Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.21077717G>T | CA373067719 | IFNB1 | c.153C>A (p.Tyr51Ter) | dbSNP |
9 | g.21077717G>A | CA5008644 | IFNB1 | c.153C>T (p.Tyr51=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
9 | g.21077717G>C | CA373067712 | IFNB1 | c.153C>G (p.Tyr51Ter) | dbSNP |
9 | g.21077717G= | CA1838675120 | IFNB1 | c.153C= (p.Tyr51=) | dbSNP |