>G (n.-4C>G)
c.381C>G (p.Phe127Leu)
c.114C>G (p.Phe38Leu)
c.261C>G (p.Phe87Leu)
n.320C>G
c.378C>G (p.Phe126Leu)
c.489C>G (p.Phe163Leu)
dbSNP
19g.1105714C>TCA504694593GPX4c.492C>T (p.Phe164=)
c.300C>T (p.Phe100=)
c.375C>T (p.Phe125=)
c.-4C>T (n.-4C>T)
c.381C>T (p.Phe127=)
c.114C>T (p.Phe38=)
c.261C>T (p.Phe87=)
n.320C>T
c.378C>T (p.Phe126=)
c.489C>T (p.Phe163=)
dbSNP gnomAD v2 gnomAD v4
19g.1105715G>ACA402937503GPX4c.493G>A (p.Asp165Asn)
c.301G>A (p.Asp101Asn)
c.376G>A (p.Asp126Asn)
c.-3G>A (n.-3G>A)
c.382G>A (p.Asp128Asn)
c.115G>A (p.Asp39Asn)
c.262G>A (p.Asp88Asn)
n.321G>A
c.379G>A (p.Asp127Asn)
c.490G>A (p.Asp164Asn)
dbSNP gnomAD v2 gnomAD v4
19g.1105715G>CCA402937504GPX4c.493G>C (p.Asp165His)
c.301G>C (p.Asp101His)
c.376G>C (p.Asp126His)
c.-3G>C (n.-3G>C)
c.382G>C (p.Asp128His)
c.115G>C (p.Asp39His)
c.262G>C (p.Asp88His)
n.321G>C
c.379G>C (p.Asp127His)
c.490G>C (p.Asp164His)
gnomAD v4
19g.1105715G=CA2317520101GPX4c.493G= (p.Asp165=)
c.301G= (p.Asp101=)
c.376G= (p.Asp126=)
c.-3G= (n.-3G=)
c.382G= (p.Asp128=)
c.115G= (p.Asp39=)
c.262G= (p.Asp88=)
n.321G=
c.379G= (p.Asp127=)
c.490G= (p.Asp164=)
19g.1105715G>TCA402937505GPX4c.493G>T (p.Asp165Tyr)
c.301G>T (p.Asp101Tyr)
c.376G>T (p.Asp126Tyr)
c.-3G>T (n.-3G>T)
c.382G>T (p.Asp128Tyr)
c.115G>T (p.Asp39Tyr)
c.262G>T (p.Asp88Tyr)
n.321G>T
c.379G>T (p.Asp127Tyr)
c.490G>T (p.Asp164Tyr)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1105716A=CA2317520102GPX4c.494A= (p.Asp165=)
c.302A= (p.Asp101=)
c.377A= (p.Asp126=)
c.-2A= (n.-2A=)
c.383A= (p.Asp128=)
c.116A= (p.Asp39=)
c.263A= (p.Asp88=)
n.322A=
c.380A= (p.Asp127=)
c.491A= (p.Asp164=)
19g.1105716A>CCA402937506GPX4c.494A>C (p.Asp165Ala)
c.302A>C (p.Asp101Ala)
c.377A>C (p.Asp126Ala)
c.-2A>C (n.-2A>C)
c.383A>C (p.Asp128Ala)
c.116A>C (p.Asp39Ala)
c.263A>C (p.Asp88Ala)
n.322A>C
c.380A>C (p.Asp127Ala)
c.491A>C (p.Asp164Ala)
19g.1105716A>GCA9037339GPX4c.494A>G (p.Asp165Gly)
c.302A>G (p.Asp101Gly)
c.377A>G (p.Asp126Gly)
c.-2A>G (n.-2A>G)
c.383A>G (p.Asp128Gly)
c.116A>G (p.Asp39Gly)
c.263A>G (p.Asp88Gly)
n.322A>G
c.380A>G (p.Asp127Gly)
c.491A>G (p.Asp164Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.1105716A>TCA9037338GPX4c.494A>T (p.Asp165Val)
c.302A>T (p.Asp101Val)
c.377A>T (p.Asp126Val)
c.-2A>T (n.-2A>T)
c.383A>T (p.Asp128Val)
c.116A>T (p.Asp39Val)
c.263A>T (p.Asp88Val)
n.322A>T
c.380A>T (p.Asp127Val)
c.491A>T (p.Asp164Val)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.1105717T>ACA402937508GPX4c.495T>A (p.Asp165Glu)
c.303T>A (p.Asp101Glu)
c.378T>A (p.Asp126Glu)
c.-1T>A (n.-1T>A)
c.384T>A (p.Asp128Glu)
c.117T>A (p.Asp39Glu)
c.264T>A (p.Asp88Glu)
n.323T>A
c.381T>A (p.Asp127Glu)
c.492T>A (p.Asp164Glu)
19g.1105717T>CCA9037340GPX4c.495T>C (p.Asp165=)
c.303T>C (p.Asp101=)
c.378T>C (p.Asp126=)
c.-1T>C (n.-1T>C)
c.384T>C (p.Asp128=)
c.117T>C (p.Asp39=)
c.264T>C (p.Asp88=)
n.323T>C
c.381T>C (p.Asp127=)
c.492T>C (p.Asp164=)
dbSNP ExAC gnomAD v2
19g.1105717T>GCA402937507GPX4c.495T>G (p.Asp165Glu)
c.303T>G (p.Asp101Glu)
c.378T>G (p.Asp126Glu)
c.-1T>G (n.-1T>G)
c.384T>G (p.Asp128Glu)
c.117T>G (p.Asp39Glu)
c.264T>G (p.Asp88Glu)
n.323T>G
c.381T>G (p.Asp127Glu)
c.492T>G (p.Asp164Glu)
19g.1105717T=CA2317520103GPX4c.495T= (p.Asp165=)
c.303T= (p.Asp101=)
c.378T= (p.Asp126=)
c.-1T= (n.-1T=)
c.384T= (p.Asp128=)
c.117T= (p.Asp39=)
c.264T= (p.Asp88=)
n.323T=
c.381T= (p.Asp127=)
c.492T= (p.Asp164=)
19g.1105718A=CA2317520104GPX4c.496A= (p.Met166=)
c.304A= (p.Met102=)
c.379A= (p.Met127=)
c.1A= (p.Met1=)
c.385A= (p.Met129=)
c.118A= (p.Met40=)
c.265A= (p.Met89=)
n.324A=
c.382A= (p.Met128=)
c.493A= (p.Met165=)
19g.1105718A>CCA402937509GPX4c.496A>C (p.Met166Leu)
c.304A>C (p.Met102Leu)
c.379A>C (p.Met127Leu)
c.1A>C (p.Met1Leu)
c.385A>C (p.Met129Leu)
c.118A>C (p.Met40Leu)
c.265A>C (p.Met89Leu)
n.324A>C
c.382A>C (p.Met128Leu)
c.493A>C (p.Met165Leu)
19g.1105718A>GCA9037341GPX4c.496A>G (p.Met166Val)
c.304A>G (p.Met102Val)
c.379A>G (p.Met127Val)
c.1A>G (p.Met1Val)
c.385A>G (p.Met129Val)
c.118A>G (p.Met40Val)
c.265A>G (p.Met89Val)
n.324A>G
c.382A>G (p.Met128Val)
c.493A>G (p.Met165Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.1105718A>TCA9037342GPX4c.496A>T (p.Met166Leu)
c.304A>T (p.Met102Leu)
c.379A>T (p.Met127Leu)
c.1A>T (p.Met1Leu)
c.385A>T (p.Met129Leu)
c.118A>T (p.Met40Leu)
c.265A>T (p.Met89Leu)
n.324A>T
c.382A>T (p.Met128Leu)
c.493A>T (p.Met165Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.1105719T>ACA402937510GPX4c.497T>A (p.Met166Lys)
c.305T>A (p.Met102Lys)
c.380T>A (p.Met127Lys)
c.2T>A (p.Met1Lys)
c.386T>A (p.Met129Lys)
c.119T>A (p.Met40Lys)
c.266T>A (p.Met89Lys)
n.325T>A
c.383T>A (p.Met128Lys)
c.494T>A (p.Met165Lys)
gnomAD v4
19g.1105719T>CCA402937511GPX4c.497T>C (p.Met166Thr)
c.305T>C (p.Met102Thr)
c.380T>C (p.Met127Thr)
c.2T>C (p.Met1Thr)
c.386T>C (p.Met129Thr)
c.119T>C (p.Met40Thr)
c.266T>C (p.Met89Thr)
n.325T>C
c.383T>C (p.Met128Thr)
c.494T>C (p.Met165Thr)
dbSNP
19g.1105719T>GCA402937512GPX4c.497T>G (p.Met166Arg)
c.305T>G (p.Met102Arg)
c.380T>G (p.Met127Arg)
c.2T>G (p.Met1Arg)
c.386T>G (p.Met129Arg)
c.119T>G (p.Met40Arg)
c.266T>G (p.Met89Arg)
n.325T>G
c.383T>G (p.Met128Arg)
c.494T>G (p.Met165Arg)
19g.1105719T=CA2317520105GPX4c.497T= (p.Met166=)
c.305T= (p.Met102=)
c.380T= (p.Met127=)
c.2T= (p.Met1=)
c.386T= (p.Met129=)
c.119T= (p.Met40=)
c.266T= (p.Met89=)
n.325T=
c.383T= (p.Met128=)
c.494T= (p.Met165=)
19g.1105720G>ACA402937513GPX4c.498G>A (p.Met166Ile)
c.306G>A (p.Met102Ile)
c.381G>A (p.Met127Ile)
c.3G>A (p.Met1Ile)
c.387G>A (p.Met129Ile)
c.120G>A (p.Met40Ile)
c.267G>A (p.Met89Ile)
n.326G>A
c.384G>A (p.Met128Ile)
c.495G>A (p.Met165Ile)
19g.1105720G>CCA402937514GPX4c.498G>C (p.Met166Ile)
c.306G>C (p.Met102Ile)
c.381G>C (p.Met127Ile)
c.3G>C (p.Met1Ile)
c.387G>C (p.Met129Ile)
c.120G>C (p.Met40Ile)
c.267G>C (p.Met89Ile)
n.326G>C
c.384G>C (p.Met128Ile)
c.495G>C (p.Met165Ile)
19g.1105720G>TCA402937515GPX4c.498G>T (p.Met166Ile)
c.306G>T (p.Met102Ile)
c.381G>T (p.Met127Ile)
c.3G>T (p.Met1Ile)
c.387G>T (p.Met129Ile)
c.120G>T (p.Met40Ile)
c.267G>T (p.Met89Ile)
n.326G>T
c.384G>T (p.Met128Ile)
c.495G>T (p.Met165Ile)
gnomAD v4
19g.1105721T>ACA402937516GPX4c.499T>A (p.Phe167Ile)
c.307T>A (p.Phe103Ile)
c.382T>A (p.Phe128Ile)
c.4T>A (p.Phe2Ile)
c.388T>A (p.Phe130Ile)
c.121T>A (p.Phe41Ile)
c.268T>A (p.Phe90Ile)
n.327T>A
c.385T>A (p.Phe129Ile)
c.496T>A (p.Phe166Ile)
19g.1105721T>CCA402937517GPX4c.499T>C (p.Phe167Leu)
c.307T>C (p.Phe103Leu)
c.382T>C (p.Phe128Leu)
c.4T>C (p.Phe2Leu)
c.388T>C (p.Phe130Leu)
c.121T>C (p.Phe41Leu)
c.268T>C (p.Phe90Leu)
n.327T>C
c.385T>C (p.Phe129Leu)
c.496T>C (p.Phe166Leu)
19g.1105721T>GCA402937518GPX4c.499T>G (p.Phe167Val)
c.307T>G (p.Phe103Val)
c.382T>G (p.Phe128Val)
c.4T>G (p.Phe2Val)
c.388T>G (p.Phe130Val)
c.121T>G (p.Phe41Val)
c.268T>G (p.Phe90Val)
n.327T>G
c.385T>G (p.Phe129Val)
c.496T>G (p.Phe166Val)
19g.1105722T>ACA402937521GPX4c.500T>A (p.Phe167Tyr)
c.308T>A (p.Phe103Tyr)
c.383T>A (p.Phe128Tyr)
c.5T>A (p.Phe2Tyr)
c.389T>A (p.Phe130Tyr)
c.122T>A (p.Phe41Tyr)
c.269T>A (p.Phe90Tyr)
n.328T>A
c.386T>A (p.Phe129Tyr)
