Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.211378697G>A | CA11344360 | ERBB4 | c.*4918C>T (n.*4918C>T) c.8719C>T (n.8719C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.211378697G= | CA1325460593 | ERBB4 | c.*4918C= (n.*4918C=) c.8719C= (n.8719C=) | dbSNP |