Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.169850328G>A | CA87600272 | LRRC31 | c.1159+1291C>T (n.1159+1291C>T) c.991+1291C>T (n.991+1291C>T) c.964+1291C>T (n.964+1291C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.169850328G>C | CA11427657 | LRRC31 | c.1159+1291C>G (n.1159+1291C>G) c.991+1291C>G (n.991+1291C>G) c.964+1291C>G (n.964+1291C>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |