Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.963799C>A | CA693826153 | RAD52 | c.-19+26010G>T (n.-19+26010G>T) | dbSNP |
12 | g.963799C>T | CA13771537 | RAD52 | c.-19+26010G>A (n.-19+26010G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.963799C= | CA2011758704 | RAD52 | c.-19+26010G= (n.-19+26010G=) | dbSNP |