Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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) | |
4 | g.186603881C>A | CA358976899 | FAT1 | c.10645G>T (p.Glu3549Ter) c.10651G>T (p.Glu3551Ter) | dbSNP |
4 | g.186603881C>G | CA358976900 | FAT1 | c.10645G>C (p.Glu3549Gln) c.10651G>C (p.Glu3551Gln) | dbSNP |
4 | g.186603881C>T | CA358976901 | FAT1 | c.10645G>A (p.Glu3549Lys) c.10651G>A (p.Glu3551Lys) | dbSNP |
4 | g.186603882C>A | CA442889227 | FAT1 | c.10644G>T (p.Leu3548=) c.10650G>T (p.Leu3550=) | dbSNP |
4 | g.186603882C= | CA1520094254 | FAT1 | c.10644G= (p.Leu3548=) c.10650G= (p.Leu3550=) | |
4 | g.186603882C>G | CA442889229 | FAT1 | c.10644G>C (p.Leu3548=) c.10650G>C (p.Leu3550=) | dbSNP |
4 | g.186603882C>T | CA442889234 | FAT1 | c.10644G>A (p.Leu3548=) c.10650G>A (p.Leu3550=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.186603883A>C | CA358976902 | FAT1 | c.10643T>G (p.Leu3548Arg) c.10649T>G (p.Leu3550Arg) | |
4 | g.186603883A>G | CA358976903 | FAT1 | c.10643T>C (p.Leu3548Pro) c.10649T>C (p.Leu3550Pro) | dbSNP |
4 | g.186603883A>T | CA358976904 | FAT1 | c.10643T>A (p.Leu3548Gln) c.10649T>A (p.Leu3550Gln) | dbSNP |
4 | g.186603884G>A | CA442889242 | FAT1 | c.10642C>T (p.Leu3548=) c.10648C>T (p.Leu3550=) | |
4 | g.186603884G>C | CA358976905 | FAT1 | c.10642C>G (p.Leu3548Val) c.10648C>G (p.Leu3550Val) | |
4 | g.186603884G>T | CA358976906 | FAT1 | c.10642C>A (p.Leu3548Met) c.10648C>A (p.Leu3550Met) | |
4 | g.186603887dup | CA2672908288 | FAT1 | c.10642dup (p.Leu3548ProfsTer29) c.10648dup (p.Leu3550ProfsTer29) | gnomAD v4 |
4 | g.186603885G>A | CA442889246 | FAT1 | c.10641C>T (p.Pro3547=) c.10647C>T (p.Pro3549=) | dbSNP gnomAD v4 |
4 | g.186603885G>C | CA112157428 | FAT1 | c.10641C>G (p.Pro3547=) c.10647C>G (p.Pro3549=) | dbSNP |
4 | g.186603885G= | CA1520094255 | FAT1 | c.10641C= (p.Pro3547=) c.10647C= (p.Pro3549=) | |
4 | g.186603885G>T | CA442889249 | FAT1 | c.10641C>A (p.Pro3547=) c.10647C>A (p.Pro3549=) | dbSNP |
4 | g.186603886G>A | CA112157432 | FAT1 | c.10640C>T (p.Pro3547Leu) c.10646C>T (p.Pro3549Leu) | dbSNP gnomAD v4 |
4 | g.186603886G>C | CA358976907 | FAT1 | c.10640C>G (p.Pro3547Arg) c.10646C>G (p.Pro3549Arg) | dbSNP |
4 | g.186603886G= | CA1520094256 | FAT1 | c.10640C= (p.Pro3547=) c.10646C= (p.Pro3549=) | |
4 | g.186603886G>T | CA358976908 | FAT1 | c.10640C>A (p.Pro3547His) c.10646C>A (p.Pro3549His) | dbSNP |
4 | g.186603887G>A | CA358976911 | FAT1 | c.10639C>T (p.Pro3547Ser) c.10645C>T (p.Pro3549Ser) | dbSNP gnomAD v4 |
4 | g.186603887G>C | CA358976910 | FAT1 | c.10639C>G (p.Pro3547Ala) c.10645C>G (p.Pro3549Ala) | dbSNP |
4 | g.186603887G= | CA1520094257 | FAT1 | c.10639C= (p.Pro3547=) c.10645C= (p.Pro3549=) | |
4 | g.186603887G>T | CA358976909 | FAT1 | c.10639C>A (p.Pro3547Thr) c.10645C>A (p.Pro3549Thr) | dbSNP |
4 | g.186603888C>A | CA358976912 | FAT1 | c.10638G>T (p.Leu3546Phe) c.10644G>T (p.Leu3548Phe) | |
4 | g.186603888C= | CA1520094258 | FAT1 | c.10638G= (p.Leu3546=) c.10644G= (p.Leu3548=) | |
4 | g.186603888C>G | CA358976913 | FAT1 | c.10638G>C (p.Leu3546Phe) c.10644G>C (p.Leu3548Phe) | dbSNP |
4 | g.186603888C>T | CA3165301 | FAT1 | c.10638G>A (p.Leu3546=) c.10644G>A (p.Leu3548=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.186603889A>C | CA358976914 | FAT1 | c.10637T>G (p.Leu3546Trp) c.10643T>G (p.Leu3548Trp) | |
4 | g.186603889A>G | CA358976915 | FAT1 | c.10637T>C (p.Leu3546Ser) c.10643T>C (p.Leu3548Ser) | |
4 | g.186603889A>T | CA358976916 | FAT1 | c.10637T>A (p.Leu3546Ter) c.10643T>A (p.Leu3548Ter) | |
4 | g.186603890A>C | CA358976917 | FAT1 | c.10636T>G (p.Leu3546Val) c.10642T>G (p.Leu3548Val) | dbSNP |
4 | g.186603890A>G | CA442889275 | FAT1 | c.10636T>C (p.Leu3546=) c.10642T>C (p.Leu3548=) | |
4 | g.186603890A>T | CA358976918 | FAT1 | c.10636T>A (p.Leu3546Met) c.10642T>A (p.Leu3548Met) | dbSNP |
4 | g.186603891A= | CA1520094259 | FAT1 | c.10635T= (p.Ile3545=) c.10641T= (p.Ile3547=) | |
4 | g.186603891A>C | CA358976919 | FAT1 | c.10635T>G (p.Ile3545Met) c.10641T>G (p.Ile3547Met) | dbSNP |
4 | g.186603891A>G | CA442889282 | FAT1 | c.10635T>C (p.Ile3545=) c.10641T>C (p.Ile3547=) | dbSNP |
4 | g.186603891A>T | CA442889284 | FAT1 | c.10635T>A (p.Ile3545=) c.10641T>A (p.Ile3547=) | |
4 | g.186603892A>C | CA358976920 | FAT1 | c.10634T>G (p.Ile3545Ser) c.10640T>G (p.Ile3547Ser) | dbSNP |
4 | g.186603892A>G | CA358976921 | FAT1 | c.10634T>C (p.Ile3545Thr) c.10640T>C (p.Ile3547Thr) | dbSNP |
4 | g.186603892A>T | CA358976922 | FAT1 | c.10634T>A (p.Ile3545Asn) c.10640T>A (p.Ile3547Asn) | dbSNP |
4 | g.186603893T>A | CA358976923 | FAT1 | c.10633A>T (p.Ile3545Phe) c.10639A>T (p.Ile3547Phe) | dbSNP gnomAD v4 |
4 | g.186603893T>C | CA358976925 | FAT1 | c.10633A>G (p.Ile3545Val) c.10639A>G (p.Ile3547Val) | |
4 | g.186603893T>G | CA358976924 | FAT1 | c.10633A>C (p.Ile3545Leu) c.10639A>C (p.Ile3547Leu) | dbSNP |
4 | g.186603894C>A | CA442889295 | FAT1 | c.10632G>T (p.Ala3544=) c.10638G>T (p.Ala3546=) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.186603894C= | CA1520094260 | FAT1 | c.10632G= (p.Ala3544=) c.10638G= (p.Ala3546=) | |
4 | g.186603894C>G | CA442889299 | FAT1 | c.10632G>C (p.Ala3544=) c.10638G>C (p.Ala3546=) | dbSNP |
4 | g.186603894C>T | CA3165302 | FAT1 | c.10632G>A (p.Ala3544=) c.10638G>A (p.Ala3546=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.186603895G>A | CA358976926 | FAT1 | c.10631C>T (p.Ala3544Val) c.10637C>T (p.Ala3546Val) | dbSNP gnomAD v4 COSMIC COSMIC |
4 | g.186603895G>C | CA358976927 | FAT1 | c.10631C>G (p.Ala3544Gly) c.10637C>G (p.Ala3546Gly) | dbSNP |
4 | g.186603895G= | CA1520094261 | FAT1 | c.10631C= (p.Ala3544=) c.10637C= (p.Ala3546=) | |
4 | g.186603895G>T | CA358976928 | FAT1 | c.10631C>A (p.Ala3544Glu) c.10637C>A (p.Ala3546Glu) | |
4 | g.186603896C>A | CA358976929 | FAT1 | c.10630G>T (p.Ala3544Ser) c.10636G>T (p.Ala3546Ser) | dbSNP |
4 | g.186603896C>G | CA358976930 | FAT1 | c.10630G>C (p.Ala3544Pro) c.10636G>C (p.Ala3546Pro) | dbSNP COSMIC COSMIC |
4 | g.186603896C>T | CA358976931 | FAT1 | c.10630G>A (p.Ala3544Thr) c.10636G>A (p.Ala3546Thr) | dbSNP gnomAD v4 |
4 | g.186603897A>C | CA442887965 | FAT1 | c.10629T>G (p.Pro3543=) c.10635T>G (p.Pro3545=) | |
4 | g.186603897A>G | CA442887968 | FAT1 | c.10629T>C (p.Pro3543=) c.10635T>C (p.Pro3545=) | dbSNP |
4 | g.186603897A>T | CA442887969 | FAT1 | c.10629T>A (p.Pro3543=) c.10635T>A (p.Pro3545=) | dbSNP gnomAD v4 |
4 | g.186603898G>A | CA358976932 | FAT1 | c.10628C>T (p.Pro3543Leu) c.10634C>T (p.Pro3545Leu) | dbSNP |
4 | g.186603898G>C | CA358976934 | FAT1 | c.10628C>G (p.Pro3543Arg) c.10634C>G (p.Pro3545Arg) | dbSNP |
4 | g.186603898G>T | CA358976933 | FAT1 | c.10628C>A (p.Pro3543His) c.10634C>A (p.Pro3545His) | gnomAD v4 |
4 | g.186603899G>A | CA358976935 | FAT1 | c.10627C>T (p.Pro3543Ser) c.10633C>T (p.Pro3545Ser) | |
4 | g.186603899G>C | CA358976936 | FAT1 | c.10627C>G (p.Pro3543Ala) c.10633C>G (p.Pro3545Ala) | |
4 | g.186603899G>T | CA358976937 | FAT1 | c.10627C>A (p.Pro3543Thr) c.10633C>A (p.Pro3545Thr) | |
4 | g.186603900C>A | CA442887988 | FAT1 | c.10626G>T (p.Pro3542=) c.10632G>T (p.Pro3544=) | dbSNP |
4 | g.186603900C= | CA1520094262 | FAT1 | c.10626G= (p.Pro3542=) c.10632G= (p.Pro3544=) | |
4 | g.186603900C>G | CA442887991 | FAT1 | c.10626G>C (p.Pro3542=) c.10632G>C (p.Pro3544=) | |
4 | g.186603900C>T | CA3165303 | FAT1 | c.10626G>A (p.Pro3542=) c.10632G>A (p.Pro3544=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.186603901G>A | CA3165304 | FAT1 | c.10625C>T (p.Pro3542Leu) c.10631C>T (p.Pro3544Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.186603901G>C | CA358976938 | FAT1 | c.10625C>G (p.Pro3542Arg) c.10631C>G (p.Pro3544Arg) | dbSNP gnomAD v4 |
4 | g.186603901G= | CA1520094263 | FAT1 | c.10625C= (p.Pro3542=) c.10631C= (p.Pro3544=) | |
4 | g.186603901G>T | CA358976939 | FAT1 | c.10625C>A (p.Pro3542Gln) c.10631C>A (p.Pro3544Gln) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.186603902G>A | CA358976940 | FAT1 | c.10624C>T (p.Pro3542Ser) c.10630C>T (p.Pro3544Ser) | dbSNP |
4 | g.186603902G>C | CA358976941 | FAT1 | c.10624C>G (p.Pro3542Ala) c.10630C>G (p.Pro3544Ala) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.186603902G= | CA1520094264 | FAT1 | c.10624C= (p.Pro3542=) c.10630C= (p.Pro3544=) | |
4 | g.186603902G>T | CA3165305 | FAT1 | c.10624C>A (p.Pro3542Thr) c.10630C>A (p.Pro3544Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.186603903A>C | CA358976942 | FAT1 | c.10623T>G (p.Tyr3541Ter) c.10629T>G (p.Tyr3543Ter) | |
