Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.65371166T>A | CA11070488 | SPRED2 | c.27-26270A>T (n.27-26270A>T) c.71+6447A>T (n.71+6447A>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.65371166T>C | CA1257210622 | SPRED2 | c.27-26270A>G (n.27-26270A>G) c.71+6447A>G (n.71+6447A>G) | dbSNP |