Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.18596717T>ACA404850621CRLF1c.929A>T (p.Gln310Leu)
c.394A>T
c.863A>T (p.Gln288Leu)
19g.18596717T>CCA404850622CRLF1c.929A>G (p.Gln310Arg)
c.394A>G
c.863A>G (p.Gln288Arg)
19g.18596717T>GCA404850623CRLF1c.929A>C (p.Gln310Pro)
c.394A>C
c.863A>C (p.Gln288Pro)
19g.18596718G>ACA404850626CRLF1c.928C>T (p.Gln310Ter)
c.393C>T
c.862C>T (p.Gln288Ter)
19g.18596718G>CCA404850624CRLF1c.928C>G (p.Gln310Glu)
c.393C>G
c.862C>G (p.Gln288Glu)
19g.18596718G>TCA404850625CRLF1c.928C>A (p.Gln310Lys)
c.393C>A
c.862C>A (p.Gln288Lys)
19g.18596719C>ACA506116361CRLF1c.927G>T (p.Val309=)
c.392G>T
c.861G>T (p.Val287=)
dbSNP
19g.18596719C=CA2326432270CRLF1c.927G= (p.Val309=)
c.392G=
c.861G= (p.Val287=)
19g.18596719C>GCA506116363CRLF1c.927G>C (p.Val309=)
c.392G>C
c.861G>C (p.Val287=)
19g.18596719C>TCA506116365CRLF1c.927G>A (p.Val309=)
c.392G>A
c.861G>A (p.Val287=)
19g.18596720A=CA2326432271CRLF1c.926T= (p.Val309=)
c.391T=
c.860T= (p.Val287=)
19g.18596720A>CCA404850627CRLF1c.926T>G (p.Val309Gly)
c.391T>G
c.860T>G (p.Val287Gly)
19g.18596720A>GCA404850628CRLF1c.926T>C (p.Val309Ala)
c.391T>C
c.860T>C (p.Val287Ala)
dbSNP gnomAD v2 gnomAD v4
19g.18596720A>TCA404850629CRLF1c.926T>A (p.Val309Glu)
c.391T>A
c.860T>A (p.Val287Glu)
19g.18596721C>ACA306260329CRLF1c.925G>T (p.Val309Leu)
c.390G>T
c.859G>T (p.Val287Leu)
dbSNP gnomAD v3 gnomAD v4
19g.18596721C=CA2326432272CRLF1c.925G= (p.Val309=)
c.390G=
c.859G= (p.Val287=)
19g.18596721C>GCA404850630CRLF1c.925G>C (p.Val309Leu)
c.390G>C
c.859G>C (p.Val287Leu)
19g.18596721C>TCA404850631CRLF1c.925G>A (p.Val309Met)
c.390G>A
c.859G>A (p.Val287Met)
dbSNP gnomAD v2 gnomAD v4
19g.18596722G>ACA506116367CRLF1c.924C>T (p.Phe308=)
c.389C>T
c.858C>T (p.Phe286=)
dbSNP gnomAD v3 gnomAD v4
19g.18596722G>CCA404850632CRLF1c.924C>G (p.Phe308Leu)
c.389C>G
c.858C>G (p.Phe286Leu)
19g.18596722G=CA2326432273CRLF1c.924C= (p.Phe308=)
c.389C=
c.858C= (p.Phe286=)
19g.18596722G>TCA404850633CRLF1c.924C>A (p.Phe308Leu)
c.389C>A
c.858C>A (p.Phe286Leu)
dbSNP gnomAD v2 gnomAD v4
19g.18596722dupCA2583602660CRLF1c.924dup (p.Val309ArgfsTer21)
c.389dup
c.858dup (p.Val287ArgfsTer21)
gnomAD v4
19g.18596723A>CCA404850634CRLF1c.923T>G (p.Phe308Cys)
c.388T>G
c.857T>G (p.Phe286Cys)
19g.18596723A>GCA404850636CRLF1c.923T>C (p.Phe308Ser)
c.388T>C
c.857T>C (p.Phe286Ser)
19g.18596723A>TCA404850635CRLF1c.923T>A (p.Phe308Tyr)
c.388T>A
c.857T>A (p.Phe286Tyr)
19g.18596724A=CA2326432274CRLF1c.922T= (p.Phe308=)
c.387T=
c.856T= (p.Phe286=)
19g.18596724A>CCA404850637CRLF1c.922T>G (p.Phe308Val)
c.387T>G
c.856T>G (p.Phe286Val)
gnomAD v4
19g.18596724A>GCA404850639CRLF1c.922T>C (p.Phe308Leu)
c.387T>C
c.856T>C (p.Phe286Leu)
dbSNP gnomAD v4
19g.18596724A>TCA404850638CRLF1c.922T>A (p.Phe308Ile)
c.387T>A
c.856T>A (p.Phe286Ile)
19g.18596725G>ACA506116368CRLF1c.921C>T (p.Tyr307=)
c.386C>T
c.855C>T (p.Tyr285=)
19g.18596725G>CCA404850640CRLF1c.921C>G (p.Tyr307Ter)
c.386C>G
c.855C>G (p.Tyr285Ter)
19g.18596725G>TCA404850641CRLF1c.921C>A (p.Tyr307Ter)
c.386C>A
c.855C>A (p.Tyr285Ter)
19g.18596726T>ACA404850642CRLF1c.920A>T (p.Tyr307Phe)
c.385A>T
c.854A>T (p.Tyr285Phe)
19g.18596726T>CCA404850644CRLF1c.920A>G (p.Tyr307Cys)
c.385A>G
c.854A>G (p.Tyr285Cys)
19g.18596726T>GCA404850643CRLF1c.920A>C (p.Tyr307Ser)
c.385A>C
c.854A>C (p.Tyr285Ser)
19g.18596727A>CCA404850645CRLF1c.919T>G (p.Tyr307Asp)
c.384T>G
c.853T>G (p.Tyr285Asp)
19g.18596727A>GCA404850646CRLF1c.919T>C (p.Tyr307His)
c.384T>C
c.853T>C (p.Tyr285His)
gnomAD v4