4 | g.186603903A>G | CA442888013 | FAT1 | c.10623T>C (p.Tyr3541=) c.10629T>C (p.Tyr3543=) | dbSNP gnomAD v4 |
4 | g.186603903A>T | CA358976943 | FAT1 | c.10623T>A (p.Tyr3541Ter) c.10629T>A (p.Tyr3543Ter) | |
4 | g.186603904T>A | CA358976944 | FAT1 | c.10622A>T (p.Tyr3541Phe) c.10628A>T (p.Tyr3543Phe) | dbSNP gnomAD v4 |
4 | g.186603904T>C | CA3165306 | FAT1 | c.10622A>G (p.Tyr3541Cys) c.10628A>G (p.Tyr3543Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.186603904T>G | CA358976945 | FAT1 | c.10622A>C (p.Tyr3541Ser) c.10628A>C (p.Tyr3543Ser) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.186603904T= | CA1520094265 | FAT1 | c.10622A= (p.Tyr3541=) c.10628A= (p.Tyr3543=) | |
4 | g.186603905A>C | CA358976946 | FAT1 | c.10621T>G (p.Tyr3541Asp) c.10627T>G (p.Tyr3543Asp) | |
4 | g.186603905A>G | CA358976947 | FAT1 | c.10621T>C (p.Tyr3541His) c.10627T>C (p.Tyr3543His) | dbSNP |
4 | g.186603905A>T | CA358976948 | FAT1 | c.10621T>A (p.Tyr3541Asn) c.10627T>A (p.Tyr3543Asn) | dbSNP |
4 | g.186603906G>A | CA442888026 | FAT1 | c.10620C>T (p.Ile3540=) c.10626C>T (p.Ile3542=) | dbSNP |
4 | g.186603906G>C | CA358976949 | FAT1 | c.10620C>G (p.Ile3540Met) c.10626C>G (p.Ile3542Met) | dbSNP |
4 | g.186603906G>T | CA442888032 | FAT1 | c.10620C>A (p.Ile3540=) c.10626C>A (p.Ile3542=) | dbSNP |
4 | g.186603907A>C | CA358976950 | FAT1 | c.10619T>G (p.Ile3540Ser) c.10625T>G (p.Ile3542Ser) | |
4 | g.186603907A>G | CA358976952 | FAT1 | c.10619T>C (p.Ile3540Thr) c.10625T>C (p.Ile3542Thr) | dbSNP gnomAD v4 |
4 | g.186603907A>T | CA358976951 | FAT1 | c.10619T>A (p.Ile3540Asn) c.10625T>A (p.Ile3542Asn) | dbSNP |
4 | g.186603908T>A | CA358976953 | FAT1 | c.10618A>T (p.Ile3540Phe) c.10624A>T (p.Ile3542Phe) | dbSNP |
4 | g.186603908T>C | CA358976954 | FAT1 | c.10618A>G (p.Ile3540Val) c.10624A>G (p.Ile3542Val) | gnomAD v4 |
4 | g.186603908T>G | CA358976955 | FAT1 | c.10618A>C (p.Ile3540Leu) c.10624A>C (p.Ile3542Leu) | dbSNP |
4 | g.186603909G>A | CA442888033 | FAT1 | c.10617C>T (p.Ser3539=) c.10623C>T (p.Ser3541=) | dbSNP gnomAD v4 |
4 | g.186603909G>C | CA358976956 | FAT1 | c.10617C>G (p.Ser3539Arg) c.10623C>G (p.Ser3541Arg) | |
4 | g.186603909G= | CA1520094266 | FAT1 | c.10617C= (p.Ser3539=) c.10623C= (p.Ser3541=) | |
4 | g.186603909G>T | CA358976957 | FAT1 | c.10617C>A (p.Ser3539Arg) c.10623C>A (p.Ser3541Arg) | |
4 | g.186603910C>A | CA358976958 | FAT1 | c.10616G>T (p.Ser3539Ile) c.10622G>T (p.Ser3541Ile) | dbSNP |
4 | g.186603910C>G | CA358976959 | FAT1 | c.10616G>C (p.Ser3539Thr) c.10622G>C (p.Ser3541Thr) | dbSNP |
4 | g.186603910C>T | CA358976960 | FAT1 | c.10616G>A (p.Ser3539Asn) c.10622G>A (p.Ser3541Asn) | dbSNP gnomAD v4 |
4 | g.186603911T>A | CA358976961 | FAT1 | c.10615A>T (p.Ser3539Cys) c.10621A>T (p.Ser3541Cys) | dbSNP |
4 | g.186603911T>C | CA358976962 | FAT1 | c.10615A>G (p.Ser3539Gly) c.10621A>G (p.Ser3541Gly) | |
4 | g.186603911T>G | CA358976963 | FAT1 | c.10615A>C (p.Ser3539Arg) c.10621A>C (p.Ser3541Arg) | |
4 | g.186603911T= | CA1520094267 | FAT1 | c.10615A= (p.Ser3539=) c.10621A= (p.Ser3541=) | |
4 | g.186603912C>A | CA358976964 | FAT1 | c.10614G>T (p.Glu3538Asp) c.10620G>T (p.Glu3540Asp) | COSMIC |
4 | g.186603912C>G | CA358976965 | FAT1 | c.10614G>C (p.Glu3538Asp) c.10620G>C (p.Glu3540Asp) | dbSNP |
4 | g.186603912C>T | CA442888041 | FAT1 | c.10614G>A (p.Glu3538=) c.10620G>A (p.Glu3540=) | dbSNP gnomAD v4 |
4 | g.186603913T>A | CA358976966 | FAT1 | c.10613A>T (p.Glu3538Val) c.10619A>T (p.Glu3540Val) | dbSNP |
4 | g.186603913T>C | CA358976968 | FAT1 | c.10613A>G (p.Glu3538Gly) c.10619A>G (p.Glu3540Gly) | |
4 | g.186603913T>G | CA358976967 | FAT1 | c.10613A>C (p.Glu3538Ala) c.10619A>C (p.Glu3540Ala) | |
4 | g.186603914C>A | CA358976969 | FAT1 | c.10612G>T (p.Glu3538Ter) c.10618G>T (p.Glu3540Ter) | dbSNP |
4 | g.186603914C>G | CA358976970 | FAT1 | c.10612G>C (p.Glu3538Gln) c.10618G>C (p.Glu3540Gln) | dbSNP gnomAD v4 |
4 | g.186603914C>T | CA358976971 | FAT1 | c.10612G>A (p.Glu3538Lys) c.10618G>A (p.Glu3540Lys) | dbSNP |
4 | g.186603915C>A | CA358976972 | FAT1 | c.10611G>T (p.Glu3537Asp) c.10617G>T (p.Glu3539Asp) | dbSNP |
