Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.99153883T>G | CA10630737 | TGFBR1 | c.*4578T>G (n.*4578T>G) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.99153883T>C | CA869146553 | TGFBR1 | c.*4578T>C (n.*4578T>C) | dbSNP gnomAD v3 gnomAD v4 |
9 | g.99153883T= | CA1630847906 | TGFBR1 | c.*4578T= (n.*4578T=) | dbSNP |