Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.186603873G>ACA442889192FAT1c.10653C>T (p.Phe3551=)
c.10659C>T (p.Phe3553=)
gnomAD v4
4g.186603873G>CCA358976879FAT1c.10653C>G (p.Phe3551Leu)
c.10659C>G (p.Phe3553Leu)
dbSNP
4g.186603873G>TCA358976880FAT1c.10653C>A (p.Phe3551Leu)
c.10659C>A (p.Phe3553Leu)
4g.186603874A>CCA358976881FAT1c.10652T>G (p.Phe3551Cys)
c.10658T>G (p.Phe3553Cys)
4g.186603874A>GCA358976883FAT1c.10652T>C (p.Phe3551Ser)
c.10658T>C (p.Phe3553Ser)
4g.186603874A>TCA358976882FAT1c.10652T>A (p.Phe3551Tyr)
c.10658T>A (p.Phe3553Tyr)
dbSNP
4g.186603875A>CCA358976884FAT1c.10651T>G (p.Phe3551Val)
c.10657T>G (p.Phe3553Val)
4g.186603875A>GCA358976885FAT1c.10651T>C (p.Phe3551Leu)
c.10657T>C (p.Phe3553Leu)
dbSNP
4g.186603875A>TCA358976886FAT1c.10651T>A (p.Phe3551Ile)
c.10657T>A (p.Phe3553Ile)
dbSNP
4g.186603876A>CCA358976887FAT1c.10650T>G (p.Ile3550Met)
c.10656T>G (p.Ile3552Met)
gnomAD v4
4g.186603876A>GCA442889203FAT1c.10650T>C (p.Ile3550=)
c.10656T>C (p.Ile3552=)
4g.186603876A>TCA442889205FAT1c.10650T>A (p.Ile3550=)
c.10656T>A (p.Ile3552=)
4g.186603877A>CCA358976888FAT1c.10649T>G (p.Ile3550Ser)
c.10655T>G (p.Ile3552Ser)
dbSNP
4g.186603877A>GCA358976889FAT1c.10649T>C (p.Ile3550Thr)
c.10655T>C (p.Ile3552Thr)
gnomAD v4
4g.186603877A>TCA358976890FAT1c.10649T>A (p.Ile3550Asn)
c.10655T>A (p.Ile3552Asn)
dbSNP
4g.186603878T>ACA358976891FAT1c.10648A>T (p.Ile3550Phe)
c.10654A>T (p.Ile3552Phe)
dbSNP
4g.186603878T>CCA358976892FAT1c.10648A>G (p.Ile3550Val)
c.10654A>G (p.Ile3552Val)
4g.186603878T>GCA358976893FAT1c.10648A>C (p.Ile3550Leu)
c.10654A>C (p.Ile3552Leu)
4g.186603879C>ACA358976894FAT1c.10647G>T (p.Glu3549Asp)
c.10653G>T (p.Glu3551Asp)
dbSNP
4g.186603879C>GCA358976895FAT1c.10647G>C (p.Glu3549Asp)
c.10653G>C (p.Glu3551Asp)
dbSNP
4g.186603879C>TCA442889217FAT1c.10647G>A (p.Glu3549=)
c.10653G>A (p.Glu3551=)
4g.186603880T>ACA358976896FAT1c.10646A>T (p.Glu3549Val)
c.10652A>T (p.Glu3551Val)
4g.186603880T>CCA358976898FAT1c.10646A>G (p.Glu3549Gly)
c.10652A>G (p.Glu3551Gly)
4g.186603880T>GCA358976897FAT1c.10646A>C (p.Glu3549Ala)
c.10652A>C (p.Glu3551Ala)
4g.186603881C>ACA358976899FAT1c.10645G>T (p.Glu3549Ter)
c.10651G>T (p.Glu3551Ter)
dbSNP
4g.186603881C>GCA358976900FAT1c.10645G>C (p.Glu3549Gln)
c.10651G>C (p.Glu3551Gln)
dbSNP
4g.186603881C>TCA358976901FAT1c.10645G>A (p.Glu3549Lys)
c.10651G>A (p.Glu3551Lys)
dbSNP
4g.186603882C>ACA442889227FAT1c.10644G>T (p.Leu3548=)
c.10650G>T (p.Leu3550=)
dbSNP
4g.186603882C=CA1520094254FAT1c.10644G= (p.Leu3548=)
c.10650G= (p.Leu3550=)
4g.186603882C>GCA442889229FAT1c.10644G>C (p.Leu3548=)
c.10650G>C (p.Leu3550=)
dbSNP
4g.186603882C>TCA442889234FAT1c.10644G>A (p.Leu3548=)
c.10650G>A (p.Leu3550=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.186603883A>CCA358976902FAT1c.10643T>G (p.Leu3548Arg)
c.10649T>G (p.Leu3550Arg)
4g.186603883A>GCA358976903FAT1c.10643T>C (p.Leu3548Pro)
c.10649T>C (p.Leu3550Pro)
dbSNP
4g.186603883A>TCA358976904FAT1c.10643T>A (p.Leu3548Gln)
c.10649T>A (p.Leu3550Gln)
dbSNP
4g.186603884G>ACA442889242FAT1c.10642C>T (p.Leu3548=)
c.10648C>T (p.Leu3550=)
4g.186603884G>CCA358976905FAT1c.10642C>G (p.Leu3548Val)
c.10648C>G (p.Leu3550Val)
4g.186603884G>TCA358976906FAT1c.10642C>A (p.Leu3548Met)
c.10648C>A (p.Leu3550Met)
4g.186603887dupCA2672908288FAT1c.10642dup (p.Leu3548ProfsTer29)
c.10648dup (p.Leu3550ProfsTer29)
gnomAD v4
4g.186603885G>ACA442889246FAT1c.10641C>T (p.Pro3547=)
c.10647C>T (p.Pro3549=)
dbSNP gnomAD v4
4g.186603885G>CCA112157428FAT1c.10641C>G (p.Pro3547=)
c.10647C>G (p.Pro3549=)
dbSNP
4g.186603885G=CA1520094255FAT1c.10641C= (p.Pro3547=)
c.10647C= (p.Pro3549=)
4g.186603885G>TCA442889249FAT1c.10641C>A (p.Pro3547=)
c.10647C>A (p.Pro3549=)
dbSNP
4g.186603886G>ACA112157432FAT1c.10640C>T (p.Pro3547Leu)
c.10646C>T (p.Pro3549Leu)
dbSNP gnomAD v4
4g.186603886G>CCA358976907FAT1c.10640C>G (p.Pro3547Arg)
c.10646C>G (p.Pro3549Arg)
dbSNP
4g.186603886G=CA1520094256FAT1c.10640C= (p.Pro3547=)
c.10646C= (p.Pro3549=)
4g.186603886G>TCA358976908FAT1c.10640C>A (p.Pro3547His)
c.10646C>A (p.Pro3549His)
dbSNP
4g.186603887G>ACA358976911FAT1c.10639C>T (p.Pro3547Ser)
c.10645C>T (p.Pro3549Ser)
dbSNP gnomAD v4
4g.186603887G>CCA358976910FAT1c.10639C>G (p.Pro3547Ala)
c.10645C>G (p.Pro3549Ala)
dbSNP
4g.186603887G=CA1520094257FAT1c.10639C= (p.Pro3547=)
c.10645C= (p.Pro3549=)
4g.186603887G>TCA358976909FAT1c.10639C>A (p.Pro3547Thr)
c.10645C>A (p.Pro3549Thr)
dbSNP
4g.186603888C>ACA358976912FAT1c.10638G>T (p.Leu3546Phe)
c.10644G>T (p.Leu3548Phe)
4g.186603888C=CA1520094258FAT1c.10638G= (p.Leu3546=)
c.10644G= (p.Leu3548=)
4g.186603888C>GCA358976913FAT1c.10638G>C (p.Leu3546Phe)
c.10644G>C (p.Leu3548Phe)
dbSNP
4g.186603888C>TCA3165301FAT1c.10638G>A (p.Leu3546=)
c.10644G>A (p.Leu3548=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.186603889A>CCA358976914FAT1c.10637T>G (p.Leu3546Trp)
c.10643T>G (p.Leu3548Trp)
4g.186603889A>GCA358976915FAT1c.10637T>C (p.Leu3546Ser)
c.10643T>C (p.Leu3548Ser)
4g.186603889A>TCA358976916FAT1c.10637T>A (p.Leu3546Ter)
c.10643T>A (p.Leu3548Ter)
4g.186603890A>CCA358976917FAT1c.10636T>G (p.Leu3546Val)
c.10642T>G (p.Leu3548Val)
dbSNP
4g.186603890A>GCA442889275FAT1c.10636T>C (p.Leu3546=)
c.10642T>C (p.Leu3548=)
4g.186603890A>TCA358976918FAT1c.10636T>A (p.Leu3546Met)
c.10642T>A (p.Leu3548Met)
dbSNP
4g.186603891A=CA1520094259FAT1c.10635T= (p.Ile3545=)
c.10641T= (p.Ile3547=)
4g.186603891A>CCA358976919FAT1c.10635T>G (p.Ile3545Met)
c.10641T>G (p.Ile3547Met)
dbSNP
4g.186603891A>GCA442889282FAT1c.10635T>C (p.Ile3545=)
c.10641T>C (p.Ile3547=)
dbSNP
4g.186603891A>TCA442889284FAT1c.10635T>A (p.Ile3545=)
c.10641T>A (p.Ile3547=)
4g.186603892A>CCA358976920FAT1c.10634T>G (p.Ile3545Ser)
c.10640T>G (p.Ile3547Ser)
dbSNP
4g.186603892A>GCA358976921FAT1c.10634T>C (p.Ile3545Thr)
c.10640T>C (p.Ile3547Thr)
dbSNP
4g.186603892A>TCA358976922FAT1c.10634T>A (p.Ile3545Asn)
c.10640T>A (p.Ile3547Asn)
dbSNP
4g.186603893T>ACA358976923FAT1c.10633A>T (p.Ile3545Phe)
c.10639A>T (p.Ile3547Phe)
dbSNP gnomAD v4
4g.186603893T>CCA358976925FAT1c.10633A>G (p.Ile3545Val)
c.10639A>G (p.Ile3547Val)
4g.186603893T>GCA358976924FAT1c.10633A>C (p.Ile3545Leu)
c.10639A>C (p.Ile3547Leu)
dbSNP
4g.186603894C>ACA442889295FAT1c.10632G>T (p.Ala3544=)
c.10638G>T (p.Ala3546=)
dbSNP gnomAD v3 gnomAD v4
4g.186603894C=CA1520094260FAT1c.10632G= (p.Ala3544=)
c.10638G= (p.Ala3546=)
4g.186603894C>GCA442889299FAT1c.10632G>C (p.Ala3544=)
c.10638G>C (p.Ala3546=)
dbSNP
4g.186603894C>TCA3165302FAT1c.10632G>A (p.Ala3544=)
c.10638G>A (p.Ala3546=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.186603895G>ACA358976926FAT1c.10631C>T (p.Ala3544Val)
c.10637C>T (p.Ala3546Val)
dbSNP gnomAD v4 COSMIC COSMIC
4g.186603895G>CCA358976927FAT1c.10631C>G (p.Ala3544Gly)
c.10637C>G (p.Ala3546Gly)
dbSNP
4g.186603895G=CA1520094261FAT1c.10631C= (p.Ala3544=)
c.10637C= (p.Ala3546=)
4g.186603895G>TCA358976928FAT1c.10631C>A (p.Ala3544Glu)
c.10637C>A (p.Ala3546Glu)
4g.186603896C>ACA358976929FAT1c.10630G>T (p.Ala3544Ser)
c.10636G>T (p.Ala3546Ser)
dbSNP
4g.186603896C>GCA358976930FAT1c.10630G>C (p.Ala3544Pro)
c.10636G>C (p.Ala3546Pro)
dbSNP COSMIC COSMIC
4g.186603896C>TCA358976931FAT1c.10630G>A (p.Ala3544Thr)
c.10636G>A (p.Ala3546Thr)
dbSNP gnomAD v4
4g.186603897A>CCA442887965FAT1c.10629T>G (p.Pro3543=)
c.10635T>G (p.Pro3545=)
4g.186603897A>GCA442887968FAT1c.10629T>C (p.Pro3543=)
c.10635T>C (p.Pro3545=)
dbSNP
4g.186603897A>TCA442887969FAT1c.10629T>A (p.Pro3543=)
c.10635T>A (p.Pro3545=)
dbSNP gnomAD v4
4g.186603898G>ACA358976932FAT1c.10628C>T (p.Pro3543Leu)
c.10634C>T (p.Pro3545Leu)
dbSNP
4g.186603898G>CCA358976934FAT1c.10628C>G (p.Pro3543Arg)
c.10634C>G (p.Pro3545Arg)
dbSNP
4g.186603898G>TCA358976933FAT1c.10628C>A (p.Pro3543His)
c.10634C>A (p.Pro3545His)
gnomAD v4
4g.186603899G>ACA358976935FAT1c.10627C>T (p.Pro3543Ser)
c.10633C>T (p.Pro3545Ser)
4g.186603899G>CCA358976936FAT1c.10627C>G (p.Pro3543Ala)
c.10633C>G (p.Pro3545Ala)
4g.186603899G>TCA358976937FAT1c.10627C>A (p.Pro3543Thr)
c.10633C>A (p.Pro3545Thr)
4g.186603900C>ACA442887988FAT1c.10626G>T (p.Pro3542=)
c.10632G>T (p.Pro3544=)
dbSNP
4g.186603900C=CA1520094262FAT1c.10626G= (p.Pro3542=)
c.10632G= (p.Pro3544=)
4g.186603900C>GCA442887991FAT1c.10626G>C (p.Pro3542=)
c.10632G>C (p.Pro3544=)
4g.186603900C>TCA3165303FAT1c.10626G>A (p.Pro3542=)
c.10632G>A (p.Pro3544=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.186603901G>ACA3165304FAT1c.10625C>T (p.Pro3542Leu)
c.10631C>T (p.Pro3544Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.186603901G>CCA358976938FAT1c.10625C>G (p.Pro3542Arg)
c.10631C>G (p.Pro3544Arg)
dbSNP gnomAD v4
4g.186603901G=CA1520094263FAT1c.10625C= (p.Pro3542=)
c.10631C= (p.Pro3544=)
4g.186603901G>TCA358976939FAT1c.10625C>A (p.Pro3542Gln)
c.10631C>A (p.Pro3544Gln)
dbSNP gnomAD v2 gnomAD v4
4g.186603902G>ACA358976940FAT1c.10624C>T (p.Pro3542Ser)
c.10630C>T (p.Pro3544Ser)
dbSNP
4g.186603902G>CCA358976941FAT1c.10624C>G (p.Pro3542Ala)
c.10630C>G (p.Pro3544Ala)
dbSNP gnomAD v3 gnomAD v4
4g.186603902G=CA1520094264FAT1c.10624C= (p.Pro3542=)
c.10630C= (p.Pro3544=)
4g.186603902G>TCA3165305FAT1c.10624C>A (p.Pro3542Thr)
c.10630C>A (p.Pro3544Thr)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.186603903A>CCA358976942FAT1c.10623T>G (p.Tyr3541Ter)
c.10629T>G (p.Tyr3543Ter)
4g.186603903A>GCA442888013FAT1c.10623T>C (p.Tyr3541=)
c.10629T>C (p.Tyr3543=)
dbSNP gnomAD v4
4g.186603903A>TCA358976943FAT1c.10623T>A (p.Tyr3541Ter)
c.10629T>A (p.Tyr3543Ter)
4g.186603904T>ACA358976944FAT1c.10622A>T (p.Tyr3541Phe)
c.10628A>T (p.Tyr3543Phe)
dbSNP gnomAD v4
4g.186603904T>CCA3165306FAT1c.10622A>G (p.Tyr3541Cys)
c.10628A>G (p.Tyr3543Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.186603904T>GCA358976945FAT1c.10622A>C (p.Tyr3541Ser)
c.10628A>C (p.Tyr3543Ser)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.186603904T=CA1520094265FAT1c.10622A= (p.Tyr3541=)
c.10628A= (p.Tyr3543=)
4g.186603905A>CCA358976946FAT1c.10621T>G (p.Tyr3541Asp)
c.10627T>G (p.Tyr3543Asp)
4g.186603905A>GCA358976947FAT1c.10621T>C (p.Tyr3541His)
c.10627T>C (p.Tyr3543His)
dbSNP
4g.186603905A>TCA358976948FAT1c.10621T>A (p.Tyr3541Asn)
c.10627T>A (p.Tyr3543Asn)
dbSNP
4g.186603906G>ACA442888026FAT1c.10620C>T (p.Ile3540=)
c.10626C>T (p.Ile3542=)
dbSNP
4g.186603906G>CCA358976949FAT1c.10620C>G (p.Ile3540Met)
c.10626C>G (p.Ile3542Met)
dbSNP
4g.186603906G>TCA442888032FAT1c.10620C>A (p.Ile3540=)
c.10626C>A (p.Ile3542=)
dbSNP
4g.186603907A>CCA358976950FAT1c.10619T>G (p.Ile3540Ser)
c.10625T>G (p.Ile3542Ser)
4g.186603907A>GCA358976952FAT1c.10619T>C (p.Ile3540Thr)
c.10625T>C (p.Ile3542Thr)
dbSNP gnomAD v4
4g.186603907A>TCA358976951FAT1c.10619T>A (p.Ile3540Asn)
c.10625T>A (p.Ile3542Asn)
dbSNP
4g.186603908T>ACA358976953FAT1c.10618A>T (p.Ile3540Phe)
c.10624A>T (p.Ile3542Phe)
dbSNP
4g.186603908T>CCA358976954FAT1c.10618A>G (p.Ile3540Val)
c.10624A>G (p.Ile3542Val)
gnomAD v4
4g.186603908T>GCA358976955FAT1c.10618A>C (p.Ile3540Leu)
c.10624A>C (p.Ile3542Leu)
dbSNP
4g.186603909G>ACA442888033FAT1c.10617C>T (p.Ser3539=)
c.10623C>T (p.Ser3541=)
dbSNP gnomAD v4
4g.186603909G>CCA358976956FAT1c.10617C>G (p.Ser3539Arg)
c.10623C>G (p.Ser3541Arg)
4g.186603909G=CA1520094266FAT1c.10617C= (p.Ser3539=)
c.10623C= (p.Ser3541=)
4g.186603909G>TCA358976957FAT1c.10617C>A (p.Ser3539Arg)
c.10623C>A (p.Ser3541Arg)
4g.186603910C>ACA358976958FAT1c.10616G>T (p.Ser3539Ile)
c.10622G>T (p.Ser3541Ile)
dbSNP
4g.186603910C>GCA358976959FAT1c.10616G>C (p.Ser3539Thr)
c.10622G>C (p.Ser3541Thr)
dbSNP
4g.186603910C>TCA358976960FAT1c.10616G>A (p.Ser3539Asn)
c.10622G>A (p.Ser3541Asn)
dbSNP gnomAD v4
4g.186603911T>ACA358976961FAT1c.10615A>T (p.Ser3539Cys)
c.10621A>T (p.Ser3541Cys)
dbSNP
4g.186603911T>CCA358976962FAT1c.10615A>G (p.Ser3539Gly)
c.10621A>G (p.Ser3541Gly)
4g.186603911T>GCA358976963FAT1c.10615A>C (p.Ser3539Arg)
c.10621A>C (p.Ser3541Arg)
4g.186603911T=CA1520094267FAT1c.10615A= (p.Ser3539=)
c.10621A= (p.Ser3541=)
4g.186603912C>ACA358976964FAT1c.10614G>T (p.Glu3538Asp)
c.10620G>T (p.Glu3540Asp)
COSMIC
4g.186603912C>GCA358976965FAT1c.10614G>C (p.Glu3538Asp)
c.10620G>C (p.Glu3540Asp)
dbSNP
4g.186603912C>TCA442888041FAT1c.10614G>A (p.Glu3538=)
c.10620G>A (p.Glu3540=)
dbSNP gnomAD v4
4g.186603913T>ACA358976966FAT1c.10613A>T (p.Glu3538Val)
c.10619A>T (p.Glu3540Val)
dbSNP
4g.186603913T>CCA358976968FAT1c.10613A>G (p.Glu3538Gly)
c.10619A>G (p.Glu3540Gly)
4g.186603913T>GCA358976967FAT1c.10613A>C (p.Glu3538Ala)
c.10619A>C (p.Glu3540Ala)
4g.186603914C>ACA358976969FAT1c.10612G>T (p.Glu3538Ter)
c.10618G>T (p.Glu3540Ter)
dbSNP
4g.186603914C>GCA358976970FAT1c.10612G>C (p.Glu3538Gln)
c.10618G>C (p.Glu3540Gln)
dbSNP gnomAD v4
4g.186603914C>TCA358976971FAT1c.10612G>A (p.Glu3538Lys)
c.10618G>A (p.Glu3540Lys)
dbSNP
4g.186603915C>ACA358976972FAT1c.10611G>T (p.Glu3537Asp)
c.10617G>T (p.Glu3539Asp)
dbSNP
4g.186603915C>GCA358976973FAT1c.10611G>C (p.Glu3537Asp)
c.10617G>C (p.Glu3539Asp)
dbSNP
4g.186603915C>TCA442888066FAT1c.10611G>A (p.Glu3537=)
c.10617G>A (p.Glu3539=)
dbSNP
4g.186603916T>ACA358976974FAT1c.10610A>T (p.Glu3537Val)
c.10616A>T (p.Glu3539Val)
dbSNP
4g.186603916T>CCA358976975FAT1c.10610A>G (p.Glu3537Gly)
c.10616A>G (p.Glu3539Gly)
dbSNP
4g.186603916T>GCA358976976FAT1c.10610A>C (p.Glu3537Ala)
c.10616A>C (p.Glu3539Ala)
4g.186603917C>ACA358976977FAT1c.10609G>T (p.Glu3537Ter)
c.10615G>T (p.Glu3539Ter)
dbSNP
4g.186603917C>GCA358976978FAT1c.10609G>C (p.Glu3537Gln)
c.10615G>C (p.Glu3539Gln)
dbSNP
4g.186603917C>TCA358976979FAT1c.10609G>A (p.Glu3537Lys)
c.10615G>A (p.Glu3539Lys)
dbSNP gnomAD v4
4g.186603918A=CA1520094268FAT1c.10608T= (p.Ile3536=)
c.10614T= (p.Ile3538=)
4g.186603918A>CCA358976980FAT1c.10608T>G (p.Ile3536Met)
c.10614T>G (p.Ile3538Met)
dbSNP
4g.186603918A>GCA442888086FAT1c.10608T>C (p.Ile3536=)
c.10614T>C (p.Ile3538=)
dbSNP
4g.186603918A>TCA3165307FAT1c.10608T>A (p.Ile3536=)
c.10614T>A (p.Ile3538=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.186603919A>CCA358976981FAT1c.10607T>G (p.Ile3536Ser)
c.10613T>G (p.Ile3538Ser)
4g.186603919A>GCA358976983FAT1c.10607T>C (p.Ile3536Thr)
c.10613T>C (p.Ile3538Thr)
4g.186603919A>TCA358976982FAT1c.10607T>A (p.Ile3536Asn)
c.10613T>A (p.Ile3538Asn)
4g.186603920T>ACA358976984FAT1c.10606A>T (p.Ile3536Phe)
c.10612A>T (p.Ile3538Phe)
dbSNP
4g.186603920T>CCA358976986FAT1c.10606A>G (p.Ile3536Val)
c.10612A>G (p.Ile3538Val)
4g.186603920T>GCA358976985FAT1c.10606A>C (p.Ile3536Leu)
c.10612A>C (p.Ile3538Leu)
4g.186603921T>ACA442888102FAT1c.10605A>T (p.Val3535=)
c.10611A>T (p.Val3537=)
dbSNP gnomAD v4
4g.186603921T>CCA442888103FAT1c.10605A>G (p.Val3535=)
c.10611A>G (p.Val3537=)
dbSNP gnomAD v4
4g.186603921T>GCA442888106FAT1c.10605A>C (p.Val3535=)
c.10611A>C (p.Val3537=)
dbSNP
4g.186603921T=CA1520094269FAT1c.10605A= (p.Val3535=)
c.10611A= (p.Val3537=)
4g.186603922A>CCA358976987FAT1c.10604T>G (p.Val3535Gly)
c.10610T>G (p.Val3537Gly)
4g.186603922A>GCA358976988FAT1c.10604T>C (p.Val3535Ala)
c.10610T>C (p.Val3537Ala)
4g.186603922A>TCA358976989FAT1c.10604T>A (p.Val3535Glu)
c.10610T>A (p.Val3537Glu)
4g.186603923C>ACA358976990FAT1c.10603G>T (p.Val3535Leu)
c.10609G>T (p.Val3537Leu)
dbSNP
4g.186603923C=CA1520094270FAT1c.10603G= (p.Val3535=)
c.10609G= (p.Val3537=)
4g.186603923C>GCA358976991FAT1c.10603G>C (p.Val3535Leu)
c.10609G>C (p.Val3537Leu)
dbSNP
4g.186603923C>TCA3165308FAT1c.10603G>A (p.Val3535Ile)
c.10609G>A (p.Val3537Ile)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.186603924C>ACA358976992FAT1c.10602G>T (p.Arg3534Ser)
