Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.202667581A>T | CA1321609183 | FAM117B | c.602-28300A>T (n.602-28300A>T) n.301-28300A>T | dbSNP |
2 | g.202667581A>G | CA11206750 | FAM117B | c.602-28300A>G (n.602-28300A>G) n.301-28300A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |