Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.92975544C>G | CA13467238 | MTNR1B | c.223+5596C>G (n.223+5596C>G) c.165+5596C>G c.354+2953C>G (n.354+2953C>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.92975544C>T | CA1991754954 | MTNR1B | c.223+5596C>T (n.223+5596C>T) c.165+5596C>T c.354+2953C>T (n.354+2953C>T) | dbSNP |