c.10608G>T (p.Arg3536Ser)
dbSNP
4g.186603924C>GCA358976993FAT1c.10602G>C (p.Arg3534Ser)
c.10608G>C (p.Arg3536Ser)
dbSNP
4g.186603924C>TCA442888119FAT1c.10602G>A (p.Arg3534=)
c.10608G>A (p.Arg3536=)
dbSNP
4g.186603925C>ACA358976994FAT1c.10601G>T (p.Arg3534Met)
c.10607G>T (p.Arg3536Met)
4g.186603925C=CA1520094271FAT1c.10601G= (p.Arg3534=)
c.10607G= (p.Arg3536=)
4g.186603925C>GCA358976995FAT1c.10601G>C (p.Arg3534Thr)
c.10607G>C (p.Arg3536Thr)
4g.186603925C>TCA112157443FAT1c.10601G>A (p.Arg3534Lys)
c.10607G>A (p.Arg3536Lys)
dbSNP
4g.186603926T>ACA358976996FAT1c.10600A>T (p.Arg3534Trp)
c.10606A>T (p.Arg3536Trp)
4g.186603926T>CCA358976997FAT1c.10600A>G (p.Arg3534Gly)
c.10606A>G (p.Arg3536Gly)
dbSNP
4g.186603926T>GCA442888132FAT1c.10600A>C (p.Arg3534=)
c.10606A>C (p.Arg3536=)
4g.186603927A=CA1520094272FAT1c.10599T= (p.Ile3533=)
c.10605T= (p.Ile3535=)
4g.186603927A>CCA358976998FAT1c.10599T>G (p.Ile3533Met)
c.10605T>G (p.Ile3535Met)
4g.186603927A>GCA3165309FAT1c.10599T>C (p.Ile3533=)
c.10605T>C (p.Ile3535=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.186603927A>TCA442888137FAT1c.10599T>A (p.Ile3533=)
c.10605T>A (p.Ile3535=)
4g.186603928A>CCA358976999FAT1c.10598T>G (p.Ile3533Ser)
c.10604T>G (p.Ile3535Ser)
4g.186603928A>GCA358977000FAT1c.10598T>C (p.Ile3533Thr)
c.10604T>C (p.Ile3535Thr)
gnomAD v4
4g.186603928A>TCA358977001FAT1c.10598T>A (p.Ile3533Asn)
c.10604T>A (p.Ile3535Asn)
dbSNP gnomAD v4
4g.186603929T>ACA358977002FAT1c.10597A>T (p.Ile3533Phe)
c.10603A>T (p.Ile3535Phe)
dbSNP
4g.186603929T>CCA3165310FAT1c.10597A>G (p.Ile3533Val)
c.10603A>G (p.Ile3535Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.186603929T>GCA358977003FAT1c.10597A>C (p.Ile3533Leu)
c.10603A>C (p.Ile3535Leu)
gnomAD v4
4g.186603929T=CA1520094273FAT1c.10597A= (p.Ile3533=)
c.10603A= (p.Ile3535=)
4g.186603930G>ACA442888160FAT1c.10596C>T (p.Asp3532=)
c.10602C>T (p.Asp3534=)
dbSNP gnomAD v4
4g.186603930G>CCA358977004FAT1c.10596C>G (p.Asp3532Glu)
c.10602C>G (p.Asp3534Glu)
dbSNP
4g.186603930G>TCA358977005FAT1c.10596C>A (p.Asp3532Glu)
c.10602C>A (p.Asp3534Glu)
4g.186603931T>ACA358977006FAT1c.10595A>T (p.Asp3532Val)
c.10601A>T (p.Asp3534Val)
dbSNP
4g.186603931T>CCA358977007FAT1c.10595A>G (p.Asp3532Gly)
c.10601A>G (p.Asp3534Gly)
gnomAD v4
4g.186603931T>GCA358977008FAT1c.10595A>C (p.Asp3532Ala)
c.10601A>C (p.Asp3534Ala)
4g.186603932C>ACA358977011FAT1c.10594G>T (p.Asp3532Tyr)
c.10600G>T (p.Asp3534Tyr)
dbSNP
4g.186603932C>GCA358977010FAT1c.10594G>C (p.Asp3532His)
c.10600G>C (p.Asp3534His)
dbSNP
4g.186603932C>TCA358977009FAT1c.10594G>A (p.Asp3532Asn)
c.10600G>A (p.Asp3534Asn)
dbSNP
4g.186603933A>CCA358977012FAT1c.10593T>G (p.Ile3531Met)
c.10599T>G (p.Ile3533Met)
4g.186603933A>GCA442888166FAT1c.10593T>C (p.Ile3531=)
c.10599T>C (p.Ile3533=)
dbSNP gnomAD v4
4g.186603933A>TCA442888167FAT1c.10593T>A (p.Ile3531=)
c.10599T>A (p.Ile3533=)
4g.186603934A>CCA358977013FAT1c.10592T>G (p.Ile3531Ser)
c.10598T>G (p.Ile3533Ser)
4g.186603934A>GCA358977014FAT1c.10592T>C (p.Ile3531Thr)
c.10598T>C (p.Ile3533Thr)
4g.186603934A>TCA358977015FAT1c.10592T>A (p.Ile3531Asn)
c.10598T>A (p.Ile3533Asn)
4g.186603935T>ACA358977016FAT1c.10591A>T (p.Ile3531Phe)
c.10597A>T (p.Ile3533Phe)
dbSNP gnomAD v2 gnomAD v4
4g.186603935T>CCA3165311FAT1c.10591A>G (p.Ile3531Val)
c.10597A>G (p.Ile3533Val)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.186603935T>GCA358977017FAT1c.10591A>C (p.Ile3531Leu)
c.10597A>C (p.Ile3533Leu)
4g.186603935T=CA1520094274FAT1c.10591A= (p.Ile3531=)
c.10597A= (p.Ile3533=)
4g.186603936G>ACA3165312FAT1c.10590C>T (p.Tyr3530=)
c.10596C>T (p.Tyr3532=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.186603936G>CCA358977018FAT1c.10590C>G (p.Tyr3530Ter)
c.10596C>G (p.Tyr3532Ter)
ClinVar dbSNP
4g.186603936G=CA1520094275FAT1c.10590C= (p.Tyr3530=)
c.10596C= (p.Tyr3532=)
