Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
18 | g.51084461A>G | CA629582620 | SMAD4 | c.*5994A>G (n.*5994A>G) n.7761A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.51084461A>C | CA10651008 | SMAD4 | c.*5994A>C (n.*5994A>C) n.7761A>C | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.51084461A>T | CA780210820 | SMAD4 | c.*5994A>T (n.*5994A>T) n.7761A>T | dbSNP gnomAD v3 gnomAD v4 |