Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.38774374dupCA551139737TLR10c.1220dup (p.Asn407LysfsTer6)
c.1178dup (p.Asn393LysfsTer6)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.38774374T>ACA356604640TLR10c.1217A>T (p.Gln406Leu)
c.1175A>T (p.Gln392Leu)
4g.38774374T>CCA356604639TLR10c.1217A>G (p.Gln406Arg)
c.1175A>G (p.Gln392Arg)
4g.38774374T>GCA356604638TLR10c.1217A>C (p.Gln406Pro)
c.1175A>C (p.Gln392Pro)
4g.38774374_38774387delinsTGACTCAGATCCAACA1451835021TLR10c.1204_1217delinsTTGGATCTGAGTCA (p.Leu402=)
c.1162_1175delinsTTGGATCTGAGTCA (p.Leu388=)
4g.38774375G>ACA356604641TLR10c.1216C>T (p.Gln406Ter)
c.1174C>T (p.Gln392Ter)
dbSNP gnomAD v4
4g.38774375G>CCA356604642TLR10c.1216C>G (p.Gln406Glu)
c.1174C>G (p.Gln392Glu)
4g.38774375G=CA1451835054TLR10c.1216C= (p.Gln406=)
c.1174C= (p.Gln392=)
4g.38774375G>TCA356604643TLR10c.1216C>A (p.Gln406Lys)
c.1174C>A (p.Gln392Lys)
gnomAD v4
4g.38774376_38774388delCA2888959TLR10c.1204_1216del (p.Leu402LysfsTer21)
c.1162_1174del (p.Leu388LysfsTer21)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.38774376A>CCA356604644TLR10c.1215T>G (p.Ser405Arg)
c.1173T>G (p.Ser391Arg)
4g.38774376A>GCA439132290TLR10c.1215T>C (p.Ser405=)
c.1173T>C (p.Ser391=)
4g.38774376A>TCA356604645TLR10c.1215T>A (p.Ser405Arg)
c.1173T>A (p.Ser391Arg)
4g.38774377C>ACA356604646TLR10c.1214G>T (p.Ser405Ile)
c.1172G>T (p.Ser391Ile)
4g.38774377C>GCA356604648TLR10c.1214G>C (p.Ser405Thr)
c.1172G>C (p.Ser391Thr)
gnomAD v4
4g.38774377C>TCA356604647TLR10c.1214G>A (p.Ser405Asn)
c.1172G>A (p.Ser391Asn)
4g.38774378T>ACA356604649TLR10c.1213A>T (p.Ser405Cys)
c.1171A>T (p.Ser391Cys)
4g.38774378T>CCA356604650TLR10c.1213A>G (p.Ser405Gly)
c.1171A>G (p.Ser391Gly)
gnomAD v4
4g.38774378T>GCA356604651TLR10c.1213A>C (p.Ser405Arg)
c.1171A>C (p.Ser391Arg)
4g.38774379C>ACA439132300TLR10c.1212G>T (p.Leu404=)
c.1170G>T (p.Leu390=)
4g.38774379C=CA1451835059TLR10c.1212G= (p.Leu404=)
c.1170G= (p.Leu390=)
4g.38774379C>GCA439132301TLR10c.1212G>C (p.Leu404=)
c.1170G>C (p.Leu390=)
dbSNP gnomAD v2 gnomAD v4
4g.38774379C>TCA439132299TLR10c.1212G>A (p.Leu404=)
c.1170G>A (p.Leu390=)
dbSNP gnomAD v4
4g.38774380A=CA1451835068TLR10c.1211T= (p.Leu404=)
c.1169T= (p.Leu390=)
4g.38774380A>CCA356604652TLR10c.1211T>G (p.Leu404Arg)
c.1169T>G (p.Leu390Arg)
4g.38774380A>GCA2888960TLR10c.1211T>C (p.Leu404Pro)
c.1169T>C (p.Leu390Pro)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.38774380A>TCA356604653TLR10c.1211T>A (p.Leu404Gln)
c.1169T>A (p.Leu390Gln)
4g.38774381G>ACA439132305TLR10c.1210C>T (p.Leu404=)
c.1168C>T (p.Leu390=)
gnomAD v4
4g.38774381G>CCA356604654TLR10c.1210C>G (p.Leu404Val)
c.1168C>G (p.Leu390Val)
4g.38774381G>TCA356604655TLR10c.1210C>A (p.Leu404Met)
c.1168C>A (p.Leu390Met)
gnomAD v4
4g.38774382A>CCA356604656TLR10c.1209T>G (p.Asp403Glu)
c.1167T>G (p.Asp389Glu)
4g.38774382A>GCA439132308TLR10c.1209T>C (p.Asp403=)
c.1167T>C (p.Asp389=)
4g.38774382A>TCA356604657TLR10c.1209T>A (p.Asp403Glu)
c.1167T>A (p.Asp389Glu)
4g.38774383T>ACA356604660TLR10c.1208A>T (p.Asp403Val)
c.1166A>T (p.Asp389Val)
4g.38774383T>CCA356604659TLR10c.1208A>G (p.Asp403Gly)
c.1166A>G (p.Asp389Gly)
gnomAD v4
4g.38774383T>GCA356604658TLR10c.1208A>C (p.Asp403Ala)
c.1166A>C (p.Asp389Ala)
4g.38774389_38774397delCA2670339566TLR10c.1200_1208del (p.Glu400_Leu402del)
c.1158_1166del (p.Glu386_Leu388del)
gnomAD v4
4g.38774384C>ACA356604661TLR10c.1207G>T (p.Asp403Tyr)
c.1165G>T (p.Asp389Tyr)
4g.38774384C>GCA356604662TLR10c.1207G>C (p.Asp403His)
c.1165G>C (p.Asp389His)
4g.38774384C>TCA356604663TLR10c.1207G>A (p.Asp403Asn)
c.1165G>A (p.Asp389Asn)
4g.38774385C>ACA356604664TLR10c.1206G>T (p.Leu402Phe)
c.1164G>T (p.Leu388Phe)
4g.38774385C>GCA356604665TLR10c.1206G>C (p.Leu402Phe)
c.1164G>C (p.Leu388Phe)
gnomAD v4
4g.38774385C>TCA439132314TLR10c.1206G>A (p.Leu402=)
c.1164G>A (p.Leu388=)
4g.38774386A>CCA356604666TLR10c.1205T>G (p.Leu402Trp)
c.1163T>G (p.Leu388Trp)
4g.38774386A>GCA356604667TLR10c.1205T>C (p.Leu402Ser)
c.1163T>C (p.Leu388Ser)
4g.38774386A>TCA356604668TLR10c.1205T>A (p.Leu402Ter)
c.1163T>A (p.Leu388Ter)
4g.38774387A>CCA356604669TLR10c.1204T>G (p.Leu402Val)
c.1162T>G (p.Leu388Val)
4g.38774387A>GCA439132317TLR10c.1204T>C (p.Leu402=)
c.1162T>C (p.Leu388=)
4g.38774387A>TCA356604670TLR10c.1204T>A (p.Leu402Met)
c.1162T>A (p.Leu388Met)
gnomAD v4
4g.38774388G>ACA439132318TLR10c.1203C>T (p.His401=)
c.1161C>T (p.His387=)

Number of alleles fetched