c.497T>A (p.Phe166Tyr)
19g.1105722T>CCA402937520GPX4c.500T>C (p.Phe167Ser)
c.308T>C (p.Phe103Ser)
c.383T>C (p.Phe128Ser)
c.5T>C (p.Phe2Ser)
c.389T>C (p.Phe130Ser)
c.122T>C (p.Phe41Ser)
c.269T>C (p.Phe90Ser)
n.328T>C
c.386T>C (p.Phe129Ser)
c.497T>C (p.Phe166Ser)
19g.1105722T>GCA402937519GPX4c.500T>G (p.Phe167Cys)
c.308T>G (p.Phe103Cys)
c.383T>G (p.Phe128Cys)
c.5T>G (p.Phe2Cys)
c.389T>G (p.Phe130Cys)
c.122T>G (p.Phe41Cys)
c.269T>G (p.Phe90Cys)
n.328T>G
c.386T>G (p.Phe129Cys)
c.497T>G (p.Phe166Cys)
19g.1105723C>ACA402937522GPX4c.501C>A (p.Phe167Leu)
c.309C>A (p.Phe103Leu)
c.384C>A (p.Phe128Leu)
c.6C>A (p.Phe2Leu)
c.390C>A (p.Phe130Leu)
c.123C>A (p.Phe41Leu)
c.270C>A (p.Phe90Leu)
n.329C>A
c.387C>A (p.Phe129Leu)
c.498C>A (p.Phe166Leu)
gnomAD v4
19g.1105723C=CA2317520106GPX4c.501C= (p.Phe167=)
c.309C= (p.Phe103=)
c.384C= (p.Phe128=)
c.6C= (p.Phe2=)
c.390C= (p.Phe130=)
c.123C= (p.Phe41=)
c.270C= (p.Phe90=)
n.329C=
c.387C= (p.Phe129=)
c.498C= (p.Phe166=)
19g.1105723C>GCA402937523GPX4c.501C>G (p.Phe167Leu)
c.309C>G (p.Phe103Leu)
c.384C>G (p.Phe128Leu)
c.6C>G (p.Phe2Leu)
c.390C>G (p.Phe130Leu)
c.123C>G (p.Phe41Leu)
c.270C>G (p.Phe90Leu)
n.329C>G
c.387C>G (p.Phe129Leu)
c.498C>G (p.Phe166Leu)
19g.1105723C>TCA504694595GPX4c.501C>T (p.Phe167=)
c.309C>T (p.Phe103=)
c.384C>T (p.Phe128=)
c.6C>T (p.Phe2=)
c.390C>T (p.Phe130=)
c.123C>T (p.Phe41=)
c.270C>T (p.Phe90=)
n.329C>T
c.387C>T (p.Phe129=)
c.498C>T (p.Phe166=)
dbSNP gnomAD v2 gnomAD v4
19g.1105725_1105727delCA2576545100GPX4c.503_505del (p.Ser168del)
c.311_313del (p.Ser104del)
c.386_388del (p.Ser129del)
c.8_10del (p.Ser3del)
c.392_394del (p.Ser131del)
c.125_127del (p.Ser42del)
c.272_274del (p.Ser91del)
n.331_333del
c.389_391del (p.Ser130del)
c.500_502del (p.Ser167del)
19g.1105724A=CA2317520107GPX4c.502A= (p.Ser168=)
c.310A= (p.Ser104=)
c.385A= (p.Ser129=)
c.7A= (p.Ser3=)
c.391A= (p.Ser131=)
c.124A= (p.Ser42=)
c.271A= (p.Ser91=)
n.330A=
c.388A= (p.Ser130=)
c.499A= (p.Ser167=)
19g.1105724A>CCA402937524GPX4c.502A>C (p.Ser168Arg)
c.310A>C (p.Ser104Arg)
c.385A>C (p.Ser129Arg)
c.7A>C (p.Ser3Arg)
c.391A>C (p.Ser131Arg)
c.124A>C (p.Ser42Arg)
c.271A>C (p.Ser91Arg)
n.330A>C
c.388A>C (p.Ser130Arg)
c.499A>C (p.Ser167Arg)
19g.1105724A>GCA9037343GPX4c.502A>G (p.Ser168Gly)
c.310A>G (p.Ser104Gly)
c.385A>G (p.Ser129Gly)
c.7A>G (p.Ser3Gly)
c.391A>G (p.Ser131Gly)
