Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.169765059C>G | CA343760 | TERC | n.2G>C | ClinVar dbSNP |
3 | g.169765059C>T | CA436716080 | TERC | n.2G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
3 | g.169765059C= | CA1419573696 | TERC | n.2G= | dbSNP |
3 | g.169765059C>A | CA436716079 | TERC | n.2G>T | dbSNP gnomAD v4 |