Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.71166082G>C | CA13726158 | TSPAN8 | c.-109-8295C>G (n.-109-8295C>G) n.207-8295C>G | dbSNP dbSNP dbSNP dbSNP dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.71166082G>A | CA691537331 | TSPAN8 | c.-109-8295C>T (n.-109-8295C>T) n.207-8295C>T | dbSNP |
12 | g.71166082G= | CA2045169924 | TSPAN8 | c.-109-8295C= (n.-109-8295C=) n.207-8295C= | dbSNP |