Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.186603866A>T | CA3165298 | FAT1 | c.10660T>A (p.Ser3554Thr) c.10666T>A (p.Ser3556Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.186603866A>C | CA3165297 | FAT1 | c.10660T>G (p.Ser3554Ala) c.10666T>G (p.Ser3556Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.186603866A>G | CA358976865 | FAT1 | c.10660T>C (p.Ser3554Pro) c.10666T>C (p.Ser3556Pro) | dbSNP |
4 | g.186603866A= | CA1520094250 | FAT1 | c.10660T= (p.Ser3554=) c.10666T= (p.Ser3556=) | dbSNP |