Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.48750791A=CA2340052952FUT1c.491T= (p.Leu164=)
c.860T= (p.Leu287=)
19g.48750791A>CCA406703001FUT1c.491T>G (p.Leu164Arg)
c.860T>G (p.Leu287Arg)
19g.48750791A>GCA406703002FUT1c.491T>C (p.Leu164Pro)
c.860T>C (p.Leu287Pro)
19g.48750791A>TCA251323FUT1c.491T>A (p.Leu164His)
c.860T>A (p.Leu287His)
ClinVar dbSNP
19g.48750792G>ACA406703005FUT1c.490C>T (p.Leu164Phe)
c.859C>T (p.Leu287Phe)
19g.48750792G>CCA406703003FUT1c.490C>G (p.Leu164Val)
c.859C>G (p.Leu287Val)
19g.48750792G>TCA406703004FUT1c.490C>A (p.Leu164Ile)
c.859C>A (p.Leu287Ile)
19g.48750793C>ACA406703006FUT1c.489G>T (p.Lys163Asn)
c.858G>T (p.Lys286Asn)
19g.48750793C=CA2340052955FUT1c.489G= (p.Lys163=)
c.858G= (p.Lys286=)
19g.48750793C>GCA406703007FUT1c.489G>C (p.Lys163Asn)
c.858G>C (p.Lys286Asn)
19g.48750793C>TCA508274628FUT1c.489G>A (p.Lys163=)
c.858G>A (p.Lys286=)
dbSNP
19g.48750794T>ACA406703008FUT1c.488A>T (p.Lys163Met)
c.857A>T (p.Lys286Met)
19g.48750794T>CCA406703009FUT1c.488A>G (p.Lys163Arg)
c.857A>G (p.Lys286Arg)
gnomAD v4
19g.48750794T>GCA406703010FUT1c.488A>C (p.Lys163Thr)
c.857A>C (p.Lys286Thr)
19g.48750795T>ACA406703011FUT1c.487A>T (p.Lys163Ter)
c.856A>T (p.Lys286Ter)
19g.48750795T>CCA406703012FUT1c.487A>G (p.Lys163Glu)
c.856A>G (p.Lys286Glu)
19g.48750795T>GCA406703013FUT1c.487A>C (p.Lys163Gln)
c.856A>C (p.Lys286Gln)
19g.48750796C>ACA508274632FUT1c.486G>T (p.Leu162=)
c.855G>T (p.Leu285=)
19g.48750796C>GCA508274633FUT1c.486G>C (p.Leu162=)
c.855G>C (p.Leu285=)
19g.48750796C>TCA508274634FUT1c.486G>A (p.Leu162=)
c.855G>A (p.Leu285=)
19g.48750797A>CCA406703014FUT1c.485T>G (p.Leu162Arg)
c.854T>G (p.Leu285Arg)
19g.48750797A>GCA406703015FUT1c.485T>C (p.Leu162Pro)
c.854T>C (p.Leu285Pro)
19g.48750797A>TCA406703016FUT1c.485T>A (p.Leu162Gln)
c.854T>A (p.Leu285Gln)
19g.48750798G>ACA508274637FUT1c.484C>T (p.Leu162=)
c.853C>T (p.Leu285=)
19g.48750798G>CCA406703018FUT1c.484C>G (p.Leu162Val)
c.853C>G (p.Leu285Val)
19g.48750798G>TCA406703017FUT1c.484C>A (p.Leu162Met)
c.853C>A (p.Leu285Met)
19g.48750799G>ACA508274639FUT1c.483C>T (p.Phe161=)
c.852C>T (p.Phe284=)
gnomAD v4 COSMIC
19g.48750799G>CCA406703019FUT1c.483C>G (p.Phe161Leu)
c.852C>G (p.Phe284Leu)
gnomAD v4
19g.48750799G>TCA406703020FUT1c.483C>A (p.Phe161Leu)
c.852C>A (p.Phe284Leu)
gnomAD v4
19g.48750800A>CCA406703021FUT1c.482T>G (p.Phe161Cys)
c.851T>G (p.Phe284Cys)
19g.48750800A>GCA406703022FUT1c.482T>C (p.Phe161Ser)
c.851T>C (p.Phe284Ser)
19g.48750800A>TCA406703023FUT1c.482T>A (p.Phe161Tyr)
c.851T>A (p.Phe284Tyr)
19g.48750801A=CA2340052956FUT1c.481T= (p.Phe161=)
c.850T= (p.Phe284=)
19g.48750801A>CCA406703024FUT1c.481T>G (p.Phe161Val)
c.850T>G (p.Phe284Val)
dbSNP
19g.48750801A>GCA406703025FUT1c.481T>C (p.Phe161Leu)
c.850T>C (p.Phe284Leu)
19g.48750801A>TCA406703026FUT1c.481T>A (p.Phe161Ile)
c.850T>A (p.Phe284Ile)
19g.48750802A>CCA508274641FUT1c.480T>G (p.Pro160=)
c.849T>G (p.Pro283=)
19g.48750802A>GCA508274642FUT1c.480T>C (p.Pro160=)
c.849T>C (p.Pro283=)
gnomAD v4
19g.48750802A>TCA508274644FUT1c.480T>A (p.Pro160=)
c.849T>A (p.Pro283=)
19g.48750803G>ACA406703027FUT1c.479C>T (p.Pro160Leu)
c.848C>T (p.Pro283Leu)
dbSNP gnomAD v3 gnomAD v4
19g.48750803G>CCA406703028FUT1c.479C>G (p.Pro160Arg)
c.848C>G (p.Pro283Arg)
19g.48750803G=CA2340052958FUT1c.479C= (p.Pro160=)
c.848C= (p.Pro283=)
19g.48750803G>TCA406703029FUT1c.479C>A (p.Pro160His)
c.848C>A (p.Pro283His)
19g.48750804G>ACA406703030FUT1c.478C>T (p.Pro160Ser)
c.847C>T (p.Pro283Ser)
19g.48750804G>CCA406703031FUT1c.478C>G (p.Pro160Ala)
c.847C>G (p.Pro283Ala)
19g.48750804G>TCA406703032FUT1c.478C>A (p.Pro160Thr)
c.847C>A (p.Pro283Thr)
19g.48750805A=CA2340052960FUT1c.477T= (p.Asp159=)
c.846T= (p.Asp282=)
19g.48750805A>CCA406703034FUT1c.477T>G (p.Asp159Glu)
c.846T>G (p.Asp282Glu)
19g.48750805A>GCA9557731FUT1c.477T>C (p.Asp159=)
c.846T>C (p.Asp282=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.48750805A>TCA406703033FUT1c.477T>A (p.Asp159Glu)
c.846T>A (p.Asp282Glu)
dbSNP
19g.48750806T>ACA406703035FUT1c.476A>T (p.Asp159Val)
c.845A>T (p.Asp282Val)
COSMIC
19g.48750806T>CCA406703036FUT1c.476A>G (p.Asp159Gly)
c.845A>G (p.Asp282Gly)
gnomAD v4
19g.48750806T>GCA406703037FUT1c.476A>C (p.Asp159Ala)
c.845A>C (p.Asp282Ala)
19g.48750807C>ACA406703038FUT1c.475G>T (p.Asp159Tyr)
c.844G>T (p.Asp282Tyr)
19g.48750807C>GCA406703039FUT1c.475G>C (p.Asp159His)
c.844G>C (p.Asp282His)
19g.48750807C>TCA406703040FUT1c.475G>A (p.Asp159Asn)
c.844G>A (p.Asp282Asn)
19g.48750808T>ACA406703041FUT1c.474A>T (p.Arg158Ser)
c.843A>T (p.Arg281Ser)
19g.48750808T>CCA508274648FUT1c.474A>G (p.Arg158=)
c.843A>G (p.Arg281=)
19g.48750808T>GCA406703042FUT1c.474A>C (p.Arg158Ser)
c.843A>C (p.Arg281Ser)
19g.48750809C>ACA406703043FUT1c.473G>T (p.Arg158Ile)
c.842G>T (p.Arg281Ile)
19g.48750809C=CA2340052962FUT1c.473G= (p.Arg158=)
c.842G= (p.Arg281=)
19g.48750809C>GCA406703044FUT1c.473G>C (p.Arg158Thr)
c.842G>C (p.Arg281Thr)
19g.48750809C>TCA9557732FUT1c.473G>A (p.Arg158Lys)
c.842G>A (p.Arg281Lys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.48750810T>ACA406703045FUT1c.472A>T (p.Arg158Ter)
c.841A>T (p.Arg281Ter)
19g.48750810T>CCA406703046FUT1c.472A>G (p.Arg158Gly)
c.841A>G (p.Arg281Gly)
dbSNP gnomAD v2 gnomAD v4
19g.48750810T>GCA508274651FUT1c.472A>C (p.Arg158=)
c.841A>C (p.Arg281=)
19g.48750810T=CA2340052964FUT1c.472A= (p.Arg158=)
c.841A= (p.Arg281=)
19g.48750811C>ACA406703047FUT1c.471G>T (p.Leu157Phe)
c.840G>T (p.Leu280Phe)
dbSNP gnomAD v2 gnomAD v4
19g.48750811C=CA2340052966FUT1c.471G= (p.Leu157=)
c.840G= (p.Leu280=)
19g.48750811C>GCA406703048FUT1c.471G>C (p.Leu157Phe)
c.840G>C (p.Leu280Phe)
gnomAD v4 COSMIC
19g.48750811C>TCA508274652FUT1c.471G>A (p.Leu157=)
c.840G>A (p.Leu280=)
dbSNP gnomAD v3 gnomAD v4
19g.48750812A>CCA406703049FUT1c.470T>G (p.Leu157Trp)
c.839T>G (p.Leu280Trp)
19g.48750812A>GCA406703051FUT1c.470T>C (p.Leu157Ser)
c.839T>C (p.Leu280Ser)
19g.48750812A>TCA406703050FUT1c.470T>A (p.Leu157Ter)
c.839T>A (p.Leu280Ter)
19g.48750813A>CCA406703052FUT1c.469T>G (p.Leu157Val)
c.838T>G (p.Leu280Val)
19g.48750813A>GCA508274656FUT1c.469T>C (p.Leu157=)
c.838T>C (p.Leu280=)
19g.48750813A>TCA406703053FUT1c.469T>A (p.Leu157Met)
c.838T>A (p.Leu280Met)
19g.48750814G>ACA508274657FUT1c.468C>T (p.Asp156=)
c.837C>T (p.Asp279=)
gnomAD v4
19g.48750814G>CCA9557733FUT1c.468C>G (p.Asp156Glu)
c.837C>G (p.Asp279Glu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.48750814G=CA2340052968FUT1c.468C= (p.Asp156=)
c.837C= (p.Asp279=)
19g.48750814G>TCA9557734FUT1c.468C>A (p.Asp156Glu)
c.837C>A (p.Asp279Glu)
dbSNP ExAC
19g.48750815T>ACA406703054FUT1c.467A>T (p.Asp156Val)
c.836A>T (p.Asp279Val)
19g.48750815T>CCA406703056FUT1c.467A>G (p.Asp156Gly)
c.836A>G (p.Asp279Gly)
gnomAD v4
19g.48750815T>GCA406703055FUT1c.467A>C (p.Asp156Ala)
c.836A>C (p.Asp279Ala)
19g.48750816C>ACA406703057FUT1c.466G>T (p.Asp156Tyr)
c.835G>T (p.Asp279Tyr)
19g.48750816C=CA2340052970FUT1c.466G= (p.Asp156=)
c.835G= (p.Asp279=)
19g.48750816C>GCA406703058FUT1c.466G>C (p.Asp156His)
c.835G>C (p.Asp279His)
19g.48750816C>TCA9557735FUT1c.466G>A (p.Asp156Asn)
c.835G>A (p.Asp279Asn)
dbSNP ExAC gnomAD v2
19g.48750817C>ACA508274660FUT1c.465G>T (p.Ala155=)
c.834G>T (p.Ala278=)
19g.48750817C=CA2340052972FUT1c.465G= (p.Ala155=)
c.834G= (p.Ala278=)
19g.48750817C>GCA508274662FUT1c.465G>C (p.Ala155=)
c.834G>C (p.Ala278=)
19g.48750817C>TCA508274661FUT1c.465G>A (p.Ala155=)
c.834G>A (p.Ala278=)
dbSNP gnomAD v2 gnomAD v4
19g.48750818G>ACA406703059FUT1c.464C>T (p.Ala155Val)
c.833C>T (p.Ala278Val)
gnomAD v4 COSMIC
19g.48750818G>CCA406703060FUT1c.464C>G (p.Ala155Gly)
