Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.67191781G>T | CA715090143 | SMAD3 | c.*1245G>T (n.*1245G>T) n.283-1092G>T | dbSNP |
15 | g.67191781G>A | CA10647311 | SMAD3 | c.*1245G>A (n.*1245G>A) n.283-1092G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |