Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.26419708A>T | CA1160061489 | LIN28A | c.229-5595A>T (n.229-5595A>T) | dbSNP |
1 | g.26419708A>C | CA1160061488 | LIN28A | c.229-5595A>C (n.229-5595A>C) | dbSNP |
1 | g.26419708A>G | CA15078059 | LIN28A | c.229-5595A>G (n.229-5595A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |