Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.186603866A= | CA1520094250 | FAT1 | c.10660T= (p.Ser3554=) c.10666T= (p.Ser3556=) | |
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) | |
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.186603866_186603867delinsCA | CA2580071728 | FAT1 | c.10659_10660delinsTG (p.Ser3554Ala) c.10665_10666delinsTG (p.Ser3556Ala) | ClinVar |
4 | g.186603867G>A | CA3165299 | FAT1 | c.10659C>T (p.Thr3553=) c.10665C>T (p.Thr3555=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.186603867G>C | CA442889162 | FAT1 | c.10659C>G (p.Thr3553=) c.10665C>G (p.Thr3555=) | |
4 | g.186603867G= | CA1520094251 | FAT1 | c.10659C= (p.Thr3553=) c.10665C= (p.Thr3555=) | |
4 | g.186603867G>T | CA442889160 | FAT1 | c.10659C>A (p.Thr3553=) c.10665C>A (p.Thr3555=) | |
4 | g.186603868G>A | CA358976866 | FAT1 | c.10658C>T (p.Thr3553Ile) c.10664C>T (p.Thr3555Ile) | |
4 | g.186603868G>C | CA358976867 | FAT1 | c.10658C>G (p.Thr3553Ser) c.10664C>G (p.Thr3555Ser) | dbSNP |
4 | g.186603868G>T | CA358976868 | FAT1 | c.10658C>A (p.Thr3553Asn) c.10664C>A (p.Thr3555Asn) | COSMIC |
4 | g.186603869T>A | CA358976869 | FAT1 | c.10657A>T (p.Thr3553Ser) c.10663A>T (p.Thr3555Ser) | dbSNP |
4 | g.186603869T>C | CA358976870 | FAT1 | c.10657A>G (p.Thr3553Ala) c.10663A>G (p.Thr3555Ala) | dbSNP |
4 | g.186603869T>G | CA358976871 | FAT1 | c.10657A>C (p.Thr3553Pro) c.10663A>C (p.Thr3555Pro) | dbSNP |
4 | g.186603870G>A | CA442889173 | FAT1 | c.10656C>T (p.Ile3552=) c.10662C>T (p.Ile3554=) | dbSNP |
4 | g.186603870G>C | CA3165300 | FAT1 | c.10656C>G (p.Ile3552Met) c.10662C>G (p.Ile3554Met) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.186603870G= | CA1520094252 | FAT1 | c.10656C= (p.Ile3552=) c.10662C= (p.Ile3554=) | |
4 | g.186603870G>T | CA442889181 | FAT1 | c.10656C>A (p.Ile3552=) c.10662C>A (p.Ile3554=) | dbSNP |
4 | g.186603871A>C | CA358976872 | FAT1 | c.10655T>G (p.Ile3552Ser) c.10661T>G (p.Ile3554Ser) | |
4 | g.186603871A>G | CA358976874 | FAT1 | c.10655T>C (p.Ile3552Thr) c.10661T>C (p.Ile3554Thr) | dbSNP |
4 | g.186603871A>T | CA358976873 | FAT1 | c.10655T>A (p.Ile3552Asn) c.10661T>A (p.Ile3554Asn) | dbSNP |
4 | g.186603872T>A | CA358976875 | FAT1 | c.10654A>T (p.Ile3552Phe) c.10660A>T (p.Ile3554Phe) | dbSNP |
4 | g.186603872T>C | CA358976876 | FAT1 | c.10654A>G (p.Ile3552Val) c.10660A>G (p.Ile3554Val) | dbSNP |
4 | g.186603872T>G | CA358976877 | FAT1 | c.10654A>C (p.Ile3552Leu) c.10660A>C (p.Ile3554Leu) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.186603872T= | CA1520094253 | FAT1 | c.10654A= (p.Ile3552=) c.10660A= (p.Ile3554=) | |
4 | g.186603873G>A | CA442889192 | FAT1 | c.10653C>T (p.Phe3551=) c.10659C>T (p.Phe3553=) | gnomAD v4 |
4 | g.186603873G>C | CA358976879 | FAT1 | c.10653C>G (p.Phe3551Leu) c.10659C>G (p.Phe3553Leu) | dbSNP |
4 | g.186603873G>T | CA358976880 | FAT1 | c.10653C>A (p.Phe3551Leu) c.10659C>A (p.Phe3553Leu) | |
4 | g.186603874A>C | CA358976881 | FAT1 | c.10652T>G (p.Phe3551Cys) c.10658T>G (p.Phe3553Cys) | |
4 | g.186603874A>G | CA358976883 | FAT1 | c.10652T>C (p.Phe3551Ser) c.10658T>C (p.Phe3553Ser) | |
4 | g.186603874A>T | CA358976882 | FAT1 | c.10652T>A (p.Phe3551Tyr) c.10658T>A (p.Phe3553Tyr) | dbSNP |
4 | g.186603875A>C | CA358976884 | FAT1 | c.10651T>G (p.Phe3551Val) c.10657T>G (p.Phe3553Val) | |
4 | g.186603875A>G | CA358976885 | FAT1 | c.10651T>C (p.Phe3551Leu) c.10657T>C (p.Phe3553Leu) | dbSNP |
4 | g.186603875A>T | CA358976886 | FAT1 | c.10651T>A (p.Phe3551Ile) c.10657T>A (p.Phe3553Ile) | dbSNP |
4 | g.186603876A>C | CA358976887 | FAT1 | c.10650T>G (p.Ile3550Met) c.10656T>G (p.Ile3552Met) | gnomAD v4 |
4 | g.186603876A>G | CA442889203 | FAT1 | c.10650T>C (p.Ile3550=) c.10656T>C (p.Ile3552=) | |
4 | g.186603876A>T | CA442889205 | FAT1 | c.10650T>A (p.Ile3550=) c.10656T>A (p.Ile3552=) | |
4 | g.186603877A>C | CA358976888 | FAT1 | c.10649T>G (p.Ile3550Ser) c.10655T>G (p.Ile3552Ser) | dbSNP |
4 | g.186603877A>G | CA358976889 | FAT1 | c.10649T>C (p.Ile3550Thr) c.10655T>C (p.Ile3552Thr) | gnomAD v4 |
4 | g.186603877A>T | CA358976890 | FAT1 | c.10649T>A (p.Ile3550Asn) c.10655T>A (p.Ile3552Asn) | dbSNP |
4 | g.186603878T>A | CA358976891 | FAT1 | c.10648A>T (p.Ile3550Phe) c.10654A>T (p.Ile3552Phe) | dbSNP |
4 | g.186603878T>C | CA358976892 | FAT1 | c.10648A>G (p.Ile3550Val) c.10654A>G (p.Ile3552Val) | |
4 | g.186603878T>G | CA358976893 | FAT1 | c.10648A>C (p.Ile3550Leu) c.10654A>C (p.Ile3552Leu) | |
4 | g.186603879C>A | CA358976894 | FAT1 | c.10647G>T (p.Glu3549Asp) c.10653G>T (p.Glu3551Asp) | dbSNP |
4 | g.186603879C>G | CA358976895 | FAT1 | c.10647G>C (p.Glu3549Asp) c.10653G>C (p.Glu3551Asp) | dbSNP |
4 | g.186603879C>T | CA442889217 | FAT1 | c.10647G>A (p.Glu3549=) c.10653G>A (p.Glu3551=) | |
4 | g.186603880T>A | CA358976896 | FAT1 | c.10646A>T (p.Glu3549Val) c.10652A>T (p.Glu3551Val) | |
4 | g.186603880T>C | CA358976898 | FAT1 | c.10646A>G (p.Glu3549Gly) c.10652A>G (p.Glu3551Gly) | |
4 | g.186603880T>G | CA358976897 | FAT1 | c.10646A>C (p.Glu3549Ala) c.10652A>C (p.Glu3551Ala) |