Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.196351556C>G | CA1431609538 | UBXN7 | c.*5129G>C (n.*5129G>C) | dbSNP |
3 | g.196351556C>A | CA90831447 | UBXN7 | c.*5129G>T (n.*5129G>T) | dbSNP |
3 | g.196351556C>T | CA90831451 | UBXN7 | c.*5129G>A (n.*5129G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |