Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.4608610G>A | CA10657194 | n.489+567G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 | |
1 | g.4608610G>C | CA1150659665 | n.489+567G>C | dbSNP | |
1 | g.4608610G= | CA1140002113 | n.489+567G= | dbSNP | |
1 | g.4608610G>T | CA3071610544 | n.489+567G>T | dbSNP |