4g.186603936G>TCA358977019FAT1c.10590C>A (p.Tyr3530Ter)
c.10596C>A (p.Tyr3532Ter)
4g.186603937T>ACA358977020FAT1c.10589A>T (p.Tyr3530Phe)
c.10595A>T (p.Tyr3532Phe)
dbSNP
4g.186603937T>CCA358977021FAT1c.10589A>G (p.Tyr3530Cys)
c.10595A>G (p.Tyr3532Cys)
dbSNP
4g.186603937T>GCA358977022FAT1c.10589A>C (p.Tyr3530Ser)
c.10595A>C (p.Tyr3532Ser)
4g.186603937dupCA917387971FAT1c.10589dup (p.Tyr3530Ter)
c.10595dup (p.Tyr3532Ter)
dbSNP
4g.186603938A>CCA358977025FAT1c.10588T>G (p.Tyr3530Asp)
c.10594T>G (p.Tyr3532Asp)
4g.186603938A>GCA358977023FAT1c.10588T>C (p.Tyr3530His)
c.10594T>C (p.Tyr3532His)
dbSNP
4g.186603938A>TCA358977024FAT1c.10588T>A (p.Tyr3530Asn)
c.10594T>A (p.Tyr3532Asn)
dbSNP
4g.186603939T>ACA442888185FAT1c.10587A>T (p.Thr3529=)
c.10593A>T (p.Thr3531=)
dbSNP
4g.186603939T>CCA3165313FAT1c.10587A>G (p.Thr3529=)
c.10593A>G (p.Thr3531=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.186603939T>GCA442888184FAT1c.10587A>C (p.Thr3529=)
c.10593A>C (p.Thr3531=)
4g.186603939T=CA1520094276FAT1c.10587A= (p.Thr3529=)
c.10593A= (p.Thr3531=)
4g.186603940G>ACA358977026FAT1c.10586C>T (p.Thr3529Ile)
c.10592C>T (p.Thr3531Ile)
dbSNP gnomAD v2 gnomAD v4
4g.186603940G>CCA358977027FAT1c.10586C>G (p.Thr3529Arg)
c.10592C>G (p.Thr3531Arg)
dbSNP
4g.186603940G=CA1520094277FAT1c.10586C= (p.Thr3529=)
c.10592C= (p.Thr3531=)
4g.186603940G>TCA358977028FAT1c.10586C>A (p.Thr3529Lys)
c.10592C>A (p.Thr3531Lys)
4g.186603941T>ACA358977029FAT1c.10585A>T (p.Thr3529Ser)
c.10591A>T (p.Thr3531Ser)
dbSNP
4g.186603941T>CCA3165314FAT1c.10585A>G (p.Thr3529Ala)
c.10591A>G (p.Thr3531Ala)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.186603941T>GCA358977030FAT1c.10585A>C (p.Thr3529Pro)
c.10591A>C (p.Thr3531Pro)
dbSNP
4g.186603941T=CA1520094278FAT1c.10585A= (p.Thr3529=)
c.10591A= (p.Thr3531=)
4g.186603942C>ACA358977031FAT1c.10584G>T (p.Leu3528Phe)
c.10590G>T (p.Leu3530Phe)
dbSNP gnomAD v4
4g.186603942C=CA1520094279FAT1c.10584G= (p.Leu3528=)
c.10590G= (p.Leu3530=)
4g.186603942C>GCA358977032FAT1c.10584G>C (p.Leu3528Phe)
c.10590G>C (p.Leu3530Phe)
dbSNP
4g.186603942C>TCA442888195FAT1c.10584G>A (p.Leu3528=)
c.10590G>A (p.Leu3530=)
dbSNP gnomAD v2 gnomAD v4
4g.186603943A>CCA358977033FAT1c.10583T>G (p.Leu3528Trp)
c.10589T>G (p.Leu3530Trp)
4g.186603943A>GCA358977034FAT1c.10583T>C (p.Leu3528Ser)
c.10589T>C (p.Leu3530Ser)
dbSNP
4g.186603943A>TCA358977035FAT1c.10583T>A (p.Leu3528Ter)
c.10589T>A (p.Leu3530Ter)
4g.186603944A>CCA358977037FAT1c.10582T>G (p.Leu3528Val)
c.10588T>G (p.Leu3530Val)
4g.186603944A>GCA442888207FAT1c.10582T>C (p.Leu3528=)
c.10588T>C (p.Leu3530=)
dbSNP
4g.186603944A>TCA358977036FAT1c.10582T>A (p.Leu3528Met)
c.10588T>A (p.Leu3530Met)
4g.186603945A=CA1520094280FAT1c.10581T= (p.Ser3527=)
c.10587T= (p.Ser3529=)
4g.186603945A>CCA442888212FAT1c.10581T>G (p.Ser3527=)
c.10587T>G (p.Ser3529=)
4g.186603945A>GCA3165315FAT1c.10581T>C (p.Ser3527=)
c.10587T>C (p.Ser3529=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.186603945A>TCA442888214FAT1c.10581T>A (p.Ser3527=)
c.10587T>A (p.Ser3529=)
dbSNP
4g.186603946G>ACA358977038FAT1c.10580C>T (p.Ser3527Phe)
c.10586C>T (p.Ser3529Phe)
dbSNP
4g.186603946G>CCA358977039FAT1c.10580C>G (p.Ser3527Cys)
c.10586C>G (p.Ser3529Cys)
dbSNP
4g.186603946G>TCA358977040FAT1c.10580C>A (p.Ser3527Tyr)
c.10586C>A (p.Ser3529Tyr)
4g.186603947A=CA1520094281FAT1c.10579T= (p.Ser3527=)
c.10585T= (p.Ser3529=)
4g.186603947A>CCA3165316FAT1c.10579T>G (p.Ser3527Ala)
c.10585T>G (p.Ser3529Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.186603947A>GCA358977041FAT1c.10579T>C (p.Ser3527Pro)
c.10585T>C (p.Ser3529Pro)
dbSNP
4g.186603947A>TCA358977042FAT1c.10579T>A (p.Ser3527Thr)
c.10585T>A (p.Ser3529Thr)
dbSNP
4g.186603948T>ACA442888228FAT1c.10578A>T (p.Ser3526=)
c.10584A>T (p.Ser3528=)
dbSNP
4g.186603948T>CCA442888233FAT1c.10578A>G (p.Ser3526=)
c.10584A>G (p.Ser3528=)
4g.186603948T>GCA442888235FAT1c.10578A>C (p.Ser3526=)
c.10584A>C (p.Ser3528=)
4g.186603949G>ACA358977045FAT1c.10577C>T (p.Ser3526Leu)
c.10583C>T (p.Ser3528Leu)
dbSNP
4g.186603949G>CCA358977043FAT1c.10577C>G (p.Ser3526Ter)
c.10583C>G (p.Ser3528Ter)
dbSNP
4g.186603949G>TCA358977044FAT1c.10577C>A (p.Ser3526Ter)
c.10583C>A (p.Ser3528Ter)
gnomAD v4
4g.186603949_186603950insGGAAGTTCCA2523064121FAT1c.10576_10577insGAACTTCC (p.Ser3526Ter)
c.10582_10583insGAACTTCC (p.Ser3528Ter)
4g.186603950A=CA1520094282FAT1c.10576T= (p.Ser3526=)
c.10582T= (p.Ser3528=)
4g.186603950A>CCA358977046FAT1c.10576T>G (p.Ser3526Ala)
c.10582T>G (p.Ser3528Ala)
dbSNP
4g.186603950A>GCA358977047FAT1c.10576T>C (p.Ser3526Pro)
c.10582T>C (p.Ser3528Pro)
ClinVar dbSNP COSMIC COSMIC
4g.186603950A>TCA358977048FAT1c.10576T>A (p.Ser3526Thr)
c.10582T>A (p.Ser3528Thr)
dbSNP
4g.186603951C>ACA358977049FAT1c.10575G>T (p.Leu3525Phe)
c.10581G>T (p.Leu3527Phe)
dbSNP gnomAD v4
4g.186603951C>GCA358977050FAT1c.10575G>C (p.Leu3525Phe)
c.10581G>C (p.Leu3527Phe)
dbSNP
4g.186603951C>TCA442888244FAT1c.10575G>A (p.Leu3525=)
c.10581G>A (p.Leu3527=)
dbSNP
4g.186603952A>CCA358977053FAT1c.10574T>G (p.Leu3525Trp)
c.10580T>G (p.Leu3527Trp)
4g.186603952A>GCA358977051FAT1c.10574T>C (p.Leu3525Ser)
c.10580T>C (p.Leu3527Ser)
dbSNP
4g.186603952A>TCA358977052FAT1c.10574T>A (p.Leu3525Ter)
c.10580T>A (p.Leu3527Ter)
dbSNP
4g.186603953A>CCA358977054FAT1c.10573T>G (p.Leu3525Val)
c.10579T>G (p.Leu3527Val)
dbSNP
4g.186603953A>GCA442888253FAT1c.10573T>C (p.Leu3525=)
c.10579T>C (p.Leu3527=)
4g.186603953A>TCA358977055FAT1c.10573T>A (p.Leu3525Met)
c.10579T>A (p.Leu3527Met)
dbSNP
4g.186603954C>ACA358977056FAT1c.10572G>T (p.Gln3524His)
c.10578G>T (p.Gln3526His)
4g.186603954C=CA1520094283FAT1c.10572G= (p.Gln3524=)
c.10578G= (p.Gln3526=)
4g.186603954C>GCA3165317FAT1c.10572G>C (p.Gln3524His)
c.10578G>C (p.Gln3526His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.186603954C>TCA442888259FAT1c.10572G>A (p.Gln3524=)
c.10578G>A (p.Gln3526=)
dbSNP
4g.186603955T>ACA358977057FAT1c.10571A>T (p.Gln3524Leu)
c.10577A>T (p.Gln3526Leu)
dbSNP
4g.186603955T>CCA358977058FAT1c.10571A>G (p.Gln3524Arg)
c.10577A>G (p.Gln3526Arg)
dbSNP
4g.186603955T>GCA358977059FAT1c.10571A>C (p.Gln3524Pro)
c.10577A>C (p.Gln3526Pro)
4g.186603956G>ACA358977060FAT1c.10570C>T (p.Gln3524Ter)
c.10576C>T (p.Gln3526Ter)
dbSNP COSMIC COSMIC
4g.186603956G>CCA358977061FAT1c.10570C>G (p.Gln3524Glu)
c.10576C>G (p.Gln3526Glu)
dbSNP
4g.186603956G>TCA358977062FAT1c.10570C>A (p.Gln3524Lys)
c.10576C>A (p.Gln3526Lys)
4g.186603957A>CCA442888265FAT1c.10569T>G (p.Pro3523=)
c.10575T>G (p.Pro3525=)
dbSNP
4g.186603957A>GCA442888266FAT1c.10569T>C (p.Pro3523=)
c.10575T>C (p.Pro3525=)
dbSNP
4g.186603957A>TCA442888269FAT1c.10569T>A (p.Pro3523=)
c.10575T>A (p.Pro3525=)
dbSNP
4g.186603958G>ACA358977063FAT1c.10568C>T (p.Pro3523Leu)
c.10574C>T (p.Pro3525Leu)
dbSNP
4g.186603958G>CCA358977064FAT1c.10568C>G (p.Pro3523Arg)
c.10574C>G (p.Pro3525Arg)
dbSNP
4g.186603958G>TCA358977065FAT1c.10568C>A (p.Pro3523His)
c.10574C>A (p.Pro3525His)
dbSNP
4g.186603959G>ACA358977066FAT1c.10567C>T (p.Pro3523Ser)
c.10573C>T (p.Pro3525Ser)
dbSNP gnomAD v2 gnomAD v4
4g.186603959G>CCA358977068FAT1c.10567C>G (p.Pro3523Ala)
c.10573C>G (p.Pro3525Ala)
dbSNP
4g.186603959G=CA1520094284FAT1c.10567C= (p.Pro3523=)
c.10573C= (p.Pro3525=)
4g.186603959G>TCA358977067FAT1c.10567C>A (p.Pro3523Thr)
c.10573C>A (p.Pro3525Thr)
4g.186603960C>ACA358977069FAT1c.10566G>T (p.Lys3522Asn)
c.10572G>T (p.Lys3524Asn)
dbSNP
4g.186603960C=CA1520094285FAT1c.10566G= (p.Lys3522=)
c.10572G= (p.Lys3524=)
4g.186603960C>GCA358977070FAT1c.10566G>C (p.Lys3522Asn)
c.10572G>C (p.Lys3524Asn)
dbSNP
4g.186603960C>TCA442888282FAT1c.10566G>A (p.Lys3522=)
c.10572G>A (p.Lys3524=)
dbSNP gnomAD v3 gnomAD v4
4g.186603961T>ACA358977071FAT1c.10565A>T (p.Lys3522Met)
c.10571A>T (p.Lys3524Met)
dbSNP
4g.186603961T>CCA358977072FAT1c.10565A>G (p.Lys3522Arg)
c.10571A>G (p.Lys3524Arg)
dbSNP
4g.186603961T>GCA358977073FAT1c.10565A>C (p.Lys3522Thr)
c.10571A>C (p.Lys3524Thr)
4g.186603962T>ACA358977074FAT1c.10564A>T (p.Lys3522Ter)
c.10570A>T (p.Lys3524Ter)
4g.186603962T>CCA358977075FAT1c.10564A>G (p.Lys3522Glu)
c.10570A>G (p.Lys3524Glu)
dbSNP gnomAD v2 gnomAD v4
4g.186603962T>GCA358977076FAT1c.10564A>C (p.Lys3522Gln)
c.10570A>C (p.Lys3524Gln)
4g.186603962T=CA1520094286FAT1c.10564A= (p.Lys3522=)
c.10570A= (p.Lys3524=)
4g.186603963T>ACA442888296FAT1c.10563A>T (p.Gly3521=)
c.10569A>T (p.Gly3523=)
4g.186603963T>CCA442888298FAT1c.10563A>G (p.Gly3521=)
c.10569A>G (p.Gly3523=)
4g.186603963T>GCA442888300FAT1c.10563A>C (p.Gly3521=)
c.10569A>C (p.Gly3523=)
4g.186603964C>ACA358977077FAT1c.10562G>T (p.Gly3521Val)
c.10568G>T (p.Gly3523Val)
dbSNP
4g.186603964C>GCA358977078FAT1c.10562G>C (p.Gly3521Ala)
c.10568G>C (p.Gly3523Ala)
dbSNP
4g.186603964C>TCA358977079FAT1c.10562G>A (p.Gly3521Glu)
c.10568G>A (p.Gly3523Glu)
dbSNP
4g.186603965C>ACA358977080FAT1c.10561G>T (p.Gly3521Ter)
c.10567G>T (p.Gly3523Ter)
dbSNP COSMIC COSMIC
4g.186603965C>GCA358977081FAT1c.10561G>C (p.Gly3521Arg)
c.10567G>C (p.Gly3523Arg)
dbSNP
4g.186603965C>TCA358977082FAT1c.10561G>A (p.Gly3521Arg)
c.10567G>A (p.Gly3523Arg)
dbSNP
4g.186603966A>CCA358977083FAT1c.10560T>G (p.Asn3520Lys)
c.10566T>G (p.Asn3522Lys)
4g.186603966A>GCA442888308FAT1c.10560T>C (p.Asn3520=)
c.10566T>C (p.Asn3522=)
4g.186603966A>TCA358977084FAT1c.10560T>A (p.Asn3520Lys)
c.10566T>A (p.Asn3522Lys)
4g.186603967T>ACA358977085FAT1c.10559A>T (p.Asn3520Ile)
c.10565A>T (p.Asn3522Ile)
dbSNP
4g.186603967T>CCA358977086FAT1c.10559A>G (p.Asn3520Ser)
c.10565A>G (p.Asn3522Ser)
4g.186603967T>GCA358977087FAT1c.10559A>C (p.Asn3520Thr)
c.10565A>C (p.Asn3522Thr)
dbSNP gnomAD v3 gnomAD v4
4g.186603967T=CA1520094287FAT1c.10559A= (p.Asn3520=)
c.10565A= (p.Asn3522=)
4g.186603968T>ACA358977088FAT1c.10558A>T (p.Asn3520Tyr)
c.10564A>T (p.Asn3522Tyr)
dbSNP
4g.186603968T>CCA358977089FAT1c.10558A>G (p.Asn3520Asp)
c.10564A>G (p.Asn3522Asp)
4g.186603968T>GCA3165318FAT1c.10558A>C (p.Asn3520His)
c.10564A>C (p.Asn3522His)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.186603968T=CA1520094288FAT1c.10558A= (p.Asn3520=)
c.10564A= (p.Asn3522=)
4g.186603969A=CA1520094289FAT1c.10557T= (p.Asp3519=)
c.10563T= (p.Asp3521=)
4g.186603969A>CCA358977090FAT1c.10557T>G (p.Asp3519Glu)
c.10563T>G (p.Asp3521Glu)
dbSNP
4g.186603969A>GCA3165319FAT1c.10557T>C (p.Asp3519=)
c.10563T>C (p.Asp3521=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.186603969A>TCA358977091FAT1c.10557T>A (p.Asp3519Glu)
c.10563T>A (p.Asp3521Glu)
dbSNP
4g.186603970T>ACA358977092FAT1c.10556A>T (p.Asp3519Val)
c.10562A>T (p.Asp3521Val)
dbSNP
4g.186603970T>CCA358977093FAT1c.10556A>G (p.Asp3519Gly)
c.10562A>G (p.Asp3521Gly)
gnomAD v4
4g.186603970T>GCA358977094FAT1c.10556A>C (p.Asp3519Ala)
c.10562A>C (p.Asp3521Ala)
4g.186603971C>ACA358977095FAT1c.10555G>T (p.Asp3519Tyr)
c.10561G>T (p.Asp3521Tyr)
dbSNP
4g.186603971C=CA1520094290FAT1c.10555G= (p.Asp3519=)
c.10561G= (p.Asp3521=)
4g.186603971C>GCA358977097FAT1c.10555G>C (p.Asp3519His)
c.10561G>C (p.Asp3521His)
dbSNP
4g.186603971C>TCA358977096FAT1c.10555G>A (p.Asp3519Asn)
c.10561G>A (p.Asp3521Asn)
dbSNP
4g.186603972T>ACA442888327FAT1c.10554A>T (p.Ala3518=)
c.10560A>T (p.Ala3520=)
dbSNP
4g.186603972T>CCA442888329FAT1c.10554A>G (p.Ala3518=)
c.10560A>G (p.Ala3520=)
gnomAD v4
4g.186603972T>GCA442888330FAT1c.10554A>C (p.Ala3518=)
c.10560A>C (p.Ala3520=)
4g.186603973G>ACA358977098FAT1c.10553C>T (p.Ala3518Val)
c.10559C>T (p.Ala3520Val)
gnomAD v4
4g.186603973G>CCA358977101FAT1c.10553C>G (p.Ala3518Gly)
c.10559C>G (p.Ala3520Gly)
4g.186603973G>TCA358977100FAT1c.10553C>A (p.Ala3518Glu)
c.10559C>A (p.Ala3520Glu)

Number of alleles fetched