Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.71777771T>A | CA798105213 | GC | c.58+6190A>T (n.58+6190A>T) c.115+6190A>T (n.115+6190A>T) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.71777771T>C | CA11907159 | GC | c.58+6190A>G (n.58+6190A>G) c.115+6190A>G (n.115+6190A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |