Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.186603866A>TCA3165298FAT1c.10660T>A (p.Ser3554Thr)
c.10666T>A (p.Ser3556Thr)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.186603866A>CCA3165297FAT1c.10660T>G (p.Ser3554Ala)
c.10666T>G (p.Ser3556Ala)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.186603866A>GCA358976865FAT1c.10660T>C (p.Ser3554Pro)
c.10666T>C (p.Ser3556Pro)
dbSNP
4g.186603866A=CA1520094250FAT1c.10660T= (p.Ser3554=)
c.10666T= (p.Ser3556=)
dbSNP

Number of alleles fetched