19g.18596727A>TCA404850647CRLF1c.919T>A (p.Tyr307Asn)
c.384T>A
c.853T>A (p.Tyr285Asn)
19g.18596728C>ACA506116370CRLF1c.918G>T (p.Val306=)
c.383G>T
c.852G>T (p.Val284=)
19g.18596728C>GCA506116372CRLF1c.918G>C (p.Val306=)
c.383G>C
c.852G>C (p.Val284=)
gnomAD v4
19g.18596728C>TCA506116371CRLF1c.918G>A (p.Val306=)
c.383G>A
c.852G>A (p.Val284=)
19g.18596729A>CCA404850648CRLF1c.917T>G (p.Val306Gly)
c.382T>G
c.851T>G (p.Val284Gly)
19g.18596729A>GCA404850649CRLF1c.917T>C (p.Val306Ala)
c.382T>C
c.851T>C (p.Val284Ala)
COSMIC
19g.18596729A>TCA404850650CRLF1c.917T>A (p.Val306Glu)
c.382T>A
c.851T>A (p.Val284Glu)
19g.18596730C>ACA404850651CRLF1c.916G>T (p.Val306Leu)
c.381G>T
c.850G>T (p.Val284Leu)
dbSNP gnomAD v4
19g.18596730C=CA2326432275CRLF1c.916G= (p.Val306=)
c.381G=
c.850G= (p.Val284=)
19g.18596730C>GCA404850652CRLF1c.916G>C (p.Val306Leu)
c.381G>C
c.850G>C (p.Val284Leu)
dbSNP gnomAD v2 gnomAD v4
19g.18596730C>TCA9314050CRLF1c.916G>A (p.Val306Met)
c.381G>A
c.850G>A (p.Val284Met)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.18596731G>ACA506116373CRLF1c.915C>T (p.Thr305=)
c.380C>T
c.849C>T (p.Thr283=)
gnomAD v4
19g.18596731G>CCA506116374CRLF1c.915C>G (p.Thr305=)
c.380C>G
c.849C>G (p.Thr283=)
gnomAD v4
19g.18596731G>TCA506116375CRLF1c.915C>A (p.Thr305=)
c.380C>A
c.849C>A (p.Thr283=)
dbSNP
19g.18596732G>ACA404850653CRLF1c.914C>T (p.Thr305Ile)
c.379C>T
c.848C>T (p.Thr283Ile)
19g.18596732G>CCA404850654CRLF1c.914C>G (p.Thr305Ser)
c.379C>G
c.848C>G (p.Thr283Ser)
19g.18596732G>TCA404850655CRLF1c.914C>A (p.Thr305Asn)
c.379C>A
c.848C>A (p.Thr283Asn)
19g.18596733T>ACA404850658CRLF1c.913A>T (p.Thr305Ser)
c.378A>T
c.847A>T (p.Thr283Ser)
19g.18596733T>CCA404850656CRLF1c.913A>G (p.Thr305Ala)
c.378A>G
c.847A>G (p.Thr283Ala)
19g.18596733T>GCA404850657CRLF1c.913A>C (p.Thr305Pro)
c.378A>C
c.847A>C (p.Thr283Pro)
19g.18596734G>ACA506116376CRLF1c.912C>T (p.Gly304=)
c.377C>T
c.846C>T (p.Gly282=)
19g.18596734G>CCA506116377CRLF1c.912C>G (p.Gly304=)
c.377C>G
c.846C>G (p.Gly282=)
19g.18596734G=CA2326432276CRLF1c.912C= (p.Gly304=)
c.377C=
c.846C= (p.Gly282=)
19g.18596734G>TCA9314051CRLF1c.912C>A (p.Gly304=)
c.377C>A
c.846C>A (p.Gly282=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.18596735C>ACA404850659CRLF1c.911G>T (p.Gly304Val)
c.376G>T
c.845G>T (p.Gly282Val)
19g.18596735C>GCA404850660CRLF1c.911G>C (p.Gly304Ala)
c.376G>C
c.845G>C (p.Gly282Ala)
19g.18596735C>TCA404850661CRLF1c.911G>A (p.Gly304Asp)
c.376G>A
c.845G>A (p.Gly282Asp)
19g.18596736C>ACA404850662CRLF1c.910G>T (p.Gly304Cys)
c.375G>T
c.844G>T (p.Gly282Cys)
19g.18596736C=CA2326432277CRLF1c.910G= (p.Gly304=)
c.375G=
c.844G= (p.Gly282=)
19g.18596736C>GCA9314052CRLF1c.910G>C (p.Gly304Arg)
c.375G>C
c.844G>C (p.Gly282Arg)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.18596736C>TCA306260340CRLF1c.910G>A (p.Gly304Ser)
c.375G>A
c.844G>A (p.Gly282Ser)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.18596736_18596738delinsCGGCA2326432278CRLF1c.908_910delinsCCG (p.Pro303=)
c.373_375delinsCCG
c.842_844delinsCCG (p.Pro281=)
19g.18596737G>ACA506116381CRLF1c.909C>T (p.Pro303=)
c.374C>T
c.843C>T (p.Pro281=)
dbSNP gnomAD v4
19g.18596737G>CCA506116382CRLF1c.909C>G (p.Pro303=)
c.374C>G
c.843C>G (p.Pro281=)
19g.18596737G=CA2326432280CRLF1c.909C= (p.Pro303=)
c.374C=
c.843C= (p.Pro281=)
19g.18596737G>TCA506116383CRLF1c.909C>A (p.Pro303=)
c.374C>A
c.843C>A (p.Pro281=)
19g.18596739delCA2583602691CRLF1c.909del (p.Gly304AlafsTer?)
c.374del
c.843del (p.Gly282AlafsTer?)
gnomAD v4
19g.18596738_18596739delCA2326432279CRLF1c.908_909del (p.Pro303ArgfsTer26)
c.373_374del
c.842_843del (p.Pro281ArgfsTer26)
dbSNP
19g.18596738G>ACA404850663CRLF1c.908C>T (p.Pro303Leu)
c.373C>T
c.842C>T (p.Pro281Leu)
gnomAD v4
19g.18596738G>CCA404850664CRLF1c.908C>G (p.Pro303Arg)
c.373C>G
c.842C>G (p.Pro281Arg)
gnomAD v4
19g.18596738G>TCA404850665CRLF1c.908C>A (p.Pro303His)
c.373C>A
c.842C>A (p.Pro281His)
19g.18596739G>ACA404850668CRLF1c.907C>T (p.Pro303Ser)
c.372C>T
c.841C>T (p.Pro281Ser)
gnomAD v4
19g.18596739G>CCA404850667CRLF1c.907C>G (p.Pro303Ala)
c.372C>G
c.841C>G (p.Pro281Ala)
19g.18596739G>TCA404850666CRLF1c.907C>A (p.Pro303Thr)
c.372C>A
c.841C>A (p.Pro281Thr)
19g.18596740T>ACA404850669CRLF1c.906A>T (p.Lys302Asn)
c.371A>T
c.840A>T (p.Lys280Asn)
19g.18596740T>CCA506116385CRLF1c.906A>G (p.Lys302=)
c.371A>G
c.840A>G (p.Lys280=)
19g.18596740T>GCA404850670CRLF1c.906A>C (p.Lys302Asn)
c.371A>C
c.840A>C (p.Lys280Asn)
19g.18596741T>ACA404850671CRLF1c.905A>T (p.Lys302Ile)
c.370A>T
c.839A>T (p.Lys280Ile)
19g.18596741T>CCA404850672CRLF1c.905A>G (p.Lys302Arg)
c.370A>G
c.839A>G (p.Lys280Arg)
19g.18596741T>GCA404850673CRLF1c.905A>C (p.Lys302Thr)
c.370A>C
c.839A>C (p.Lys280Thr)
19g.18596742T>ACA404850674CRLF1c.904A>T (p.Lys302Ter)
c.369A>T
c.838A>T (p.Lys280Ter)
19g.18596742T>CCA404850675CRLF1c.904A>G (p.Lys302Glu)
c.369A>G
c.838A>G (p.Lys280Glu)
19g.18596742T>GCA9314053CRLF1c.904A>C (p.Lys302Gln)
c.369A>C
c.838A>C (p.Lys280Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.18596742T=CA2326432281CRLF1c.904A= (p.Lys302=)
c.369A=
c.838A= (p.Lys280=)
19g.18596743C>ACA506116389CRLF1c.903G>T (p.Leu301=)
c.368G>T
c.837G>T (p.Leu279=)
19g.18596743C=CA2326432282CRLF1c.903G= (p.Leu301=)
c.368G=
c.837G= (p.Leu279=)
19g.18596743C>GCA9314054CRLF1c.903G>C (p.Leu301=)
c.368G>C
c.837G>C (p.Leu279=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.18596743C>TCA506116388CRLF1c.903G>A (p.Leu301=)
c.368G>A
c.837G>A (p.Leu279=)
dbSNP gnomAD v2
19g.18596744A>CCA404850676CRLF1c.902T>G (p.Leu301Arg)
c.367T>G
c.836T>G (p.Leu279Arg)
19g.18596744A>GCA404850677CRLF1c.902T>C (p.Leu301Pro)
c.367T>C
c.836T>C (p.Leu279Pro)
19g.18596744A>TCA404850678CRLF1c.902T>A (p.Leu301Gln)
c.367T>A
c.836T>A (p.Leu279Gln)
19g.18596745G>ACA506116391CRLF1c.901C>T (p.Leu301=)
c.366C>T
c.835C>T (p.Leu279=)
19g.18596745G>CCA404850679CRLF1c.901C>G (p.Leu301Val)
c.366C>G
c.835C>G (p.Leu279Val)
19g.18596745G>TCA404850680CRLF1c.901C>A (p.Leu301Met)
c.366C>A
c.835C>A (p.Leu279Met)
19g.18596746G>ACA506116394CRLF1c.900C>T (p.Gly300=)
c.365C>T
c.834C>T (p.Gly278=)
19g.18596746G>CCA506116395CRLF1c.900C>G (p.Gly300=)
c.365C>G
c.834C>G (p.Gly278=)
19g.18596746G=CA2326432283CRLF1c.900C= (p.Gly300=)
c.365C=
c.834C= (p.Gly278=)
19g.18596746G>TCA9314055CRLF1c.900C>A (p.Gly300=)
c.365C>A
c.834C>A (p.Gly278=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.18596747C>ACA404850681CRLF1c.899G>T (p.Gly300Val)
c.364G>T
c.833G>T (p.Gly278Val)
gnomAD v4
19g.18596747C>GCA404850682CRLF1c.899G>C (p.Gly300Ala)
c.364G>C
c.833G>C (p.Gly278Ala)
19g.18596747C>TCA404850683CRLF1c.899G>A (p.Gly300Asp)
c.364G>A
c.833G>A (p.Gly278Asp)
19g.18596748C>ACA404850684CRLF1c.898G>T (p.Gly300Cys)
c.363G>T
c.832G>T (p.Gly278Cys)
19g.18596748C=CA2326432284CRLF1c.898G= (p.Gly300=)
c.363G=
c.832G= (p.Gly278=)
19g.18596748C>GCA404850685CRLF1c.898G>C (p.Gly300Arg)
c.363G>C
c.832G>C (p.Gly278Arg)
gnomAD v4
19g.18596748C>TCA404850686CRLF1c.898G>A (p.Gly300Ser)
c.363G>A
c.832G>A (p.Gly278Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.18596749G>ACA506116396CRLF1c.897C>T (p.Ala299=)
c.362C>T
c.831C>T (p.Ala277=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.18596749G>CCA506116397CRLF1c.897C>G (p.Ala299=)
c.362C>G
c.831C>G (p.Ala277=)
19g.18596749G=CA2326432285CRLF1c.897C= (p.Ala299=)
c.362C=
c.831C= (p.Ala277=)
19g.18596749G>TCA506116398CRLF1c.897C>A (p.Ala299=)
c.362C>A
c.831C>A (p.Ala277=)
gnomAD v4
19g.18596750G>ACA404850687CRLF1c.896C>T (p.Ala299Val)
c.361C>T
c.830C>T (p.Ala277Val)
19g.18596750G>CCA404850688CRLF1c.896C>G (p.Ala299Gly)
c.361C>G
c.830C>G (p.Ala277Gly)
19g.18596750G>TCA404850689CRLF1c.896C>A (p.Ala299Asp)
c.361C>A
c.830C>A (p.Ala277Asp)
19g.18596751C>ACA404850690CRLF1c.895G>T (p.Ala299Ser)
c.360G>T