4 | g.186603915C>G | CA358976973 | FAT1 | c.10611G>C (p.Glu3537Asp) c.10617G>C (p.Glu3539Asp) | dbSNP |
4 | g.186603915C>T | CA442888066 | FAT1 | c.10611G>A (p.Glu3537=) c.10617G>A (p.Glu3539=) | dbSNP |
4 | g.186603916T>A | CA358976974 | FAT1 | c.10610A>T (p.Glu3537Val) c.10616A>T (p.Glu3539Val) | dbSNP |
4 | g.186603916T>C | CA358976975 | FAT1 | c.10610A>G (p.Glu3537Gly) c.10616A>G (p.Glu3539Gly) | dbSNP |
4 | g.186603916T>G | CA358976976 | FAT1 | c.10610A>C (p.Glu3537Ala) c.10616A>C (p.Glu3539Ala) | |
4 | g.186603917C>A | CA358976977 | FAT1 | c.10609G>T (p.Glu3537Ter) c.10615G>T (p.Glu3539Ter) | dbSNP |
4 | g.186603917C>G | CA358976978 | FAT1 | c.10609G>C (p.Glu3537Gln) c.10615G>C (p.Glu3539Gln) | dbSNP |
4 | g.186603917C>T | CA358976979 | FAT1 | c.10609G>A (p.Glu3537Lys) c.10615G>A (p.Glu3539Lys) | dbSNP gnomAD v4 |
4 | g.186603918A= | CA1520094268 | FAT1 | c.10608T= (p.Ile3536=) c.10614T= (p.Ile3538=) | |
4 | g.186603918A>C | CA358976980 | FAT1 | c.10608T>G (p.Ile3536Met) c.10614T>G (p.Ile3538Met) | dbSNP |
4 | g.186603918A>G | CA442888086 | FAT1 | c.10608T>C (p.Ile3536=) c.10614T>C (p.Ile3538=) | dbSNP |
4 | g.186603918A>T | CA3165307 | FAT1 | c.10608T>A (p.Ile3536=) c.10614T>A (p.Ile3538=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.186603919A>C | CA358976981 | FAT1 | c.10607T>G (p.Ile3536Ser) c.10613T>G (p.Ile3538Ser) | |
4 | g.186603919A>G | CA358976983 | FAT1 | c.10607T>C (p.Ile3536Thr) c.10613T>C (p.Ile3538Thr) | |
4 | g.186603919A>T | CA358976982 | FAT1 | c.10607T>A (p.Ile3536Asn) c.10613T>A (p.Ile3538Asn) | |
4 | g.186603920T>A | CA358976984 | FAT1 | c.10606A>T (p.Ile3536Phe) c.10612A>T (p.Ile3538Phe) | dbSNP |
4 | g.186603920T>C | CA358976986 | FAT1 | c.10606A>G (p.Ile3536Val) c.10612A>G (p.Ile3538Val) | |
4 | g.186603920T>G | CA358976985 | FAT1 | c.10606A>C (p.Ile3536Leu) c.10612A>C (p.Ile3538Leu) | |
4 | g.186603921T>A | CA442888102 | FAT1 | c.10605A>T (p.Val3535=) c.10611A>T (p.Val3537=) | dbSNP gnomAD v4 |
4 | g.186603921T>C | CA442888103 | FAT1 | c.10605A>G (p.Val3535=) c.10611A>G (p.Val3537=) | dbSNP gnomAD v4 |
4 | g.186603921T>G | CA442888106 | FAT1 | c.10605A>C (p.Val3535=) c.10611A>C (p.Val3537=) | dbSNP |
4 | g.186603921T= | CA1520094269 | FAT1 | c.10605A= (p.Val3535=) c.10611A= (p.Val3537=) | |
4 | g.186603922A>C | CA358976987 | FAT1 | c.10604T>G (p.Val3535Gly) c.10610T>G (p.Val3537Gly) | |
4 | g.186603922A>G | CA358976988 | FAT1 | c.10604T>C (p.Val3535Ala) c.10610T>C (p.Val3537Ala) | |
4 | g.186603922A>T | CA358976989 | FAT1 | c.10604T>A (p.Val3535Glu) c.10610T>A (p.Val3537Glu) | |
4 | g.186603923C>A | CA358976990 | FAT1 | c.10603G>T (p.Val3535Leu) c.10609G>T (p.Val3537Leu) | dbSNP |
4 | g.186603923C= | CA1520094270 | FAT1 | c.10603G= (p.Val3535=) c.10609G= (p.Val3537=) | |
4 | g.186603923C>G | CA358976991 | FAT1 | c.10603G>C (p.Val3535Leu) c.10609G>C (p.Val3537Leu) | dbSNP |
4 | g.186603923C>T | CA3165308 | FAT1 | c.10603G>A (p.Val3535Ile) c.10609G>A (p.Val3537Ile) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.186603924C>A | CA358976992 | FAT1 | c.10602G>T (p.Arg3534Ser) c.10608G>T (p.Arg3536Ser) | dbSNP |
4 | g.186603924C>G | CA358976993 | FAT1 | c.10602G>C (p.Arg3534Ser) c.10608G>C (p.Arg3536Ser) | dbSNP |
4 | g.186603924C>T | CA442888119 | FAT1 | c.10602G>A (p.Arg3534=) c.10608G>A (p.Arg3536=) | dbSNP |
4 | g.186603925C>A | CA358976994 | FAT1 | c.10601G>T (p.Arg3534Met) c.10607G>T (p.Arg3536Met) | |
4 | g.186603925C= | CA1520094271 | FAT1 | c.10601G= (p.Arg3534=) c.10607G= (p.Arg3536=) | |
4 | g.186603925C>G | CA358976995 | FAT1 | c.10601G>C (p.Arg3534Thr) c.10607G>C (p.Arg3536Thr) | |
4 | g.186603925C>T | CA112157443 | FAT1 | c.10601G>A (p.Arg3534Lys) c.10607G>A (p.Arg3536Lys) | dbSNP |
4 | g.186603926T>A | CA358976996 | FAT1 | c.10600A>T (p.Arg3534Trp) c.10606A>T (p.Arg3536Trp) | |
4 | g.186603926T>C | CA358976997 | FAT1 | c.10600A>G (p.Arg3534Gly) c.10606A>G (p.Arg3536Gly) | dbSNP |
4 | g.186603926T>G | CA442888132 | FAT1 | c.10600A>C (p.Arg3534=) c.10606A>C (p.Arg3536=) | |
4 | g.186603927A= | CA1520094272 | FAT1 | c.10599T= (p.Ile3533=) c.10605T= (p.Ile3535=) | |
4 | g.186603927A>C | CA358976998 | FAT1 | c.10599T>G (p.Ile3533Met) c.10605T>G (p.Ile3535Met) | |
4 | g.186603927A>G | CA3165309 | FAT1 | c.10599T>C (p.Ile3533=) c.10605T>C (p.Ile3535=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.186603927A>T | CA442888137 | FAT1 | c.10599T>A (p.Ile3533=) c.10605T>A (p.Ile3535=) | |
4 | g.186603928A>C | CA358976999 | FAT1 | c.10598T>G (p.Ile3533Ser) c.10604T>G (p.Ile3535Ser) | |
4 | g.186603928A>G | CA358977000 | FAT1 | c.10598T>C (p.Ile3533Thr) c.10604T>C (p.Ile3535Thr) | gnomAD v4 |
4 | g.186603928A>T | CA358977001 | FAT1 | c.10598T>A (p.Ile3533Asn) c.10604T>A (p.Ile3535Asn) | dbSNP gnomAD v4 |
4 | g.186603929T>A | CA358977002 | FAT1 | c.10597A>T (p.Ile3533Phe) c.10603A>T (p.Ile3535Phe) | dbSNP |
4 | g.186603929T>C | CA3165310 | FAT1 | c.10597A>G (p.Ile3533Val) c.10603A>G (p.Ile3535Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.186603929T>G | CA358977003 | FAT1 | c.10597A>C (p.Ile3533Leu) c.10603A>C (p.Ile3535Leu) | gnomAD v4 |
4 | g.186603929T= | CA1520094273 | FAT1 | c.10597A= (p.Ile3533=) c.10603A= (p.Ile3535=) | |
4 | g.186603930G>A | CA442888160 | FAT1 | c.10596C>T (p.Asp3532=) c.10602C>T (p.Asp3534=) | dbSNP gnomAD v4 |
4 | g.186603930G>C | CA358977004 | FAT1 | c.10596C>G (p.Asp3532Glu) c.10602C>G (p.Asp3534Glu) | dbSNP |
4 | g.186603930G>T | CA358977005 | FAT1 | c.10596C>A (p.Asp3532Glu) c.10602C>A (p.Asp3534Glu) | |
4 | g.186603931T>A | CA358977006 | FAT1 | c.10595A>T (p.Asp3532Val) c.10601A>T (p.Asp3534Val) | dbSNP |
4 | g.186603931T>C | CA358977007 | FAT1 | c.10595A>G (p.Asp3532Gly) c.10601A>G (p.Asp3534Gly) | gnomAD v4 |
4 | g.186603931T>G | CA358977008 | FAT1 | c.10595A>C (p.Asp3532Ala) c.10601A>C (p.Asp3534Ala) | |
4 | g.186603932C>A | CA358977011 | FAT1 | c.10594G>T (p.Asp3532Tyr) c.10600G>T (p.Asp3534Tyr) | dbSNP |
4 | g.186603932C>G | CA358977010 | FAT1 | c.10594G>C (p.Asp3532His) c.10600G>C (p.Asp3534His) | dbSNP |
4 | g.186603932C>T | CA358977009 | FAT1 | c.10594G>A (p.Asp3532Asn) c.10600G>A (p.Asp3534Asn) | dbSNP |
4 | g.186603933A>C | CA358977012 | FAT1 | c.10593T>G (p.Ile3531Met) c.10599T>G (p.Ile3533Met) | |
4 | g.186603933A>G | CA442888166 | FAT1 | c.10593T>C (p.Ile3531=) c.10599T>C (p.Ile3533=) | dbSNP gnomAD v4 |
4 | g.186603933A>T | CA442888167 | FAT1 | c.10593T>A (p.Ile3531=) c.10599T>A (p.Ile3533=) | |
4 | g.186603934A>C | CA358977013 | FAT1 | c.10592T>G (p.Ile3531Ser) c.10598T>G (p.Ile3533Ser) | |
4 | g.186603934A>G | CA358977014 | FAT1 | c.10592T>C (p.Ile3531Thr) c.10598T>C (p.Ile3533Thr) | |
4 | g.186603934A>T | CA358977015 | FAT1 | c.10592T>A (p.Ile3531Asn) c.10598T>A (p.Ile3533Asn) | |
4 | g.186603935T>A | CA358977016 | FAT1 | c.10591A>T (p.Ile3531Phe) c.10597A>T (p.Ile3533Phe) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.186603935T>C | CA3165311 | FAT1 | c.10591A>G (p.Ile3531Val) c.10597A>G (p.Ile3533Val) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.186603935T>G | CA358977017 | FAT1 | c.10591A>C (p.Ile3531Leu) c.10597A>C (p.Ile3533Leu) | |
4 | g.186603935T= | CA1520094274 | FAT1 | c.10591A= (p.Ile3531=) c.10597A= (p.Ile3533=) | |
4 | g.186603936G>A | CA3165312 | FAT1 | c.10590C>T (p.Tyr3530=) c.10596C>T (p.Tyr3532=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.186603936G>C | CA358977018 | FAT1 | c.10590C>G (p.Tyr3530Ter) c.10596C>G (p.Tyr3532Ter) | ClinVar dbSNP |
4 | g.186603936G= | CA1520094275 | FAT1 | c.10590C= (p.Tyr3530=) c.10596C= (p.Tyr3532=) | |
4 | g.186603936G>T | CA358977019 | FAT1 | c.10590C>A (p.Tyr3530Ter) c.10596C>A (p.Tyr3532Ter) | |
4 | g.186603937T>A | CA358977020 | FAT1 | c.10589A>T (p.Tyr3530Phe) c.10595A>T (p.Tyr3532Phe) | dbSNP |
4 | g.186603937T>C | CA358977021 | FAT1 | c.10589A>G (p.Tyr3530Cys) c.10595A>G (p.Tyr3532Cys) | dbSNP |
4 | g.186603937T>G | CA358977022 | FAT1 | c.10589A>C (p.Tyr3530Ser) c.10595A>C (p.Tyr3532Ser) | |
4 | g.186603937dup | CA917387971 | FAT1 | c.10589dup (p.Tyr3530Ter) c.10595dup (p.Tyr3532Ter) | dbSNP |
4 | g.186603938A>C | CA358977025 | FAT1 | c.10588T>G (p.Tyr3530Asp) c.10594T>G (p.Tyr3532Asp) | |
4 | g.186603938A>G | CA358977023 | FAT1 | c.10588T>C (p.Tyr3530His) c.10594T>C (p.Tyr3532His) | dbSNP |
4 | g.186603938A>T | CA358977024 | FAT1 | c.10588T>A (p.Tyr3530Asn) c.10594T>A (p.Tyr3532Asn) | dbSNP |
4 | g.186603939T>A | CA442888185 | FAT1 | c.10587A>T (p.Thr3529=) c.10593A>T (p.Thr3531=) | dbSNP |
