Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.108591087C>ACA413932226COL4A5c.1195C>A (p.Pro399Thr)
n.651C>A
c.871C>A (p.Pro291Thr)
c.1210C>A (p.Pro404Thr)
c.-515C>A (n.-515C>A)
Xg.108591087C>GCA413932227COL4A5c.1195C>G (p.Pro399Ala)
n.651C>G
c.871C>G (p.Pro291Ala)
c.1210C>G (p.Pro404Ala)
c.-515C>G (n.-515C>G)
gnomAD v4
Xg.108591087C>TCA413932229COL4A5c.1195C>T (p.Pro399Ser)
n.651C>T
c.871C>T (p.Pro291Ser)
c.1210C>T (p.Pro404Ser)
c.-515C>T (n.-515C>T)
Xg.108591088C>ACA413932232COL4A5c.1196C>A (p.Pro399His)
n.652C>A
c.872C>A (p.Pro291His)
c.1211C>A (p.Pro404His)
c.-514C>A (n.-514C>A)
Xg.108591088C>GCA413932244COL4A5c.1196C>G (p.Pro399Arg)
n.652C>G
c.872C>G (p.Pro291Arg)
c.1211C>G (p.Pro404Arg)
c.-514C>G (n.-514C>G)
Xg.108591088C>TCA413932234COL4A5c.1196C>T (p.Pro399Leu)
n.652C>T
c.872C>T (p.Pro291Leu)
c.1211C>T (p.Pro404Leu)
c.-514C>T (n.-514C>T)
gnomAD v4
Xg.108591089T>ACA517992155COL4A5c.1197T>A (p.Pro399=)
n.653T>A
c.873T>A (p.Pro291=)
c.1212T>A (p.Pro404=)
c.-513T>A (n.-513T>A)
Xg.108591089T>CCA517992156COL4A5c.1197T>C (p.Pro399=)
n.653T>C
c.873T>C (p.Pro291=)
c.1212T>C (p.Pro404=)
c.-513T>C (n.-513T>C)
Xg.108591089T>GCA517992157COL4A5c.1197T>G (p.Pro399=)
n.653T>G
c.873T>G (p.Pro291=)
c.1212T>G (p.Pro404=)
c.-513T>G (n.-513T>G)
Xg.108591090G>ACA413932247COL4A5c.1198G>A (p.Gly400Arg)
n.654G>A
c.874G>A (p.Gly292Arg)
c.1213G>A (p.Gly405Arg)
c.-512G>A (n.-512G>A)
Xg.108591090G>CCA413932249COL4A5c.1198G>C (p.Gly400Arg)
n.654G>C
c.874G>C (p.Gly292Arg)
c.1213G>C (p.Gly405Arg)
c.-512G>C (n.-512G>C)
Xg.108591090G=CA2450686396COL4A5c.1198G= (p.Gly400=)
n.654G=
c.874G= (p.Gly292=)
c.1213G= (p.Gly405=)
c.-512G= (n.-512G=)
Xg.108591090G>TCA413932251COL4A5c.1198G>T (p.Gly400Ter)
n.654G>T
c.874G>T (p.Gly292Ter)
c.1213G>T (p.Gly405Ter)
c.-512G>T (n.-512G>T)
ClinVar dbSNP
Xg.108591091G>ACA258420COL4A5c.1199G>A (p.Gly400Glu)
n.655G>A
c.875G>A (p.Gly292Glu)
c.1214G>A (p.Gly405Glu)
c.-511G>A (n.-511G>A)
ClinVar dbSNP
Xg.108591091G>CCA413932253COL4A5c.1199G>C (p.Gly400Ala)
n.655G>C
c.875G>C (p.Gly292Ala)
c.1214G>C (p.Gly405Ala)
c.-511G>C (n.-511G>C)
Xg.108591091G=CA2450686397COL4A5c.1199G= (p.Gly400=)
n.655G=
c.875G= (p.Gly292=)
c.1214G= (p.Gly405=)
c.-511G= (n.-511G=)
Xg.108591091G>TCA413932254COL4A5c.1199G>T (p.Gly400Val)
n.655G>T
c.875G>T (p.Gly292Val)
c.1214G>T (p.Gly405Val)
c.-511G>T (n.-511G>T)
Xg.108591092A>CCA517992158COL4A5c.1200A>C (p.Gly400=)
n.656A>C
c.876A>C (p.Gly292=)
c.1215A>C (p.Gly405=)
c.-510A>C (n.-510A>C)
Xg.108591092A>GCA517992159COL4A5c.1200A>G (p.Gly400=)
n.656A>G
c.876A>G (p.Gly292=)
c.1215A>G (p.Gly405=)
c.-510A>G (n.-510A>G)
COSMIC COSMIC
Xg.108591092A>TCA517992160COL4A5c.1200A>T (p.Gly400=)
n.656A>T
c.876A>T (p.Gly292=)
c.1215A>T (p.Gly405=)
c.-510A>T (n.-510A>T)
Xg.108591093T>ACA413932257COL4A5c.1201T>A (p.Phe401Ile)
n.657T>A
c.877T>A (p.Phe293Ile)
c.1216T>A (p.Phe406Ile)
c.-509T>A (n.-509T>A)
Xg.108591093T>CCA413932260COL4A5c.1201T>C (p.Phe401Leu)
n.657T>C
c.877T>C (p.Phe293Leu)
c.1216T>C (p.Phe406Leu)
c.-509T>C (n.-509T>C)
Xg.108591093T>GCA413932263COL4A5c.1201T>G (p.Phe401Val)
n.657T>G
c.877T>G (p.Phe293Val)
c.1216T>G (p.Phe406Val)
c.-509T>G (n.-509T>G)
gnomAD v4
Xg.108591094T>ACA413932271COL4A5c.1202T>A (p.Phe401Tyr)
n.658T>A
c.878T>A (p.Phe293Tyr)
c.1217T>A (p.Phe406Tyr)
c.-508T>A (n.-508T>A)
Xg.108591094T>CCA413932269COL4A5c.1202T>C (p.Phe401Ser)
n.658T>C
c.878T>C (p.Phe293Ser)
c.1217T>C (p.Phe406Ser)
c.-508T>C (n.-508T>C)
Xg.108591094T>GCA413932266COL4A5c.1202T>G (p.Phe401Cys)
n.658T>G
c.878T>G (p.Phe293Cys)
c.1217T>G (p.Phe406Cys)
c.-508T>G (n.-508T>G)
Xg.108591095T>ACA413932275COL4A5c.1203T>A (p.Phe401Leu)
n.659T>A
c.879T>A (p.Phe293Leu)
c.1218T>A (p.Phe406Leu)
c.-507T>A (n.-507T>A)
Xg.108591095T>CCA517992161COL4A5c.1203T>C (p.Phe401=)
n.659T>C
c.879T>C (p.Phe293=)
c.1218T>C (p.Phe406=)
c.-507T>C (n.-507T>C)
Xg.108591095T>GCA413932276COL4A5c.1203T>G (p.Phe401Leu)
n.659T>G
c.879T>G (p.Phe293Leu)
c.1218T>G (p.Phe406Leu)
c.-507T>G (n.-507T>G)
Xg.108591096C>ACA413932279COL4A5c.1204C>A (p.Pro402Thr)
n.660C>A
c.880C>A (p.Pro294Thr)
c.1219C>A (p.Pro407Thr)
c.-506C>A (n.-506C>A)
Xg.108591096C>GCA413932281COL4A5c.1204C>G (p.Pro402Ala)
n.660C>G
c.880C>G (p.Pro294Ala)
c.1219C>G (p.Pro407Ala)
c.-506C>G (n.-506C>G)
Xg.108591096C>TCA413932285COL4A5c.1204C>T (p.Pro402Ser)
n.660C>T
c.880C>T (p.Pro294Ser)
c.1219C>T (p.Pro407Ser)
c.-506C>T (n.-506C>T)
Xg.108591097C>ACA413932290COL4A5c.1205C>A (p.Pro402His)
n.661C>A
c.881C>A (p.Pro294His)
c.1220C>A (p.Pro407His)
c.-505C>A (n.-505C>A)