c.124A>G (p.Ser42Gly)
c.271A>G (p.Ser91Gly)
n.330A>G
c.388A>G (p.Ser130Gly)
c.499A>G (p.Ser167Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.1105724A>TCA402937525GPX4c.502A>T (p.Ser168Cys)
c.310A>T (p.Ser104Cys)
c.385A>T (p.Ser129Cys)
c.7A>T (p.Ser3Cys)
c.391A>T (p.Ser131Cys)
c.124A>T (p.Ser42Cys)
c.271A>T (p.Ser91Cys)
n.330A>T
c.388A>T (p.Ser130Cys)
c.499A>T (p.Ser167Cys)
19g.1105725G>ACA402937526GPX4c.503G>A (p.Ser168Asn)
c.311G>A (p.Ser104Asn)
c.386G>A (p.Ser129Asn)
c.8G>A (p.Ser3Asn)
c.392G>A (p.Ser131Asn)
c.125G>A (p.Ser42Asn)
c.272G>A (p.Ser91Asn)
n.331G>A
c.389G>A (p.Ser130Asn)
c.500G>A (p.Ser167Asn)
19g.1105725G>CCA402937527GPX4c.503G>C (p.Ser168Thr)
c.311G>C (p.Ser104Thr)
c.386G>C (p.Ser129Thr)
c.8G>C (p.Ser3Thr)
c.392G>C (p.Ser131Thr)
c.125G>C (p.Ser42Thr)
c.272G>C (p.Ser91Thr)
n.331G>C
c.389G>C (p.Ser130Thr)
c.500G>C (p.Ser167Thr)
19g.1105725G>TCA402937528GPX4c.503G>T (p.Ser168Ile)
c.311G>T (p.Ser104Ile)
c.386G>T (p.Ser129Ile)
c.8G>T (p.Ser3Ile)
c.392G>T (p.Ser131Ile)
c.125G>T (p.Ser42Ile)
c.272G>T (p.Ser91Ile)
n.331G>T
c.389G>T (p.Ser130Ile)
c.500G>T (p.Ser167Ile)
19g.1105726C>ACA402937529GPX4c.504C>A (p.Ser168Arg)
c.312C>A (p.Ser104Arg)
c.387C>A (p.Ser129Arg)
c.9C>A (p.Ser3Arg)
c.393C>A (p.Ser131Arg)
c.126C>A (p.Ser42Arg)
c.273C>A (p.Ser91Arg)
n.332C>A
c.390C>A (p.Ser130Arg)
c.501C>A (p.Ser167Arg)
19g.1105726C>GCA402937530GPX4c.504C>G (p.Ser168Arg)
c.312C>G (p.Ser104Arg)
c.387C>G (p.Ser129Arg)
c.9C>G (p.Ser3Arg)
c.393C>G (p.Ser131Arg)
c.126C>G (p.Ser42Arg)
c.273C>G (p.Ser91Arg)
n.332C>G
c.390C>G (p.Ser130Arg)
c.501C>G (p.Ser167Arg)
gnomAD v4
19g.1105726C>TCA504694598GPX4c.504C>T (p.Ser168=)
c.312C>T (p.Ser104=)
c.387C>T (p.Ser129=)
c.9C>T (p.Ser3=)
c.393C>T (p.Ser131=)
c.126C>T (p.Ser42=)
c.273C>T (p.Ser91=)
n.332C>T
c.390C>T (p.Ser130=)
c.501C>T (p.Ser167=)
gnomAD v4
19g.1105727A>CCA402937531GPX4c.505A>C (p.Lys169Gln)
c.313A>C (p.Lys105Gln)
c.388A>C (p.Lys130Gln)
c.10A>C (p.Lys4Gln)
c.394A>C (p.Lys132Gln)
c.127A>C (p.Lys43Gln)
c.274A>C (p.Lys92Gln)
n.333A>C
c.391A>C (p.Lys131Gln)
c.502A>C (p.Lys168Gln)
19g.1105727A>GCA402937532GPX4c.505A>G (p.Lys169Glu)
c.313A>G (p.Lys105Glu)
c.388A>G (p.Lys130Glu)
c.10A>G (p.Lys4Glu)
c.394A>G (p.Lys132Glu)
c.127A>G (p.Lys43Glu)
c.274A>G (p.Lys92Glu)
n.333A>G
c.391A>G (p.Lys131Glu)
c.502A>G (p.Lys168Glu)

Number of alleles fetched