Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.115768384G>ACA1843119DPP10c.1201G>A (p.Val401Ile)
c.1180G>A (p.Val394Ile)
c.1213G>A (p.Val405Ile)
c.1051G>A (p.Val351Ile)
c.949G>A (p.Val317Ile)
c.1078G>A (p.Val360Ile)
c.1141G>A (p.Val381Ile)
c.1189G>A (p.Val397Ile)
c.1252G>A (p.Val418Ile)
c.1162G>A (p.Val388Ile)
c.1111G>A (p.Val371Ile)
c.1084G>A (p.Val362Ile)
c.439G>A (p.Val147Ile)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.115768384G=CA1281319721DPP10c.1201G= (p.Val401=)
c.1180G= (p.Val394=)
c.1213G= (p.Val405=)
c.1051G= (p.Val351=)
c.949G= (p.Val317=)
c.1078G= (p.Val360=)
c.1141G= (p.Val381=)
c.1189G= (p.Val397=)
c.1252G= (p.Val418=)
c.1162G= (p.Val388=)
c.1111G= (p.Val371=)
c.1084G= (p.Val362=)
c.439G= (p.Val147=)
dbSNP

Number of alleles fetched