Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.23419950G>T | CA038110 | MYH7 | c.3621C>A (p.Ile1207=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23419950G>A | CA013881 | MYH7 | c.3621C>T (p.Ile1207=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
14 | g.23419950G>C | CA038128 | MYH7 | c.3621C>G (p.Ile1207Met) | ClinVar dbSNP ExAC gnomAD v4 |