Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.93156525G>T | CA13693087 | n.427+59057C>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 | |
12 | g.93156525G>C | CA2055226329 | n.427+59057C>G | dbSNP | |
12 | g.93156525G>A | CA2055226328 | n.427+59057C>T | dbSNP | |
12 | g.93156525G= | CA2055226327 | n.427+59057C= | dbSNP |