c.829G>T (p.Ala277Ser)
19g.18596751C>GCA404850691CRLF1c.895G>C (p.Ala299Pro)
c.360G>C
c.829G>C (p.Ala277Pro)
19g.18596751C>TCA404850692CRLF1c.895G>A (p.Ala299Thr)
c.360G>A
c.829G>A (p.Ala277Thr)
19g.18596752C>ACA506116402CRLF1c.894G>T (p.Leu298=)
c.359G>T
c.828G>T (p.Leu276=)
19g.18596752C>GCA506116403CRLF1c.894G>C (p.Leu298=)
c.359G>C
c.828G>C (p.Leu276=)
19g.18596752C>TCA506116404CRLF1c.894G>A (p.Leu298=)
c.359G>A
c.828G>A (p.Leu276=)
19g.18596753A=CA2326432286CRLF1c.893T= (p.Leu298=)
c.358T=
c.827T= (p.Leu276=)
19g.18596753A>CCA404850695CRLF1c.893T>G (p.Leu298Arg)
c.358T>G
c.827T>G (p.Leu276Arg)
dbSNP
19g.18596753A>GCA404850694CRLF1c.893T>C (p.Leu298Pro)
c.358T>C
c.827T>C (p.Leu276Pro)
dbSNP gnomAD v2 gnomAD v4
19g.18596753A>TCA404850693CRLF1c.893T>A (p.Leu298Gln)
c.358T>A
c.827T>A (p.Leu276Gln)
19g.18596754G>ACA506116405CRLF1c.892C>T (p.Leu298=)
c.357C>T
c.826C>T (p.Leu276=)
19g.18596754G>CCA404850696CRLF1c.892C>G (p.Leu298Val)
c.357C>G
c.826C>G (p.Leu276Val)
19g.18596754G>TCA404850697CRLF1c.892C>A (p.Leu298Met)
c.357C>A
c.826C>A (p.Leu276Met)
19g.18596755G>ACA506116406CRLF1c.891C>T (p.Arg297=)
c.356C>T
c.825C>T (p.Arg275=)
19g.18596755G>CCA506116407CRLF1c.891C>G (p.Arg297=)
c.356C>G
c.825C>G (p.Arg275=)
19g.18596755G>TCA506116408CRLF1c.891C>A (p.Arg297=)
c.356C>A
c.825C>A (p.Arg275=)
19g.18596756C>ACA9314056CRLF1c.890G>T (p.Arg297Leu)
c.355G>T
c.824G>T (p.Arg275Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.18596756C=CA2326432287CRLF1c.890G= (p.Arg297=)
c.355G=
c.824G= (p.Arg275=)
19g.18596756C>GCA404850698CRLF1c.890G>C (p.Arg297Pro)
c.355G>C
c.824G>C (p.Arg275Pro)
19g.18596756C>TCA9314057CRLF1c.890G>A (p.Arg297His)
c.355G>A
c.824G>A (p.Arg275His)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.18596757G>ACA9314058CRLF1c.889C>T (p.Arg297Cys)
c.354C>T
c.823C>T (p.Arg275Cys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.18596757G>CCA404850699CRLF1c.889C>G (p.Arg297Gly)
c.354C>G
c.823C>G (p.Arg275Gly)
19g.18596757G=CA2326432288CRLF1c.889C= (p.Arg297=)
c.354C=
c.823C= (p.Arg275=)
19g.18596757G>TCA404850700CRLF1c.889C>A (p.Arg297Ser)
c.354C>A
c.823C>A (p.Arg275Ser)
19g.18596758G>ACA506116411CRLF1c.888C>T (p.Cys296=)
c.353C>T
c.822C>T (p.Cys274=)
19g.18596758G>CCA404850701CRLF1c.888C>G (p.Cys296Trp)
c.353C>G
c.822C>G (p.Cys274Trp)
19g.18596758G>TCA404850702CRLF1c.888C>A (p.Cys296Ter)
c.353C>A
c.822C>A (p.Cys274Ter)
COSMIC
19g.18596759C>ACA404850703CRLF1c.887G>T (p.Cys296Phe)
c.352G>T
c.821G>T (p.Cys274Phe)
19g.18596759C>GCA404850704CRLF1c.887G>C (p.Cys296Ser)
c.352G>C
c.821G>C (p.Cys274Ser)
19g.18596759C>TCA404850705CRLF1c.887G>A (p.Cys296Tyr)
c.352G>A
c.821G>A (p.Cys274Tyr)
19g.18596759_18596762delinsCAGGCA2326432289CRLF1c.884_887delinsCCTG (p.Ser295=)
c.349_352delinsCCTG
c.818_821delinsCCTG (p.Ser273=)
19g.18596760A>CCA404850706CRLF1c.886T>G (p.Cys296Gly)
c.351T>G
c.820T>G (p.Cys274Gly)
19g.18596760A>GCA404850707CRLF1c.886T>C (p.Cys296Arg)
c.351T>C
c.820T>C (p.Cys274Arg)
19g.18596760A>TCA404850708CRLF1c.886T>A (p.Cys296Ser)
c.351T>A
c.820T>A (p.Cys274Ser)
19g.18596763_18596765delCA994214130CRLF1c.884_886del (p.Ser295del)
c.349_351del
c.818_820del (p.Ser273del)
dbSNP gnomAD v3 gnomAD v4
19g.18596760_18596761insTTTGATGTCGCAGAATTTTTCCGCGCCCAAATCCGCGCCGAAGCCCGCTTCCA2526224994CRLF1c.885_886insGAAGCGGGCTTCGGCGCGGATTTGGGCGCGGAAAAATTCTGCGACATCAAA (p.Ser295_Cys296insGluAlaGlyPheGlyAlaAspLeuGlyAlaGluLysPheCysAspIleLys)
c.350_351insGAAGCGGGCTTCGGCGCGGATTTGGGCGCGGAAAAATTCTGCGACATCAAA
c.819_820insGAAGCGGGCTTCGGCGCGGATTTGGGCGCGGAAAAATTCTGCGACATCAAA (p.Ser273_Cys274insGluAlaGlyPheGlyAlaAspLeuGlyAlaGluLysPheCysAspIleLys)
19g.18596760_18596761insTTTGATGTCGCAGAATTTTTCCGCGCCCAAATCCGCGCCGAAACCCGCTTCGGTAACGGCATAATCGGCCAGATGCAGGGCGAGGCGGGTGGCGGTAACGGAGTTGCAGCCGTGGGCGATGTTGGCGAAGCA2558194762CRLF1c.885_886insCTTCGCCAACATCGCCCACGGCTGCAACTCCGTTACCGCCACCCGCCTCGCCCTGCATCTGGCCGATTATGCCGTTACCGAAGCGGGTTTCGGCGCGGATTTGGGCGCGGAAAAATTCTGCGACATCAAA (p.Cys296LeufsTer?)
c.350_351insCTTCGCCAACATCGCCCACGGCTGCAACTCCGTTACCGCCACCCGCCTCGCCCTGCATCTGGCCGATTATGCCGTTACCGAAGCGGGTTTCGGCGCGGATTTGGGCGCGGAAAAATTCTGCGACATCAAA
c.819_820insCTTCGCCAACATCGCCCACGGCTGCAACTCCGTTACCGCCACCCGCCTCGCCCTGCATCTGGCCGATTATGCCGTTACCGAAGCGGGTTTCGGCGCGGATTTGGGCGCGGAAAAATTCTGCGACATCAAA (p.Cys274LeufsTer?)
19g.18596761G>ACA306260370CRLF1c.885C>T (p.Ser295=)
c.350C>T
c.819C>T (p.Ser273=)
dbSNP gnomAD v4 COSMIC
19g.18596761G>CCA506116413CRLF1c.885C>G (p.Ser295=)
c.350C>G
c.819C>G (p.Ser273=)
19g.18596761G=CA2326432290CRLF1c.885C= (p.Ser295=)
c.350C=
c.819C= (p.Ser273=)
19g.18596761G>TCA506116415CRLF1c.885C>A (p.Ser295=)
c.350C>A
c.819C>A (p.Ser273=)
19g.18596762G>ACA404850709CRLF1c.884C>T (p.Ser295Phe)
c.349C>T
c.818C>T (p.Ser273Phe)
19g.18596762G>CCA404850710CRLF1c.884C>G (p.Ser295Cys)
c.349C>G
c.818C>G (p.Ser273Cys)
19g.18596762G>TCA404850711CRLF1c.884C>A (p.Ser295Tyr)
c.349C>A
c.818C>A (p.Ser273Tyr)
19g.18596762_18596763insTAACGGCATAATCGGCCAGATGCAGGGCGAGGCGGGTGGCGGTAACGGAGTTGCAGCCGTGGGCGATGTTGGCGACA2501863485CRLF1c.883_884insTCGCCAACATCGCCCACGGCTGCAACTCCGTTACCGCCACCCGCCTCGCCCTGCATCTGGCCGATTATGCCGTTA (p.Ser295delinsPheAlaAsnIleAlaHisGlyCysAsnSerValThrAlaThrArgLeuAlaLeuHisLeuAlaAspTyrAlaValThr)
c.348_349insTCGCCAACATCGCCCACGGCTGCAACTCCGTTACCGCCACCCGCCTCGCCCTGCATCTGGCCGATTATGCCGTTA
c.817_818insTCGCCAACATCGCCCACGGCTGCAACTCCGTTACCGCCACCCGCCTCGCCCTGCATCTGGCCGATTATGCCGTTA (p.Ser273delinsPheAlaAsnIleAlaHisGlyCysAsnSerValThrAlaThrArgLeuAlaLeuHisLeuAlaAspTyrAlaValThr)
19g.18596763A>CCA404850712CRLF1c.883T>G (p.Ser295Ala)
c.348T>G
c.817T>G (p.Ser273Ala)
19g.18596763A>GCA404850713CRLF1c.883T>C (p.Ser295Pro)
c.348T>C
c.817T>C (p.Ser273Pro)
19g.18596763A>TCA404850714CRLF1c.883T>A (p.Ser295Thr)
c.348T>A
c.817T>A (p.Ser273Thr)
19g.18596764G>ACA506116418CRLF1c.882C>T (p.Thr294=)
c.347C>T
c.816C>T (p.Thr272=)
19g.18596764G>CCA9314059CRLF1c.882C>G (p.Thr294=)
c.347C>G
c.816C>G (p.Thr272=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.18596764G=CA2326432291CRLF1c.882C= (p.Thr294=)
c.347C=
c.816C= (p.Thr272=)
19g.18596764G>TCA506116417CRLF1c.882C>A (p.Thr294=)
c.347C>A
c.816C>A (p.Thr272=)
19g.18596764_18596765delCA2583602703CRLF1c.881_882del (p.Thr294IlefsTer?)
c.346_347del
c.815_816del (p.Thr272IlefsTer?)
gnomAD v4
19g.18596765G>ACA404850715CRLF1c.881C>T (p.Thr294Ile)
c.346C>T
c.815C>T (p.Thr272Ile)
dbSNP gnomAD v3 gnomAD v4
19g.18596765G>CCA404850716CRLF1c.881C>G (p.Thr294Ser)
c.346C>G
c.815C>G (p.Thr272Ser)
19g.18596765G=CA2326432292CRLF1c.881C= (p.Thr294=)
c.346C=
c.815C= (p.Thr272=)
19g.18596765G>TCA404850717CRLF1c.881C>A (p.Thr294Asn)
c.346C>A
c.815C>A (p.Thr272Asn)
19g.18596766T>ACA404850718CRLF1c.880A>T (p.Thr294Ser)
c.345A>T
c.814A>T (p.Thr272Ser)
19g.18596766T>CCA404850719CRLF1c.880A>G (p.Thr294Ala)
c.345A>G
c.814A>G (p.Thr272Ala)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.18596766T>GCA404850720CRLF1c.880A>C (p.Thr294Pro)
c.345A>C
c.814A>C (p.Thr272Pro)
19g.18596766T=CA2326432293CRLF1c.880A= (p.Thr294=)
c.345A=
c.814A= (p.Thr272=)
19g.18596767C>ACA404850721CRLF1c.879G>T (p.Gln293His)
c.344G>T
c.813G>T (p.Gln271His)
19g.18596767C>GCA404850722CRLF1c.879G>C (p.Gln293His)
c.344G>C
c.813G>C (p.Gln271His)
19g.18596767C>TCA506116419CRLF1c.879G>A (p.Gln293=)
c.344G>A
c.813G>A (p.Gln271=)
19g.18596768T>ACA404850723CRLF1c.878A>T (p.Gln293Leu)
c.343A>T
c.812A>T (p.Gln271Leu)
19g.18596768T>CCA404850724CRLF1c.878A>G (p.Gln293Arg)
c.343A>G
c.812A>G (p.Gln271Arg)
gnomAD v4
19g.18596768T>GCA404850725CRLF1c.878A>C (p.Gln293Pro)
c.343A>C
c.812A>C (p.Gln271Pro)
19g.18596769G>ACA404850726CRLF1c.877C>T (p.Gln293Ter)
c.342C>T
c.811C>T (p.Gln271Ter)
gnomAD v4
19g.18596769G>CCA404850727CRLF1c.877C>G (p.Gln293Glu)
c.342C>G
c.811C>G (p.Gln271Glu)
19g.18596769G=CA2326432294CRLF1c.877C= (p.Gln293=)
c.342C=
c.811C= (p.Gln271=)
19g.18596769G>TCA9314060CRLF1c.877C>A (p.Gln293Lys)
c.342C>A
c.811C>A (p.Gln271Lys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.18596770G>ACA506116420CRLF1c.876C>T (p.Asn292=)
c.341C>T
c.810C>T (p.Asn270=)
19g.18596770G>CCA404850729CRLF1c.876C>G (p.Asn292Lys)
c.341C>G
c.810C>G (p.Asn270Lys)
19g.18596770G>TCA404850728CRLF1c.876C>A (p.Asn292Lys)
c.341C>A
c.810C>A (p.Asn270Lys)
19g.18596771T>ACA404850730CRLF1c.875A>T (p.Asn292Ile)
c.340A>T
c.809A>T (p.Asn270Ile)
19g.18596771T>CCA404850731CRLF1c.875A>G (p.Asn292Ser)
c.340A>G
c.809A>G (p.Asn270Ser)
gnomAD v4
19g.18596771T>GCA404850732CRLF1c.875A>C (p.Asn292Thr)
c.340A>C
c.809A>C (p.Asn270Thr)
19g.18596772T>ACA404850733CRLF1c.874A>T (p.Asn292Tyr)
c.339A>T
c.808A>T (p.Asn270Tyr)
19g.18596772T>CCA404850734CRLF1c.874A>G (p.Asn292Asp)
c.339A>G
c.808A>G (p.Asn270Asp)
19g.18596772T>GCA404850735CRLF1c.874A>C (p.Asn292His)
c.339A>C
c.808A>C (p.Asn270His)
19g.18596773G>ACA306260384CRLF1c.873C>T (p.Ser291=)
c.338C>T
c.807C>T (p.Ser269=)
dbSNP gnomAD v3 gnomAD v4
19g.18596773G>CCA404850737CRLF1c.873C>G (p.Ser291Arg)
c.338C>G
c.807C>G (p.Ser269Arg)
gnomAD v4
19g.18596773G=CA2326432295CRLF1c.873C= (p.Ser291=)
c.338C=
c.807C= (p.Ser269=)
19g.18596773G>TCA404850736CRLF1c.873C>A (p.Ser291Arg)
c.338C>A
c.807C>A (p.Ser269Arg)
19g.18596774C>ACA404850738CRLF1c.872G>T (p.Ser291Ile)
c.337G>T
c.806G>T (p.Ser269Ile)
19g.18596774C=CA2326432296CRLF1c.872G= (p.Ser291=)
c.337G=
c.806G= (p.Ser269=)
19g.18596774C>GCA404850739CRLF1c.872G>C (p.Ser291Thr)
c.337G>C
c.806G>C (p.Ser269Thr)
19g.18596774C>TCA404850740CRLF1c.872G>A (p.Ser291Asn)
c.337G>A
c.806G>A (p.Ser269Asn)
dbSNP gnomAD v2 gnomAD v4
19g.18596775T>ACA404850741CRLF1c.871A>T (p.Ser291Cys)
c.336A>T
c.805A>T (p.Ser269Cys)
19g.18596775T>CCA404850742CRLF1c.871A>G (p.Ser291Gly)
c.336A>G
c.805A>G (p.Ser269Gly)
19g.18596775T>GCA404850743CRLF1c.871A>C (p.Ser291Arg)
c.336A>C
c.805A>C (p.Ser269Arg)
19g.18596776C>ACA506116423CRLF1c.870G>T (p.Val290=)
c.335G>T
c.804G>T (p.Val268=)
gnomAD v4
19g.18596776C=CA2326432297CRLF1c.870G= (p.Val290=)
c.335G=
c.804G= (p.Val268=)
19g.18596776C>GCA506116425CRLF1c.870G>C (p.Val290=)
c.335G>C
c.804G>C (p.Val268=)
19g.18596776C>TCA9314061CRLF1c.870G>A (p.Val290=)
c.335G>A
c.804G>A (p.Val268=)
dbSNP ExAC gnomAD v2
19g.18596777A>CCA404850744CRLF1c.869T>G (p.Val290Gly)
c.334T>G
c.803T>G (p.Val268Gly)
gnomAD v4
19g.18596777A>GCA404850745CRLF1c.869T>C (p.Val290Ala)
c.334T>C
c.803T>C (p.Val268Ala)
gnomAD v4
19g.18596777A>TCA404850746CRLF1c.869T>A (p.Val290Glu)
c.334T>A
c.803T>A (p.Val268Glu)
19g.18596778C>ACA404850749CRLF1c.868G>T (p.Val290Leu)
c.333G>T
c.802G>T (p.Val268Leu)
19g.18596778C>GCA404850748CRLF1c.868G>C (p.Val290Leu)
c.333G>C
c.802G>C (p.Val268Leu)
19g.18596778C>TCA404850747CRLF1c.868G>A (p.Val290Met)
c.333G>A
c.802G>A (p.Val268Met)
19g.18596779A>CCA404850750CRLF1c.867T>G (p.Asp289Glu)
c.332T>G
c.801T>G (p.Asp267Glu)
19g.18596779A>GCA506116428CRLF1c.867T>C (p.Asp289=)
c.332T>C
c.801T>C (p.Asp267=)
19g.18596779A>TCA404850751CRLF1c.867T>A (p.Asp289Glu)
c.332T>A
c.801T>A (p.Asp267Glu)
19g.18596780T>ACA9314062CRLF1c.866A>T (p.Asp289Val)
c.331A>T
c.800A>T (p.Asp267Val)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.18596780T>CCA404850752CRLF1c.866A>G (p.Asp289Gly)
c.331A>G
c.800A>G (p.Asp267Gly)
19g.18596780T>GCA404850753CRLF1c.866A>C (p.Asp289Ala)
c.331A>C
c.800A>C (p.Asp267Ala)
19g.18596780T=CA2326432298CRLF1c.866A= (p.Asp289=)
c.331A=
c.800A= (p.Asp267=)
19g.18596781C>ACA404850754CRLF1c.865G>T (p.Asp289Tyr)
c.330G>T
c.799G>T (p.Asp267Tyr)
19g.18596781C=CA2326432300CRLF1c.865G= (p.Asp289=)
c.330G=
c.799G= (p.Asp267=)
19g.18596781C>GCA404850755CRLF1c.865G>C (p.Asp289His)
c.330G>C
c.799G>C (p.Asp267His)
19g.18596781C>TCA9314063CRLF1c.865G>A (p.Asp289Asn)
c.330G>A
c.799G>A (p.Asp267Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.18596781_18596789delinsCGTCCACCACA2326432299CRLF1c.857_865delinsTGGTGGACG (p.Val286=)
c.322_330delinsTGGTGGACG
c.791_799delinsTGGTGGACG (p.Val264=)
19g.18596782G>ACA506116432CRLF1c.864C>T (p.Asp288=)
c.329C>T
c.798C>T (p.Asp266=)
dbSNP gnomAD v4
19g.18596782G>CCA404850756CRLF1c.864C>G (p.Asp288Glu)
c.329C>G
c.798C>G (p.Asp266Glu)
19g.18596782G=CA2326432301CRLF1c.864C= (p.Asp288=)
c.329C=
c.798C= (p.Asp266=)
19g.18596782G>TCA404850757CRLF1c.864C>A (p.Asp288Glu)
c.329C>A
c.798C>A (p.Asp266Glu)
19g.18596782_18596789delCA341512CRLF1c.857_864del (p.Val286GlyfsTer?)
c.322_329del
c.791_798del (p.Val264GlyfsTer?)
ClinVar dbSNP
19g.18596783T>ACA404850758CRLF1c.863A>T (p.Asp288Val)
c.328A>T
c.797A>T (p.Asp266Val)
19g.18596783T>CCA404850759CRLF1c.863A>G (p.Asp288Gly)
c.328A>G
c.797A>G (p.Asp266Gly)
19g.18596783T>GCA404850760CRLF1c.863A>C (p.Asp288Ala)
c.328A>C
c.797A>C (p.Asp266Ala)
19g.18596784C>ACA404850763CRLF1c.862G>T (p.Asp288Tyr)
c.327G>T
c.796G>T (p.Asp266Tyr)
19g.18596784C>GCA404850761CRLF1c.862G>C (p.Asp288His)
c.327G>C
c.796G>C (p.Asp266His)
19g.18596784C>TCA404850762CRLF1c.862G>A (p.Asp288Asn)
c.327G>A
c.796G>A (p.Asp266Asn)
19g.18596785C>ACA506116435CRLF1c.861G>T (p.Val287=)
c.326G>T
c.795G>T (p.Val265=)
19g.18596785C>GCA506116439CRLF1c.861G>C (p.Val287=)
c.326G>C
c.795G>C (p.Val265=)
ClinVar
19g.18596785C>TCA506116437CRLF1c.861G>A (p.Val287=)
c.326G>A
c.795G>A (p.Val265=)
19g.18596786A=CA2326432302CRLF1c.860T= (p.Val287=)
c.325T=
c.794T= (p.Val265=)
19g.18596786A>CCA404850764CRLF1c.860T>G (p.Val287Gly)
c.325T>G
c.794T>G (p.Val265Gly)
19g.18596786A>GCA404850765CRLF1c.860T>C (p.Val287Ala)
c.325T>C
c.794T>C (p.Val265Ala)
dbSNP gnomAD v3 gnomAD v4
19g.18596786A>TCA404850766CRLF1c.860T>A (p.Val287Glu)
c.325T>A
c.794T>A (p.Val265Glu)
19g.18596787C>ACA404850767CRLF1c.859G>T (p.Val287Leu)
c.324G>T
c.793G>T (p.Val265Leu)
19g.18596787C>GCA404850768CRLF1c.859G>C (p.Val287Leu)
c.324G>C
c.793G>C (p.Val265Leu)
19g.18596787C>TCA404850769CRLF1c.859G>A (p.Val287Met)
c.324G>A
c.793G>A (p.Val265Met)
19g.18596788C>ACA506116444CRLF1c.858G>T (p.Val286=)
c.323G>T
c.792G>T (p.Val264=)
19g.18596788C>GCA506116446CRLF1c.858G>C (p.Val286=)
c.323G>C
c.792G>C (p.Val264=)
19g.18596788C>TCA506116447CRLF1c.858G>A (p.Val286=)
c.323G>A
c.792G>A (p.Val264=)
19g.18596789A>CCA404850770CRLF1c.857T>G (p.Val286Gly)
c.322T>G
c.791T>G (p.Val264Gly)
19g.18596789A>GCA404850771CRLF1c.857T>C (p.Val286Ala)
c.322T>C
c.791T>C (p.Val264Ala)
19g.18596789A>TCA404850772CRLF1c.857T>A (p.Val286Glu)
c.322T>A
c.791T>A (p.Val264Glu)
gnomAD v4
19g.18596789_18596790insAACACACCA2813827705CRLF1c.856_857insGTGTGTT (p.Val286GlyfsTer?)
c.321_322insGTGTGTT
c.790_791insGTGTGTT (p.Val264GlyfsTer?)
