Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.102876898G>T | CA212281170 | AS3MT,BORCS7-ASMT | c.529-56G>T (n.529-56G>T) c.*536-56G>T (n.*536-56G>T) n.934-56G>T | dbSNP gnomAD v4 |
10 | g.102876898G>C | CA13334213 | AS3MT,BORCS7-ASMT | c.529-56G>C (n.529-56G>C) c.*536-56G>C (n.*536-56G>C) n.934-56G>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |