Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.61987926T>C | CA208309977 | ARID5B | c.503-12165T>C (n.503-12165T>C) c.502+47518T>C (n.502+47518T>C) c.-65-12165T>C (n.-65-12165T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.61987926T= | CA1914338183 | ARID5B | c.503-12165T= (n.503-12165T=) c.502+47518T= (n.502+47518T=) c.-65-12165T= (n.-65-12165T=) | dbSNP |