Xg.108591097C>GCA413932288COL4A5c.1205C>G (p.Pro402Arg)
n.661C>G
c.881C>G (p.Pro294Arg)
c.1220C>G (p.Pro407Arg)
c.-505C>G (n.-505C>G)
Xg.108591097C>TCA413932287COL4A5c.1205C>T (p.Pro402Leu)
n.661C>T
c.881C>T (p.Pro294Leu)
c.1220C>T (p.Pro407Leu)
c.-505C>T (n.-505C>T)
Xg.108591098T>ACA517992164COL4A5c.1206T>A (p.Pro402=)
n.662T>A
c.882T>A (p.Pro294=)
c.1221T>A (p.Pro407=)
c.-504T>A (n.-504T>A)
Xg.108591098T>CCA517992162COL4A5c.1206T>C (p.Pro402=)
n.662T>C
c.882T>C (p.Pro294=)
c.1221T>C (p.Pro407=)
c.-504T>C (n.-504T>C)
Xg.108591098T>GCA517992163COL4A5c.1206T>G (p.Pro402=)
n.662T>G
c.882T>G (p.Pro294=)
c.1221T>G (p.Pro407=)
c.-504T>G (n.-504T>G)
gnomAD v4
Xg.108591099G>ACA413932293COL4A5c.1207G>A (p.Gly403Arg)
n.663G>A
c.883G>A (p.Gly295Arg)
c.1222G>A (p.Gly408Arg)
c.-503G>A (n.-503G>A)
Xg.108591099G>CCA413932295COL4A5c.1207G>C (p.Gly403Arg)
n.663G>C
c.883G>C (p.Gly295Arg)
c.1222G>C (p.Gly408Arg)
c.-503G>C (n.-503G>C)
Xg.108591099G>TCA413932299COL4A5c.1207G>T (p.Gly403Ter)
n.663G>T
c.883G>T (p.Gly295Ter)
c.1222G>T (p.Gly408Ter)
c.-503G>T (n.-503G>T)
Xg.108591100G>ACA413932302COL4A5c.1208G>A (p.Gly403Glu)
n.664G>A
c.884G>A (p.Gly295Glu)
c.1223G>A (p.Gly408Glu)
c.-502G>A (n.-502G>A)
ClinVar
Xg.108591100G>CCA413932305COL4A5c.1208G>C (p.Gly403Ala)
n.664G>C
c.884G>C (p.Gly295Ala)
c.1223G>C (p.Gly408Ala)
c.-502G>C (n.-502G>C)
Xg.108591100G=CA2450686398COL4A5c.1208G= (p.Gly403=)
n.664G=
c.884G= (p.Gly295=)
c.1223G= (p.Gly408=)
c.-502G= (n.-502G=)
Xg.108591100G>TCA258422COL4A5c.1208G>T (p.Gly403Val)
n.664G>T
c.884G>T (p.Gly295Val)
c.1223G>T (p.Gly408Val)
c.-502G>T (n.-502G>T)
dbSNP
Xg.108591101A>CCA517992165COL4A5c.1209A>C (p.Gly403=)
n.665A>C
c.885A>C (p.Gly295=)
c.1224A>C (p.Gly408=)
c.-501A>C (n.-501A>C)
Xg.108591101A>GCA517992166COL4A5c.1209A>G (p.Gly403=)
n.665A>G
c.885A>G (p.Gly295=)
c.1224A>G (p.Gly408=)
c.-501A>G (n.-501A>G)
Xg.108591101A>TCA517992167COL4A5c.1209A>T (p.Gly403=)
n.665A>T
c.885A>T (p.Gly295=)
c.1224A>T (p.Gly408=)
c.-501A>T (n.-501A>T)
Xg.108591102G>ACA413932310COL4A5c.1210G>A (p.Glu404Lys)
n.666G>A
c.886G>A (p.Glu296Lys)
c.1225G>A (p.Glu409Lys)
c.-500G>A (n.-500G>A)
Xg.108591102G>CCA413932312COL4A5c.1210G>C (p.Glu404Gln)
n.666G>C
c.886G>C (p.Glu296Gln)
c.1225G>C (p.Glu409Gln)
c.-500G>C (n.-500G>C)

Number of alleles fetched