Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.57098300G>A | CA143831 | IL17RD | c.1403C>T (p.Ser468Leu) c.971C>T (p.Ser324Leu) n.1340C>T c.1319C>T (p.Ser440Leu) c.1331C>T (p.Ser444Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.57098300G>C | CA74987423 | IL17RD | c.1403C>G (p.Ser468Trp) c.971C>G (p.Ser324Trp) n.1340C>G c.1319C>G (p.Ser440Trp) c.1331C>G (p.Ser444Trp) | dbSNP |
3 | g.57098300G= | CA1367040395 | IL17RD | c.1403C= (p.Ser468=) c.971C= (p.Ser324=) n.1340C= c.1319C= (p.Ser440=) c.1331C= (p.Ser444=) | dbSNP |