4 | g.186603939T>C | CA3165313 | FAT1 | c.10587A>G (p.Thr3529=) c.10593A>G (p.Thr3531=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.186603939T>G | CA442888184 | FAT1 | c.10587A>C (p.Thr3529=) c.10593A>C (p.Thr3531=) | |
4 | g.186603939T= | CA1520094276 | FAT1 | c.10587A= (p.Thr3529=) c.10593A= (p.Thr3531=) | |
4 | g.186603940G>A | CA358977026 | FAT1 | c.10586C>T (p.Thr3529Ile) c.10592C>T (p.Thr3531Ile) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.186603940G>C | CA358977027 | FAT1 | c.10586C>G (p.Thr3529Arg) c.10592C>G (p.Thr3531Arg) | dbSNP |
4 | g.186603940G= | CA1520094277 | FAT1 | c.10586C= (p.Thr3529=) c.10592C= (p.Thr3531=) | |
4 | g.186603940G>T | CA358977028 | FAT1 | c.10586C>A (p.Thr3529Lys) c.10592C>A (p.Thr3531Lys) | |
4 | g.186603941T>A | CA358977029 | FAT1 | c.10585A>T (p.Thr3529Ser) c.10591A>T (p.Thr3531Ser) | dbSNP |
4 | g.186603941T>C | CA3165314 | FAT1 | c.10585A>G (p.Thr3529Ala) c.10591A>G (p.Thr3531Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.186603941T>G | CA358977030 | FAT1 | c.10585A>C (p.Thr3529Pro) c.10591A>C (p.Thr3531Pro) | dbSNP |
4 | g.186603941T= | CA1520094278 | FAT1 | c.10585A= (p.Thr3529=) c.10591A= (p.Thr3531=) | |
4 | g.186603942C>A | CA358977031 | FAT1 | c.10584G>T (p.Leu3528Phe) c.10590G>T (p.Leu3530Phe) | dbSNP gnomAD v4 |
4 | g.186603942C= | CA1520094279 | FAT1 | c.10584G= (p.Leu3528=) c.10590G= (p.Leu3530=) | |
4 | g.186603942C>G | CA358977032 | FAT1 | c.10584G>C (p.Leu3528Phe) c.10590G>C (p.Leu3530Phe) | dbSNP |
4 | g.186603942C>T | CA442888195 | FAT1 | c.10584G>A (p.Leu3528=) c.10590G>A (p.Leu3530=) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.186603943A>C | CA358977033 | FAT1 | c.10583T>G (p.Leu3528Trp) c.10589T>G (p.Leu3530Trp) | |
4 | g.186603943A>G | CA358977034 | FAT1 | c.10583T>C (p.Leu3528Ser) c.10589T>C (p.Leu3530Ser) | dbSNP |
4 | g.186603943A>T | CA358977035 | FAT1 | c.10583T>A (p.Leu3528Ter) c.10589T>A (p.Leu3530Ter) | |
4 | g.186603944A>C | CA358977037 | FAT1 | c.10582T>G (p.Leu3528Val) c.10588T>G (p.Leu3530Val) | |
4 | g.186603944A>G | CA442888207 | FAT1 | c.10582T>C (p.Leu3528=) c.10588T>C (p.Leu3530=) | dbSNP |
4 | g.186603944A>T | CA358977036 | FAT1 | c.10582T>A (p.Leu3528Met) c.10588T>A (p.Leu3530Met) | |
4 | g.186603945A= | CA1520094280 | FAT1 | c.10581T= (p.Ser3527=) c.10587T= (p.Ser3529=) | |
4 | g.186603945A>C | CA442888212 | FAT1 | c.10581T>G (p.Ser3527=) c.10587T>G (p.Ser3529=) | |
4 | g.186603945A>G | CA3165315 | FAT1 | c.10581T>C (p.Ser3527=) c.10587T>C (p.Ser3529=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.186603945A>T | CA442888214 | FAT1 | c.10581T>A (p.Ser3527=) c.10587T>A (p.Ser3529=) | dbSNP |
4 | g.186603946G>A | CA358977038 | FAT1 | c.10580C>T (p.Ser3527Phe) c.10586C>T (p.Ser3529Phe) | dbSNP |
4 | g.186603946G>C | CA358977039 | FAT1 | c.10580C>G (p.Ser3527Cys) c.10586C>G (p.Ser3529Cys) | dbSNP |
4 | g.186603946G>T | CA358977040 | FAT1 | c.10580C>A (p.Ser3527Tyr) c.10586C>A (p.Ser3529Tyr) | |
4 | g.186603947A= | CA1520094281 | FAT1 | c.10579T= (p.Ser3527=) c.10585T= (p.Ser3529=) | |
4 | g.186603947A>C | CA3165316 | FAT1 | c.10579T>G (p.Ser3527Ala) c.10585T>G (p.Ser3529Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.186603947A>G | CA358977041 | FAT1 | c.10579T>C (p.Ser3527Pro) c.10585T>C (p.Ser3529Pro) | dbSNP |
4 | g.186603947A>T | CA358977042 | FAT1 | c.10579T>A (p.Ser3527Thr) c.10585T>A (p.Ser3529Thr) | dbSNP |
4 | g.186603948T>A | CA442888228 | FAT1 | c.10578A>T (p.Ser3526=) c.10584A>T (p.Ser3528=) | dbSNP |
4 | g.186603948T>C | CA442888233 | FAT1 | c.10578A>G (p.Ser3526=) c.10584A>G (p.Ser3528=) | |
4 | g.186603948T>G | CA442888235 | FAT1 | c.10578A>C (p.Ser3526=) c.10584A>C (p.Ser3528=) | |
4 | g.186603949G>A | CA358977045 | FAT1 | c.10577C>T (p.Ser3526Leu) c.10583C>T (p.Ser3528Leu) | dbSNP |
4 | g.186603949G>C | CA358977043 | FAT1 | c.10577C>G (p.Ser3526Ter) c.10583C>G (p.Ser3528Ter) | dbSNP |
4 | g.186603949G>T | CA358977044 | FAT1 | c.10577C>A (p.Ser3526Ter) c.10583C>A (p.Ser3528Ter) | gnomAD v4 |
4 | g.186603949_186603950insGGAAGTTC | CA2523064121 | FAT1 | c.10576_10577insGAACTTCC (p.Ser3526Ter) c.10582_10583insGAACTTCC (p.Ser3528Ter) | |
4 | g.186603950A= | CA1520094282 | FAT1 | c.10576T= (p.Ser3526=) c.10582T= (p.Ser3528=) | |
4 | g.186603950A>C | CA358977046 | FAT1 | c.10576T>G (p.Ser3526Ala) c.10582T>G (p.Ser3528Ala) | dbSNP |
4 | g.186603950A>G | CA358977047 | FAT1 | c.10576T>C (p.Ser3526Pro) c.10582T>C (p.Ser3528Pro) | ClinVar dbSNP COSMIC COSMIC |
4 | g.186603950A>T | CA358977048 | FAT1 | c.10576T>A (p.Ser3526Thr) c.10582T>A (p.Ser3528Thr) | dbSNP |
4 | g.186603951C>A | CA358977049 | FAT1 | c.10575G>T (p.Leu3525Phe) c.10581G>T (p.Leu3527Phe) | dbSNP gnomAD v4 |
4 | g.186603951C>G | CA358977050 | FAT1 | c.10575G>C (p.Leu3525Phe) c.10581G>C (p.Leu3527Phe) | dbSNP |
4 | g.186603951C>T | CA442888244 | FAT1 | c.10575G>A (p.Leu3525=) c.10581G>A (p.Leu3527=) | dbSNP |
4 | g.186603952A>C | CA358977053 | FAT1 | c.10574T>G (p.Leu3525Trp) c.10580T>G (p.Leu3527Trp) | |
4 | g.186603952A>G | CA358977051 | FAT1 | c.10574T>C (p.Leu3525Ser) c.10580T>C (p.Leu3527Ser) | dbSNP |
4 | g.186603952A>T | CA358977052 | FAT1 | c.10574T>A (p.Leu3525Ter) c.10580T>A (p.Leu3527Ter) | dbSNP |
4 | g.186603953A>C | CA358977054 | FAT1 | c.10573T>G (p.Leu3525Val) c.10579T>G (p.Leu3527Val) | dbSNP |
4 | g.186603953A>G | CA442888253 | FAT1 | c.10573T>C (p.Leu3525=) c.10579T>C (p.Leu3527=) | |
4 | g.186603953A>T | CA358977055 | FAT1 | c.10573T>A (p.Leu3525Met) c.10579T>A (p.Leu3527Met) | dbSNP |
4 | g.186603954C>A | CA358977056 | FAT1 | c.10572G>T (p.Gln3524His) c.10578G>T (p.Gln3526His) | |
4 | g.186603954C= | CA1520094283 | FAT1 | c.10572G= (p.Gln3524=) c.10578G= (p.Gln3526=) | |
4 | g.186603954C>G | CA3165317 | FAT1 | c.10572G>C (p.Gln3524His) c.10578G>C (p.Gln3526His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.186603954C>T | CA442888259 | FAT1 | c.10572G>A (p.Gln3524=) c.10578G>A (p.Gln3526=) | dbSNP |
4 | g.186603955T>A | CA358977057 | FAT1 | c.10571A>T (p.Gln3524Leu) c.10577A>T (p.Gln3526Leu) | dbSNP |
4 | g.186603955T>C | CA358977058 | FAT1 | c.10571A>G (p.Gln3524Arg) c.10577A>G (p.Gln3526Arg) | dbSNP |
4 | g.186603955T>G | CA358977059 | FAT1 | c.10571A>C (p.Gln3524Pro) c.10577A>C (p.Gln3526Pro) | |
4 | g.186603956G>A | CA358977060 | FAT1 | c.10570C>T (p.Gln3524Ter) c.10576C>T (p.Gln3526Ter) | dbSNP COSMIC COSMIC |
4 | g.186603956G>C | CA358977061 | FAT1 | c.10570C>G (p.Gln3524Glu) c.10576C>G (p.Gln3526Glu) | dbSNP |
4 | g.186603956G>T | CA358977062 | FAT1 | c.10570C>A (p.Gln3524Lys) c.10576C>A (p.Gln3526Lys) | |
4 | g.186603957A>C | CA442888265 | FAT1 | c.10569T>G (p.Pro3523=) c.10575T>G (p.Pro3525=) | dbSNP |
4 | g.186603957A>G | CA442888266 | FAT1 | c.10569T>C (p.Pro3523=) c.10575T>C (p.Pro3525=) | dbSNP |
4 | g.186603957A>T | CA442888269 | FAT1 | c.10569T>A (p.Pro3523=) c.10575T>A (p.Pro3525=) | dbSNP |
4 | g.186603958G>A | CA358977063 | FAT1 | c.10568C>T (p.Pro3523Leu) c.10574C>T (p.Pro3525Leu) | dbSNP |
4 | g.186603958G>C | CA358977064 | FAT1 | c.10568C>G (p.Pro3523Arg) c.10574C>G (p.Pro3525Arg) | dbSNP |
4 | g.186603958G>T | CA358977065 | FAT1 | c.10568C>A (p.Pro3523His) c.10574C>A (p.Pro3525His) | dbSNP |
4 | g.186603959G>A | CA358977066 | FAT1 | c.10567C>T (p.Pro3523Ser) c.10573C>T (p.Pro3525Ser) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.186603959G>C | CA358977068 | FAT1 | c.10567C>G (p.Pro3523Ala) c.10573C>G (p.Pro3525Ala) | dbSNP |
4 | g.186603959G= | CA1520094284 | FAT1 | c.10567C= (p.Pro3523=) c.10573C= (p.Pro3525=) | |
4 | g.186603959G>T | CA358977067 | FAT1 | c.10567C>A (p.Pro3523Thr) c.10573C>A (p.Pro3525Thr) | |
4 | g.186603960C>A | CA358977069 | FAT1 | c.10566G>T (p.Lys3522Asn) c.10572G>T (p.Lys3524Asn) | dbSNP |
4 | g.186603960C= | CA1520094285 | FAT1 | c.10566G= (p.Lys3522=) c.10572G= (p.Lys3524=) | |
4 | g.186603960C>G | CA358977070 | FAT1 | c.10566G>C (p.Lys3522Asn) c.10572G>C (p.Lys3524Asn) | dbSNP |
4 | g.186603960C>T | CA442888282 | FAT1 | c.10566G>A (p.Lys3522=) c.10572G>A (p.Lys3524=) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.186603961T>A | CA358977071 | FAT1 | c.10565A>T (p.Lys3522Met) c.10571A>T (p.Lys3524Met) | dbSNP |
4 | g.186603961T>C | CA358977072 | FAT1 | c.10565A>G (p.Lys3522Arg) c.10571A>G (p.Lys3524Arg) | dbSNP |
4 | g.186603961T>G | CA358977073 | FAT1 | c.10565A>C (p.Lys3522Thr) c.10571A>C (p.Lys3524Thr) | |
4 | g.186603962T>A | CA358977074 | FAT1 | c.10564A>T (p.Lys3522Ter) c.10570A>T (p.Lys3524Ter) | |
