Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.70450307A>G | CA49795534 | TGFA | c.*552T>C (n.*552T>C) c.379-686T>C c.*19-686T>C (n.*19-686T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.70450307A>C | CA892591288 | TGFA | c.*552T>G (n.*552T>G) c.379-686T>G c.*19-686T>G (n.*19-686T>G) | dbSNP gnomAD v3 gnomAD v4 |