c.833C>G (p.Ala278Gly)
19g.48750818G>TCA406703061FUT1c.464C>A (p.Ala155Glu)
c.833C>A (p.Ala278Glu)
19g.48750819C>ACA9557736FUT1c.463G>T (p.Ala155Ser)
c.832G>T (p.Ala278Ser)
dbSNP ExAC
19g.48750819C=CA2340052974FUT1c.463G= (p.Ala155=)
c.832G= (p.Ala278=)
19g.48750819C>GCA406703062FUT1c.463G>C (p.Ala155Pro)
c.832G>C (p.Ala278Pro)
19g.48750819C>TCA406703063FUT1c.463G>A (p.Ala155Thr)
c.832G>A (p.Ala278Thr)
19g.48750820G>ACA9557737FUT1c.462C>T (p.Tyr154=)
c.831C>T (p.Tyr277=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.48750820G>CCA406703064FUT1c.462C>G (p.Tyr154Ter)
c.831C>G (p.Tyr277Ter)
gnomAD v4
19g.48750820G=CA2340052976FUT1c.462C= (p.Tyr154=)
c.831C= (p.Tyr277=)
19g.48750820G>TCA406703065FUT1c.462C>A (p.Tyr154Ter)
c.831C>A (p.Tyr277Ter)
dbSNP
19g.48750821T>ACA406703068FUT1c.461A>T (p.Tyr154Phe)
c.830A>T (p.Tyr277Phe)
19g.48750821T>CCA406703066FUT1c.461A>G (p.Tyr154Cys)
c.830A>G (p.Tyr277Cys)
COSMIC
19g.48750821T>GCA406703067FUT1c.461A>C (p.Tyr154Ser)
c.830A>C (p.Tyr277Ser)
19g.48750822A=CA2340052979FUT1c.460T= (p.Tyr154=)
c.829T= (p.Tyr277=)
19g.48750822A>CCA406703069FUT1c.460T>G (p.Tyr154Asp)
c.829T>G (p.Tyr277Asp)
dbSNP
19g.48750822A>GCA9557738FUT1c.460T>C (p.Tyr154His)
c.829T>C (p.Tyr277His)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.48750822A>TCA406703070FUT1c.460T>A (p.Tyr154Asn)
c.829T>A (p.Tyr277Asn)
19g.48750822_48750825delinsACTCCA2340052981FUT1c.457_460delinsGAGT (p.Glu153=)
c.826_829delinsGAGT (p.Glu276=)
19g.48750823C>ACA406703071FUT1c.459G>T (p.Glu153Asp)
c.828G>T (p.Glu276Asp)
19g.48750823C>GCA406703072FUT1c.459G>C (p.Glu153Asp)
c.828G>C (p.Glu276Asp)
19g.48750823C>TCA508274669FUT1c.459G>A (p.Glu153=)
c.828G>A (p.Glu276=)
gnomAD v4
19g.48750827_48750829delCA633888604FUT1c.457_459del (p.Glu153del)
c.826_828del (p.Glu276del)
dbSNP gnomAD v2 gnomAD v4
19g.48750824T>ACA406703073FUT1c.458A>T (p.Glu153Val)
c.827A>T (p.Glu276Val)
dbSNP
19g.48750824T>CCA406703074FUT1c.458A>G (p.Glu153Gly)
c.827A>G (p.Glu276Gly)
19g.48750824T>GCA406703075FUT1c.458A>C (p.Glu153Ala)
c.827A>C (p.Glu276Ala)
19g.48750824T=CA2340052983FUT1c.458A= (p.Glu153=)
c.827A= (p.Glu276=)
19g.48750825C>ACA406703076FUT1c.457G>T (p.Glu153Ter)
c.826G>T (p.Glu276Ter)
19g.48750825C>GCA406703077FUT1c.457G>C (p.Glu153Gln)
c.826G>C (p.Glu276Gln)
19g.48750825C>TCA406703078FUT1c.457G>A (p.Glu153Lys)
c.826G>A (p.Glu276Lys)
19g.48750826C>ACA406703079FUT1c.456G>T (p.Glu152Asp)
c.825G>T (p.Glu275Asp)
19g.48750826C=CA2340052986FUT1c.456G= (p.Glu152=)
c.825G= (p.Glu275=)
19g.48750826C>GCA406703080FUT1c.456G>C (p.Glu152Asp)
c.825G>C (p.Glu275Asp)
19g.48750826C>TCA508274675FUT1c.456G>A (p.Glu152=)
c.825G>A (p.Glu275=)
dbSNP gnomAD v3 gnomAD v4
19g.48750826_48750833delinsCTCCGACACA2340052985FUT1c.449_456delinsTGTCGGAG (p.Met150=)
c.818_825delinsTGTCGGAG (p.Met273=)
19g.48750827T>ACA406703081FUT1c.455A>T (p.Glu152Val)
c.824A>T (p.Glu275Val)
19g.48750827T>CCA406703082FUT1c.455A>G (p.Glu152Gly)
c.824A>G (p.Glu275Gly)
19g.48750827T>GCA406703083FUT1c.455A>C (p.Glu152Ala)
c.824A>C (p.Glu275Ala)
gnomAD v4
19g.48750827_48750828delinsTCCA2340052988FUT1c.454_455delinsGA (p.Glu152=)
c.823_824delinsGA (p.Glu275=)
19g.48750830_48750836delCA996628921FUT1c.449_455del (p.Met150ArgfsTer6)
c.818_824del (p.Met273ArgfsTer6)
dbSNP gnomAD v3 gnomAD v4
19g.48750828C>ACA406703084FUT1c.454G>T (p.Glu152Ter)
c.823G>T (p.Glu275Ter)
gnomAD v4
19g.48750828C=CA2340052990FUT1c.454G= (p.Glu152=)
c.823G= (p.Glu275=)
19g.48750828C>GCA9557739FUT1c.454G>C (p.Glu152Gln)
c.823G>C (p.Glu275Gln)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.48750828C>TCA406703085FUT1c.454G>A (p.Glu152Lys)
c.823G>A (p.Glu275Lys)
dbSNP gnomAD v3 gnomAD v4
19g.48750829delCA406703086FUT1c.454del (p.Glu152ArgfsTer6)
c.823del (p.Glu275ArgfsTer6)
dbSNP gnomAD v3 gnomAD v4
19g.48750829C>ACA508274680FUT1c.453G>T (p.Ser151=)
c.822G>T (p.Ser274=)
dbSNP
19g.48750829C=CA2340052992FUT1c.453G= (p.Ser151=)
c.822G= (p.Ser274=)
19g.48750829C>GCA9557740FUT1c.453G>C (p.Ser151=)
c.822G>C (p.Ser274=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.48750829C>TCA508274681FUT1c.453G>A (p.Ser151=)
c.822G>A (p.Ser274=)
dbSNP gnomAD v3 gnomAD v4 COSMIC
19g.48750830G>ACA9557741FUT1c.452C>T (p.Ser151Leu)
c.821C>T (p.Ser274Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.48750830G>CCA406703087FUT1c.452C>G (p.Ser151Trp)
c.821C>G (p.Ser274Trp)
19g.48750830G=CA2340052995FUT1c.452C= (p.Ser151=)
c.821C= (p.Ser274=)
19g.48750830G>TCA406703088FUT1c.452C>A (p.Ser151Ter)
c.821C>A (p.Ser274Ter)
19g.48750831A>CCA406703091FUT1c.451T>G (p.Ser151Ala)
c.820T>G (p.Ser274Ala)
19g.48750831A>GCA406703090FUT1c.451T>C (p.Ser151Pro)
c.820T>C (p.Ser274Pro)
19g.48750831A>TCA406703089FUT1c.451T>A (p.Ser151Thr)
c.820T>A (p.Ser274Thr)
gnomAD v4
19g.48750832_48750837dupCA996628933FUT1c.446_451dup (p.Met150_Ser151insTrpMet)
c.815_820dup (p.Met273_Ser274insTrpMet)
dbSNP gnomAD v3 gnomAD v4
19g.48750832C>ACA406703092FUT1c.450G>T (p.Met150Ile)
c.819G>T (p.Met273Ile)
19g.48750832C>GCA406703093FUT1c.450G>C (p.Met150Ile)
c.819G>C (p.Met273Ile)
19g.48750832C>TCA406703094FUT1c.450G>A (p.Met150Ile)
c.819G>A (p.Met273Ile)
19g.48750833A>CCA406703095FUT1c.449T>G (p.Met150Arg)
c.818T>G (p.Met273Arg)
19g.48750833A>GCA406703096FUT1c.449T>C (p.Met150Thr)
c.818T>C (p.Met273Thr)
gnomAD v4
19g.48750833A>TCA406703097FUT1c.449T>A (p.Met150Lys)
c.818T>A (p.Met273Lys)
19g.48750834T>ACA406703098FUT1c.448A>T (p.Met150Leu)
c.817A>T (p.Met273Leu)
19g.48750834T>CCA406703099FUT1c.448A>G (p.Met150Val)
c.817A>G (p.Met273Val)
19g.48750834T>GCA406703100FUT1c.448A>C (p.Met150Leu)
c.817A>C (p.Met273Leu)
19g.48750835C>ACA9557742FUT1c.447G>T (p.Trp149Cys)
c.816G>T (p.Trp272Cys)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.48750835C=CA2340052998FUT1c.447G= (p.Trp149=)
c.816G= (p.Trp272=)
19g.48750835C>GCA406703101FUT1c.447G>C (p.Trp149Cys)
c.816G>C (p.Trp272Cys)
19g.48750835C>TCA406703102FUT1c.447G>A (p.Trp149Ter)
c.816G>A (p.Trp272Ter)
19g.48750836delCA2586255172FUT1c.447del (p.Trp149Ter)
c.816del (p.Trp272Ter)
gnomAD v4
19g.48750836C>ACA406703105FUT1c.446G>T (p.Trp149Leu)
c.815G>T (p.Trp272Leu)
19g.48750836C=CA2340052999FUT1c.446G= (p.Trp149=)
c.815G= (p.Trp272=)
19g.48750836C>GCA406703104FUT1c.446G>C (p.Trp149Ser)
c.815G>C (p.Trp272Ser)
dbSNP gnomAD v4
19g.48750836C>TCA406703103FUT1c.446G>A (p.Trp149Ter)
c.815G>A (p.Trp272Ter)
gnomAD v4
19g.48750837A>CCA406703106FUT1c.445T>G (p.Trp149Gly)
c.814T>G (p.Trp272Gly)
19g.48750837A>GCA406703108FUT1c.445T>C (p.Trp149Arg)
c.814T>C (p.Trp272Arg)
19g.48750837A>TCA406703107FUT1c.445T>A (p.Trp149Arg)
c.814T>A (p.Trp272Arg)
19g.48750838G>ACA508274695FUT1c.444C>T (p.Asp148=)
c.813C>T (p.Asp271=)
19g.48750838G>CCA406703109FUT1c.444C>G (p.Asp148Glu)
c.813C>G (p.Asp271Glu)
dbSNP gnomAD v4
19g.48750838G=CA2340053001FUT1c.444C= (p.Asp148=)
c.813C= (p.Asp271=)
19g.48750838G>TCA406703110FUT1c.444C>A (p.Asp148Glu)
c.813C>A (p.Asp271Glu)
19g.48750839T>ACA406703111FUT1c.443A>T (p.Asp148Val)
c.812A>T (p.Asp271Val)
19g.48750839T>CCA406703112FUT1c.443A>G (p.Asp148Gly)
c.812A>G (p.Asp271Gly)
19g.48750839T>GCA406703113FUT1c.443A>C (p.Asp148Ala)
c.812A>C (p.Asp271Ala)
19g.48750840C>ACA9557743FUT1c.442G>T (p.Asp148Tyr)
c.811G>T (p.Asp271Tyr)
dbSNP ExAC gnomAD v2
19g.48750840C=CA2340053003FUT1c.442G= (p.Asp148=)
c.811G= (p.Asp271=)
19g.48750840C>GCA406703114FUT1c.442G>C (p.Asp148His)
c.811G>C (p.Asp271His)
19g.48750840C>TCA406703115FUT1c.442G>A (p.Asp148Asn)
c.811G>A (p.Asp271Asn)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.48750841G>ACA9557744FUT1c.441C>T (p.His147=)
c.810C>T (p.His270=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.48750841G>CCA406703116FUT1c.441C>G (p.His147Gln)
c.810C>G (p.His270Gln)
dbSNP gnomAD v2 gnomAD v4
19g.48750841G=CA2340053006FUT1c.441C= (p.His147=)
c.810C= (p.His270=)
19g.48750841G>TCA406703117FUT1c.441C>A (p.His147Gln)
c.810C>A (p.His270Gln)
19g.48750842T>ACA9557745FUT1c.440A>T (p.His147Leu)
c.809A>T (p.His270Leu)
dbSNP ExAC gnomAD v2
19g.48750842T>CCA406703119FUT1c.440A>G (p.His147Arg)
c.809A>G (p.His270Arg)
19g.48750842T>GCA406703118FUT1c.440A>C (p.His147Pro)
c.809A>C (p.His270Pro)
19g.48750842T=CA2340053008FUT1c.440A= (p.His147=)
c.809A= (p.His270=)
19g.48750843G>ACA406703120FUT1c.439C>T (p.His147Tyr)
c.808C>T (p.His270Tyr)
19g.48750843G>CCA406703121FUT1c.439C>G (p.His147Asp)
c.808C>G (p.His270Asp)
19g.48750843G>TCA406703122FUT1c.439C>A (p.His147Asn)
c.808C>A (p.His270Asn)
19g.48750844A>CCA508274708FUT1c.438T>G (p.Leu146=)
c.807T>G (p.Leu269=)
19g.48750844A>GCA508274709FUT1c.438T>C (p.Leu146=)
c.807T>C (p.Leu269=)
19g.48750844A>TCA508274710FUT1c.438T>A (p.Leu146=)
c.807T>A (p.Leu269=)
19g.48750845A>CCA406703123FUT1c.437T>G (p.Leu146Arg)
c.806T>G (p.Leu269Arg)
19g.48750845A>GCA406703124FUT1c.437T>C (p.Leu146Pro)
c.806T>C (p.Leu269Pro)
19g.48750845A>TCA406703125FUT1c.437T>A (p.Leu146His)
c.806T>A (p.Leu269His)
19g.48750846G>ACA406703126FUT1c.436C>T (p.Leu146Phe)
c.805C>T (p.Leu269Phe)
dbSNP gnomAD v2 gnomAD v4
19g.48750846G>CCA9557746FUT1c.436C>G (p.Leu146Val)
c.805C>G (p.Leu269Val)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.48750846G=CA2340053018FUT1c.436C= (p.Leu146=)
c.805C= (p.Leu269=)
19g.48750846G>TCA406703127FUT1c.436C>A (p.Leu146Ile)
c.805C>A (p.Leu269Ile)
19g.48750847C>ACA406703128FUT1c.435G>T (p.Gln145His)
c.804G>T (p.Gln268His)
19g.48750847C>GCA406703129FUT1c.435G>C (p.Gln145His)
c.804G>C (p.Gln268His)
19g.48750847C>TCA508274713FUT1c.435G>A (p.Gln145=)
c.804G>A (p.Gln268=)
19g.48750848T>ACA406703132FUT1c.434A>T (p.Gln145Leu)
c.803A>T (p.Gln268Leu)
19g.48750848T>CCA406703131FUT1c.434A>G (p.Gln145Arg)
c.803A>G (p.Gln268Arg)
gnomAD v4
19g.48750848T>GCA406703130FUT1c.434A>C (p.Gln145Pro)
c.803A>C (p.Gln268Pro)
19g.48750849G>ACA406703133FUT1c.433C>T (p.Gln145Ter)
c.802C>T (p.Gln268Ter)
19g.48750849G>CCA406703134FUT1c.433C>G (p.Gln145Glu)
c.802C>G (p.Gln268Glu)
19g.48750849G>TCA406703135FUT1c.433C>A (p.Gln145Lys)
c.802C>A (p.Gln268Lys)
19g.48750850C>ACA508274716FUT1c.432G>T (p.Leu144=)
c.801G>T (p.Leu267=)
19g.48750850C=CA2340053020FUT1c.432G= (p.Leu144=)
c.801G= (p.Leu267=)
19g.48750850C>GCA508274718FUT1c.432G>C (p.Leu144=)
c.801G>C (p.Leu267=)
19g.48750850C>TCA508274720FUT1c.432G>A (p.Leu144=)
c.801G>A (p.Leu267=)
dbSNP gnomAD v4
19g.48750851A>CCA406703136FUT1c.431T>G (p.Leu144Arg)
c.800T>G (p.Leu267Arg)
19g.48750851A>GCA406703137FUT1c.431T>C (p.Leu144Pro)
c.800T>C (p.Leu267Pro)
gnomAD v4
19g.48750851A>TCA406703138FUT1c.431T>A (p.Leu144Gln)
c.800T>A (p.Leu267Gln)
19g.48750852G>ACA508274722FUT1c.430C>T (p.Leu144=)
c.799C>T (p.Leu267=)
dbSNP gnomAD v4
19g.48750852G>CCA406703139FUT1c.430C>G (p.Leu144Val)
c.799C>G (p.Leu267Val)
19g.48750852G=CA2340053021FUT1c.430C= (p.Leu144=)
c.799C= (p.Leu267=)
19g.48750852G>TCA406703140FUT1c.430C>A (p.Leu144Met)
c.799C>A (p.Leu267Met)
19g.48750853C>ACA406703141FUT1c.429G>T (p.Glu143Asp)
c.798G>T (p.Glu266Asp)
19g.48750853C=CA2340053023FUT1c.429G= (p.Glu143=)
c.798G= (p.Glu266=)
19g.48750853C>GCA406703142FUT1c.429G>C (p.Glu143Asp)
c.798G>C (p.Glu266Asp)
gnomAD v4
19g.48750853C>TCA508274723FUT1c.429G>A (p.Glu143=)
c.798G>A (p.Glu266=)
dbSNP gnomAD v2 gnomAD v4
19g.48750854delCA645607137FUT1c.428del (p.Glu143GlyfsTer15)
c.797del (p.Glu266GlyfsTer15)
COSMIC
19g.48750854T>ACA406703143FUT1c.428A>T (p.Glu143Val)
c.797A>T (p.Glu266Val)
19g.48750854T>CCA406703144FUT1c.428A>G (p.Glu143Gly)
c.797A>G (p.Glu266Gly)
dbSNP gnomAD v4
19g.48750854T>GCA406703145FUT1c.428A>C (p.Glu143Ala)
c.797A>C (p.Glu266Ala)
19g.48750854T=CA2340053025FUT1c.428A= (p.Glu143=)
c.797A= (p.Glu266=)
19g.48750855C>ACA406703146FUT1c.427G>T (p.Glu143Ter)
c.796G>T (p.Glu266Ter)
19g.48750855C>GCA406703148FUT1c.427G>C (p.Glu143Gln)
c.796G>C (p.Glu266Gln)
19g.48750855C>TCA406703147FUT1c.427G>A (p.Glu143Lys)
c.796G>A (p.Glu266Lys)
19g.48750856C>ACA508274728FUT1c.426G>T (p.Arg142=)
c.795G>T (p.Arg265=)
19g.48750856C>GCA508274729FUT1c.426G>C (p.Arg142=)
c.795G>C (p.Arg265=)
19g.48750856C>TCA508274730FUT1c.426G>A (p.Arg142=)
c.795G>A (p.Arg265=)
19g.48750857C>ACA406703149FUT1c.425G>T (p.Arg142Leu)
c.794G>T (p.Arg265Leu)
COSMIC
19g.48750857C=CA2340053028FUT1c.425G= (p.Arg142=)
c.794G= (p.Arg265=)
19g.48750857C>GCA406703150FUT1c.425G>C (p.Arg142Pro)
c.794G>C (p.Arg265Pro)
19g.48750857C>TCA9557747FUT1c.425G>A (p.Arg142Gln)
c.794G>A (p.Arg265Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.48750858G>ACA9557748FUT1c.424C>T (p.Arg142Trp)
c.793C>T (p.Arg265Trp)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.48750858G>CCA406703151FUT1c.424C>G (p.Arg142Gly)
c.793C>G (p.Arg265Gly)
19g.48750858G=CA2340053031FUT1c.424C= (p.Arg142=)
c.793C= (p.Arg265=)
19g.48750858G>TCA508274732FUT1c.424C>A (p.Arg142=)
c.793C>A (p.Arg265=)
dbSNP
19g.48750859C>ACA406703152FUT1c.423G>T (p.Trp141Cys)
c.792G>T (p.Trp264Cys)
19g.48750859C=CA2340053034FUT1c.423G= (p.Trp141=)
c.792G= (p.Trp264=)
19g.48750859C>GCA406703153FUT1c.423G>C (p.Trp141Cys)
c.792G>C (p.Trp264Cys)
19g.48750859C>TCA406703154FUT1c.423G>A (p.Trp141Ter)
c.792G>A (p.Trp264Ter)
dbSNP
19g.48750860C>ACA406703155FUT1c.422G>T (p.Trp141Leu)
c.791G>T (p.Trp264Leu)
19g.48750860C=CA2340053037FUT1c.422G= (p.Trp141=)
c.791G= (p.Trp264=)
19g.48750860C>GCA406703156FUT1c.422G>C (p.Trp141Ser)
c.791G>C (p.Trp264Ser)
19g.48750860C>TCA9557749FUT1c.422G>A (p.Trp141Ter)
c.791G>A (p.Trp264Ter)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.48750861A>CCA406703158FUT1c.421T>G (p.Trp141Gly)
c.790T>G (p.Trp264Gly)
19g.48750861A>GCA406703159FUT1c.421T>C (p.Trp141Arg)
c.790T>C (p.Trp264Arg)
19g.48750861A>TCA406703157FUT1c.421T>A (p.Trp141Arg)
c.790T>A (p.Trp264Arg)
19g.48750862C>ACA508274734FUT1c.420G>T (p.Pro140=)
c.789G>T (p.Pro263=)
19g.48750862C=CA2340053044FUT1c.420G= (p.Pro140=)
c.789G= (p.Pro263=)
19g.48750862C>GCA508274735FUT1c.420G>C (p.Pro140=)
c.789G>C (p.Pro263=)
19g.48750862C>TCA508274737FUT1c.420G>A (p.Pro140=)
c.789G>A (p.Pro263=)
dbSNP gnomAD v3 gnomAD v4
19g.48750863G>ACA9557750FUT1c.419C>T (p.Pro140Leu)
c.788C>T (p.Pro263Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.48750863G>CCA9557751FUT1c.419C>G (p.Pro140Arg)
c.788C>G (p.Pro263Arg)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.48750863G=CA2340053047FUT1c.419C= (p.Pro140=)
c.788C= (p.Pro263=)
19g.48750863G>TCA406703160FUT1c.419C>A (p.Pro140Gln)
c.788C>A (p.Pro263Gln)
gnomAD v4
19g.48750864G>ACA9557752FUT1c.418C>T (p.Pro140Ser)
c.787C>T (p.Pro263Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.48750864G>CCA406703161FUT1c.418C>G (p.Pro140Ala)
c.787C>G (p.Pro263Ala)
gnomAD v4
19g.48750864G=CA2340053050FUT1c.418C= (p.Pro140=)
c.787C= (p.Pro263=)
19g.48750864G>TCA406703162FUT1c.418C>A (p.Pro140Thr)
c.787C>A (p.Pro263Thr)
19g.48750865delCA2576841995FUT1c.417del (p.Pro140ArgfsTer18)
c.786del (p.Pro263ArgfsTer18)
gnomAD v4
19g.48750865C>ACA508274738FUT1c.417G>T (p.Thr139=)
c.786G>T (p.Thr262=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.48750865C=CA2340053054FUT1c.417G= (p.Thr139=)
c.786G= (p.Thr262=)
19g.48750865C>GCA9557753FUT1c.417G>C (p.Thr139=)
c.786G>C (p.Thr262=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.48750865C>TCA508274740FUT1c.417G>A (p.Thr139=)
c.786G>A (p.Thr262=)
COSMIC
19g.48750866G>ACA406703163FUT1c.416C>T (p.Thr139Met)
c.785C>T (p.Thr262Met)
dbSNP gnomAD v4 COSMIC
19g.48750866G>CCA406703164FUT1c.416C>G (p.Thr139Arg)
c.785C>G (p.Thr262Arg)
19g.48750866G=CA2340053056FUT1c.416C= (p.Thr139=)
c.785C= (p.Thr262=)
19g.48750866G>TCA406703165FUT1c.416C>A (p.Thr139Lys)
c.785C>A (p.Thr262Lys)
19g.48750867T>ACA406703166FUT1c.415A>T (p.Thr139Ser)
c.784A>T (p.Thr262Ser)
19g.48750867T>CCA406703167FUT1c.415A>G (p.Thr139Ala)
c.784A>G (p.Thr262Ala)
dbSNP gnomAD v2 gnomAD v4
19g.48750867T>GCA406703168FUT1c.415A>C (p.Thr139Pro)
c.784A>C (p.Thr262Pro)
19g.48750867T=CA2340053058FUT1c.415A= (p.Thr139=)
c.784A= (p.Thr262=)
19g.48750868G>ACA508274742FUT1c.414C>T (p.Arg138=)
c.783C>T (p.Arg261=)
19g.48750868G>CCA508274743FUT1c.414C>G (p.Arg138=)
c.783C>G (p.Arg261=)
19g.48750868G>TCA508274744FUT1c.414C>A (p.Arg138=)
c.783C>A (p.Arg261=)
19g.48750869C>ACA406703169FUT1c.413G>T (p.Arg138Leu)
c.782G>T (p.Arg261Leu)
19g.48750869C=CA2340053062FUT1c.413G= (p.Arg138=)
c.782G= (p.Arg261=)
19g.48750869C>GCA406703170FUT1c.413G>C (p.Arg138Pro)
c.782G>C (p.Arg261Pro)
19g.48750869C>TCA406703171FUT1c.413G>A (p.Arg138His)
c.782G>A (p.Arg261His)
dbSNP
19g.48750870G>ACA9557754FUT1c.412C>T (p.Arg138Cys)
c.781C>T (p.Arg261Cys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.48750870G>CCA406703173FUT1c.412C>G (p.Arg138Gly)
c.781C>G (p.Arg261Gly)
19g.48750870G=CA2340053063FUT1c.412C= (p.Arg138=)
c.781C= (p.Arg261=)
19g.48750870G>TCA406703172FUT1c.412C>A (p.Arg138Ser)
c.781C>A (p.Arg261Ser)
19g.48750871G>ACA508274748FUT1c.411C>T (p.Ser137=)
c.780C>T (p.Ser260=)
19g.48750871G>CCA406703174FUT1c.411C>G (p.Ser137Arg)
c.780C>G (p.Ser260Arg)
19g.48750871G=CA2340053065FUT1c.411C= (p.Ser137=)
c.780C= (p.Ser260=)
19g.48750871G>TCA9557755FUT1c.411C>A (p.Ser137Arg)
c.780C>A (p.Ser260Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.48750872C>ACA406703175FUT1c.410G>T (p.Ser137Ile)
c.779G>T (p.Ser260Ile)
19g.48750872C>GCA406703176FUT1c.410G>C (p.Ser137Thr)
c.779G>C (p.Ser260Thr)
19g.48750872C>TCA406703177FUT1c.410G>A (p.Ser137Asn)
c.779G>A (p.Ser260Asn)
19g.48750873T>ACA406703178FUT1c.409A>T (p.Ser137Cys)
c.778A>T (p.Ser260Cys)
19g.48750873T>CCA406703179FUT1c.409A>G (p.Ser137Gly)
c.778A>G (p.Ser260Gly)
19g.48750873T>GCA406703180FUT1c.409A>C (p.Ser137Arg)
c.778A>C (p.Ser260Arg)
19g.48750874G>ACA508274751FUT1c.408C>T (p.Asp136=)
c.777C>T (p.Asp259=)
19g.48750874G>CCA406703181FUT1c.408C>G (p.Asp136Glu)
c.777C>G (p.Asp259Glu)
gnomAD v4
19g.48750874G>TCA406703182FUT1c.408C>A (p.Asp136Glu)
c.777C>A (p.Asp259Glu)
19g.48750874_48750875delinsGTCA2340053067FUT1c.407_408delinsAC (p.Asp136=)
c.776_777delinsAC (p.Asp259=)
19g.48750875delCA9557756FUT1c.407del (p.Asp136AlafsTer22)
c.776del (p.Asp259AlafsTer22)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.48750875T>ACA406703184FUT1c.407A>T (p.Asp136Val)
c.776A>T (p.Asp259Val)
19g.48750875T>CCA406703185FUT1c.407A>G (p.Asp136Gly)
c.776A>G (p.Asp259Gly)
19g.48750875T>GCA406703183FUT1c.407A>C (p.Asp136Ala)
c.776A>C (p.Asp259Ala)
19g.48750876C>ACA406703186FUT1c.406G>T (p.Asp136Tyr)
c.775G>T (p.Asp259Tyr)
19g.48750876C>GCA406703187FUT1c.406G>C (p.Asp136His)
c.775G>C (p.Asp259His)
19g.48750876C>TCA406703188FUT1c.406G>A (p.Asp136Asn)
c.775G>A (p.Asp259Asn)
19g.48750877C>ACA508274754FUT1c.405G>T (p.Val135=)
c.774G>T (p.Val258=)
19g.48750877C>GCA508274755FUT1c.405G>C (p.Val135=)
c.774G>C (p.Val258=)
19g.48750877C>TCA508274756FUT1c.405G>A (p.Val135=)
c.774G>A (p.Val258=)
19g.48750878A=CA2340053070FUT1c.404T= (p.Val135=)
c.773T= (p.Val258=)
19g.48750878A>CCA406703189FUT1c.404T>G (p.Val135Gly)
c.773T>G (p.Val258Gly)
19g.48750878A>GCA406703190FUT1c.404T>C (p.Val135Ala)
c.773T>C (p.Val258Ala)
dbSNP
19g.48750878A>TCA309358458FUT1c.404T>A (p.Val135Glu)
c.773T>A (p.Val258Glu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.48750879C>ACA406703191FUT1c.403G>T (p.Val135Leu)
c.772G>T (p.Val258Leu)
19g.48750879C>GCA406703192FUT1c.403G>C (p.Val135Leu)
c.772G>C (p.Val258Leu)
19g.48750879C>TCA406703193FUT1c.403G>A (p.Val135Met)
c.772G>A (p.Val258Met)
gnomAD v4
19g.48750880T>ACA406703194FUT1c.402A>T (p.Glu134Asp)
c.771A>T (p.Glu257Asp)
19g.48750880T>CCA508274758FUT1c.402A>G (p.Glu134=)
c.771A>G (p.Glu257=)
19g.48750880T>GCA9557757FUT1c.402A>C (p.Glu134Asp)
c.771A>C (p.Glu257Asp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.48750880T=CA2340053073FUT1c.402A= (p.Glu134=)
c.771A= (p.Glu257=)
19g.48750881T>ACA406703196FUT1c.401A>T (p.Glu134Val)
c.770A>T (p.Glu257Val)
19g.48750881T>CCA406703197FUT1c.401A>G (p.Glu134Gly)
c.770A>G (p.Glu257Gly)
19g.48750881T>GCA406703195FUT1c.401A>C (p.Glu134Ala)
c.770A>C (p.Glu257Ala)
19g.48750882C>ACA406703198FUT1c.400G>T (p.Glu134Ter)
c.769G>T (p.Glu257Ter)
19g.48750882C>GCA406703199FUT1c.400G>C (p.Glu134Gln)
c.769G>C (p.Glu257Gln)
19g.48750882C>TCA406703200FUT1c.400G>A (p.Glu134Lys)
c.769G>A (p.Glu257Lys)
19g.48750883T>ACA508274762FUT1c.399A>T (p.Pro133=)
c.768A>T (p.Pro256=)
19g.48750883T>CCA508274764FUT1c.399A>G (p.Pro133=)
c.768A>G (p.Pro256=)
dbSNP gnomAD v4
19g.48750883T>GCA508274765FUT1c.399A>C (p.Pro133=)
c.768A>C (p.Pro256=)
19g.48750883T=CA2340053076FUT1c.399A= (p.Pro133=)
c.768A= (p.Pro256=)
19g.48750883_48750886delinsTGGGCA2340053075FUT1c.396_399delinsCCCA (p.Ala132=)
c.765_768delinsCCCA (p.Ala255=)
19g.48750884G>ACA406703203FUT1c.398C>T (p.Pro133Leu)
c.767C>T (p.Pro256Leu)
19g.48750884G>CCA406703202FUT1c.398C>G (p.Pro133Arg)
c.767C>G (p.Pro256Arg)
19g.48750884G>TCA406703201FUT1c.398C>A (p.Pro133Gln)
c.767C>A (p.Pro256Gln)
19g.48750885_48750887delCA9557758FUT1c.396_398del (p.Pro133del)
c.765_767del (p.Pro256del)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.48750892_48750924delCA2695228998FUT1c.366_398del (p.Val123_Pro133del)
c.735_767del (p.Val246_Pro256del)
19g.48750885G>ACA406703204FUT1c.397C>T (p.Pro133Ser)
c.766C>T (p.Pro256Ser)
19g.48750885G>CCA406703205FUT1c.397C>G (p.Pro133Ala)
c.766C>G (p.Pro256Ala)
19g.48750885G>TCA406703206FUT1c.397C>A (p.Pro133Thr)
c.766C>A (p.Pro256Thr)
19g.48750886G>ACA508274770FUT1c.396C>T (p.Ala132=)
c.765C>T (p.Ala255=)
19g.48750886G>CCA508274771FUT1c.396C>G (p.Ala132=)
c.765C>G (p.Ala255=)
19g.48750886G>TCA508274772FUT1c.396C>A (p.Ala132=)
c.765C>A (p.Ala255=)
19g.48750887G>ACA309358472FUT1c.395C>T (p.Ala132Val)
c.764C>T (p.Ala255Val)
dbSNP gnomAD v4
19g.48750887G>CCA406703207FUT1c.395C>G (p.Ala132Gly)
c.764C>G (p.Ala255Gly)
19g.48750887G=CA2340053079FUT1c.395C= (p.Ala132=)
c.764C= (p.Ala255=)
19g.48750887G>TCA406703208FUT1c.395C>A (p.Ala132Asp)
c.764C>A (p.Ala255Asp)
19g.48750888C>ACA406703211FUT1c.394G>T (p.Ala132Ser)
c.763G>T (p.Ala255Ser)
gnomAD v4
19g.48750888C>GCA406703210FUT1c.394G>C (p.Ala132Pro)
c.763G>C (p.Ala255Pro)
gnomAD v4
19g.48750888C>TCA406703209FUT1c.394G>A (p.Ala132Thr)
c.763G>A (p.Ala255Thr)
gnomAD v4
19g.48750889C>ACA508274775FUT1c.393G>T (p.Leu131=)
c.762G>T (p.Leu254=)
19g.48750889C>GCA508274776FUT1c.393G>C (p.Leu131=)
c.762G>C (p.Leu254=)
19g.48750889C>TCA508274774FUT1c.393G>A (p.Leu131=)
c.762G>A (p.Leu254=)
COSMIC
19g.48750890A>CCA406703212FUT1c.392T>G (p.Leu131Arg)
c.761T>G (p.Leu254Arg)
19g.48750890A>GCA406703214FUT1c.392T>C (p.Leu131Pro)
c.761T>C (p.Leu254Pro)
19g.48750890A>TCA406703213FUT1c.392T>A (p.Leu131Gln)
c.761T>A (p.Leu254Gln)
19g.48750891G>ACA508274777FUT1c.391C>T (p.Leu131=)
c.760C>T (p.Leu254=)
19g.48750891G>CCA406703215FUT1c.391C>G (p.Leu131Val)
c.760C>G (p.Leu254Val)
19g.48750891G>TCA406703216FUT1c.391C>A (p.Leu131Met)
c.760C>A (p.Leu254Met)

Number of alleles fetched