4 | g.186603962T>C | CA358977075 | FAT1 | c.10564A>G (p.Lys3522Glu) c.10570A>G (p.Lys3524Glu) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.186603962T>G | CA358977076 | FAT1 | c.10564A>C (p.Lys3522Gln) c.10570A>C (p.Lys3524Gln) | |
4 | g.186603962T= | CA1520094286 | FAT1 | c.10564A= (p.Lys3522=) c.10570A= (p.Lys3524=) | |
4 | g.186603963T>A | CA442888296 | FAT1 | c.10563A>T (p.Gly3521=) c.10569A>T (p.Gly3523=) | |
4 | g.186603963T>C | CA442888298 | FAT1 | c.10563A>G (p.Gly3521=) c.10569A>G (p.Gly3523=) | |
4 | g.186603963T>G | CA442888300 | FAT1 | c.10563A>C (p.Gly3521=) c.10569A>C (p.Gly3523=) | |
4 | g.186603964C>A | CA358977077 | FAT1 | c.10562G>T (p.Gly3521Val) c.10568G>T (p.Gly3523Val) | dbSNP |
4 | g.186603964C>G | CA358977078 | FAT1 | c.10562G>C (p.Gly3521Ala) c.10568G>C (p.Gly3523Ala) | dbSNP |
4 | g.186603964C>T | CA358977079 | FAT1 | c.10562G>A (p.Gly3521Glu) c.10568G>A (p.Gly3523Glu) | dbSNP |
4 | g.186603965C>A | CA358977080 | FAT1 | c.10561G>T (p.Gly3521Ter) c.10567G>T (p.Gly3523Ter) | dbSNP COSMIC COSMIC |
4 | g.186603965C>G | CA358977081 | FAT1 | c.10561G>C (p.Gly3521Arg) c.10567G>C (p.Gly3523Arg) | dbSNP |
4 | g.186603965C>T | CA358977082 | FAT1 | c.10561G>A (p.Gly3521Arg) c.10567G>A (p.Gly3523Arg) | dbSNP |
4 | g.186603966A>C | CA358977083 | FAT1 | c.10560T>G (p.Asn3520Lys) c.10566T>G (p.Asn3522Lys) | |
4 | g.186603966A>G | CA442888308 | FAT1 | c.10560T>C (p.Asn3520=) c.10566T>C (p.Asn3522=) | |
4 | g.186603966A>T | CA358977084 | FAT1 | c.10560T>A (p.Asn3520Lys) c.10566T>A (p.Asn3522Lys) | |
4 | g.186603967T>A | CA358977085 | FAT1 | c.10559A>T (p.Asn3520Ile) c.10565A>T (p.Asn3522Ile) | dbSNP |
4 | g.186603967T>C | CA358977086 | FAT1 | c.10559A>G (p.Asn3520Ser) c.10565A>G (p.Asn3522Ser) | |
4 | g.186603967T>G | CA358977087 | FAT1 | c.10559A>C (p.Asn3520Thr) c.10565A>C (p.Asn3522Thr) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.186603967T= | CA1520094287 | FAT1 | c.10559A= (p.Asn3520=) c.10565A= (p.Asn3522=) | |
4 | g.186603968T>A | CA358977088 | FAT1 | c.10558A>T (p.Asn3520Tyr) c.10564A>T (p.Asn3522Tyr) | dbSNP |
4 | g.186603968T>C | CA358977089 | FAT1 | c.10558A>G (p.Asn3520Asp) c.10564A>G (p.Asn3522Asp) | |
4 | g.186603968T>G | CA3165318 | FAT1 | c.10558A>C (p.Asn3520His) c.10564A>C (p.Asn3522His) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.186603968T= | CA1520094288 | FAT1 | c.10558A= (p.Asn3520=) c.10564A= (p.Asn3522=) | |
4 | g.186603969A= | CA1520094289 | FAT1 | c.10557T= (p.Asp3519=) c.10563T= (p.Asp3521=) | |
4 | g.186603969A>C | CA358977090 | FAT1 | c.10557T>G (p.Asp3519Glu) c.10563T>G (p.Asp3521Glu) | dbSNP |
4 | g.186603969A>G | CA3165319 | FAT1 | c.10557T>C (p.Asp3519=) c.10563T>C (p.Asp3521=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.186603969A>T | CA358977091 | FAT1 | c.10557T>A (p.Asp3519Glu) c.10563T>A (p.Asp3521Glu) | dbSNP |
4 | g.186603970T>A | CA358977092 | FAT1 | c.10556A>T (p.Asp3519Val) c.10562A>T (p.Asp3521Val) | dbSNP |
4 | g.186603970T>C | CA358977093 | FAT1 | c.10556A>G (p.Asp3519Gly) c.10562A>G (p.Asp3521Gly) | gnomAD v4 |
4 | g.186603970T>G | CA358977094 | FAT1 | c.10556A>C (p.Asp3519Ala) c.10562A>C (p.Asp3521Ala) | |
4 | g.186603971C>A | CA358977095 | FAT1 | c.10555G>T (p.Asp3519Tyr) c.10561G>T (p.Asp3521Tyr) | dbSNP |
4 | g.186603971C= | CA1520094290 | FAT1 | c.10555G= (p.Asp3519=) c.10561G= (p.Asp3521=) | |
4 | g.186603971C>G | CA358977097 | FAT1 | c.10555G>C (p.Asp3519His) c.10561G>C (p.Asp3521His) | dbSNP |
4 | g.186603971C>T | CA358977096 | FAT1 | c.10555G>A (p.Asp3519Asn) c.10561G>A (p.Asp3521Asn) | dbSNP |
4 | g.186603972T>A | CA442888327 | FAT1 | c.10554A>T (p.Ala3518=) c.10560A>T (p.Ala3520=) | dbSNP |
4 | g.186603972T>C | CA442888329 | FAT1 | c.10554A>G (p.Ala3518=) c.10560A>G (p.Ala3520=) | gnomAD v4 |
4 | g.186603972T>G | CA442888330 | FAT1 | c.10554A>C (p.Ala3518=) c.10560A>C (p.Ala3520=) | |
4 | g.186603973G>A | CA358977098 | FAT1 | c.10553C>T (p.Ala3518Val) c.10559C>T (p.Ala3520Val) | gnomAD v4 |
4 | g.186603973G>C | CA358977101 | FAT1 | c.10553C>G (p.Ala3518Gly) c.10559C>G (p.Ala3520Gly) | |
4 | g.186603973G>T | CA358977100 | FAT1 | c.10553C>A (p.Ala3518Glu) c.10559C>A (p.Ala3520Glu) |