19g.18596790C>ACA404850773CRLF1c.856G>T (p.Val286Leu)
c.321G>T
c.790G>T (p.Val264Leu)
19g.18596790C=CA2326432303CRLF1c.856G= (p.Val286=)
c.321G=
c.790G= (p.Val264=)
19g.18596790C>GCA404850774CRLF1c.856G>C (p.Val286Leu)
c.321G>C
c.790G>C (p.Val264Leu)
19g.18596790C>TCA9314064CRLF1c.856G>A (p.Val286Met)
c.321G>A
c.790G>A (p.Val264Met)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.18596791C>ACA404850777CRLF1c.856-1G>T (n.856-1G>T)
c.321-1G>T
c.790-1G>T (n.790-1G>T)
19g.18596791C>GCA404850776CRLF1c.856-1G>C (n.856-1G>C)
c.321-1G>C
c.790-1G>C (n.790-1G>C)
19g.18596791C>TCA404850775CRLF1c.856-1G>A (n.856-1G>A)
c.321-1G>A
c.790-1G>A (n.790-1G>A)
19g.18596792T>ACA404850780CRLF1c.856-2A>T (n.856-2A>T)
c.321-2A>T
c.790-2A>T (n.790-2A>T)
19g.18596792T>CCA404850778CRLF1c.856-2A>G (n.856-2A>G)
c.321-2A>G
c.790-2A>G (n.790-2A>G)
19g.18596792T>GCA404850779CRLF1c.856-2A>C (n.856-2A>C)
c.321-2A>C
c.790-2A>C (n.790-2A>C)
COSMIC
19g.18596793G>ACA2813827708CRLF1c.856-3C>T (n.856-3C>T)
c.321-3C>T
c.790-3C>T (n.790-3C>T)
19g.18596794G>CCA2813827709CRLF1c.856-4C>G (n.856-4C>G)
c.321-4C>G
c.790-4C>G (n.790-4C>G)
19g.18596795A=CA2326432304CRLF1c.856-5T= (n.856-5T=)
c.321-5T=
c.790-5T= (n.790-5T=)
19g.18596795A>TCA632626056CRLF1c.856-5T>A (n.856-5T>A)
c.321-5T>A
c.790-5T>A (n.790-5T>A)
dbSNP gnomAD v2 gnomAD v4
19g.18596796C=CA2326432305CRLF1c.856-6G= (n.856-6G=)
c.321-6G=
c.790-6G= (n.790-6G=)
19g.18596796C>GCA783933610CRLF1c.856-6G>C (n.856-6G>C)
c.321-6G>C
c.790-6G>C (n.790-6G>C)
dbSNP gnomAD v3 gnomAD v4
19g.18596796C>TCA306260394CRLF1c.856-6G>A (n.856-6G>A)
c.321-6G>A
c.790-6G>A (n.790-6G>A)
dbSNP gnomAD v2 gnomAD v4
19g.18596799T>CCA2583602722CRLF1c.856-9A>G (n.856-9A>G)
c.321-9A>G
c.790-9A>G (n.790-9A>G)
gnomAD v4
19g.18596801A>CCA2583602723CRLF1c.856-11T>G (n.856-11T>G)
c.321-11T>G
c.790-11T>G (n.790-11T>G)
gnomAD v4
19g.18596802G>ACA2583602724CRLF1c.856-12C>T (n.856-12C>T)
c.321-12C>T
c.790-12C>T (n.790-12C>T)
gnomAD v4
19g.18596802G>CCA632626057CRLF1c.856-12C>G (n.856-12C>G)
c.321-12C>G
c.790-12C>G (n.790-12C>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.18596802G=CA2326432306CRLF1c.856-12C= (n.856-12C=)
c.321-12C=
c.790-12C= (n.790-12C=)
19g.18596803G>ACA2576724683CRLF1c.856-13C>T (n.856-13C>T)
c.321-13C>T
c.790-13C>T (n.790-13C>T)
gnomAD v4
19g.18596805C=CA2326432307CRLF1c.856-15G= (n.856-15G=)
c.321-15G=
c.790-15G= (n.790-15G=)
19g.18596805C>GCA632626058CRLF1c.856-15G>C (n.856-15G>C)
c.321-15G>C
c.790-15G>C (n.790-15G>C)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.18596806A=CA2326432308CRLF1c.856-16T= (n.856-16T=)
c.321-16T=
c.790-16T= (n.790-16T=)
19g.18596806A>GCA306260413CRLF1c.856-16T>C (n.856-16T>C)
c.321-16T>C
c.790-16T>C (n.790-16T>C)
dbSNP gnomAD v2 gnomAD v4
19g.18596806A>TCA2583602726CRLF1c.856-16T>A (n.856-16T>A)
c.321-16T>A
c.790-16T>A (n.790-16T>A)
gnomAD v4
19g.18596807A>GCA2576724684CRLF1c.856-17T>C (n.856-17T>C)
c.321-17T>C
c.790-17T>C (n.790-17T>C)
19g.18596807_18596808delinsAGCA2326432309CRLF1c.856-18_856-17delinsCT (n.856-18_856-17delinsCT)
c.321-18_321-17delinsCT
c.790-18_790-17delinsCT (n.790-18_790-17delinsCT)
19g.18596808G>ACA2326432312CRLF1c.856-18C>T (n.856-18C>T)
c.321-18C>T
c.790-18C>T (n.790-18C>T)
dbSNP gnomAD v4
19g.18596808G=CA2326432310CRLF1c.856-18C= (n.856-18C=)
c.321-18C=
c.790-18C= (n.790-18C=)
19g.18596808G>TCA2583602727CRLF1c.856-18C>A (n.856-18C>A)
c.321-18C>A
c.790-18C>A (n.790-18C>A)
gnomAD v4
19g.18596809delCA2326432311CRLF1c.856-18del (n.856-18del)
c.321-18del
c.790-18del (n.790-18del)
dbSNP gnomAD v4
19g.18596810T>CCA306260417CRLF1c.856-20A>G (n.856-20A>G)
c.321-20A>G
c.790-20A>G (n.790-20A>G)
dbSNP
19g.18596810T=CA2326432313CRLF1c.856-20A= (n.856-20A=)
c.321-20A=
c.790-20A= (n.790-20A=)
19g.18596811C>ACA2813827711CRLF1c.856-21G>T (n.856-21G>T)
c.321-21G>T
c.790-21G>T (n.790-21G>T)
19g.18596811C=CA2326432315CRLF1c.856-21G= (n.856-21G=)
c.321-21G=
c.790-21G= (n.790-21G=)
19g.18596811C>TCA632626059CRLF1c.856-21G>A (n.856-21G>A)
c.321-21G>A
c.790-21G>A (n.790-21G>A)
dbSNP gnomAD v2 gnomAD v4
19g.18596811_18596816delinsCAGAGTCA2326432314CRLF1c.856-26_856-21delinsACTCTG (n.856-26_856-21delinsACTCTG)
c.321-26_321-21delinsACTCTG
c.790-26_790-21delinsACTCTG (n.790-26_790-21delinsACTCTG)
19g.18596812A=CA2326432316CRLF1c.856-22T= (n.856-22T=)
c.321-22T=
c.790-22T= (n.790-22T=)
19g.18596812A>CCA9314066CRLF1c.856-22T>G (n.856-22T>G)
c.321-22T>G
c.790-22T>G (n.790-22T>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.18596812A>GCA632626060CRLF1c.856-22T>C (n.856-22T>C)
c.321-22T>C
c.790-22T>C (n.790-22T>C)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.18596814_18596815delCA2583602728CRLF1c.856-23_856-22del (n.856-23_856-22del)
c.321-23_321-22del
c.790-23_790-22del (n.790-23_790-22del)
gnomAD v4
19g.18596816_18596820delCA9314065CRLF1c.856-26_856-22del (n.856-26_856-22del)
c.321-26_321-22del
c.790-26_790-22del (n.790-26_790-22del)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.18596813G>CCA2583602730CRLF1c.856-23C>G (n.856-23C>G)
c.321-23C>G
c.790-23C>G (n.790-23C>G)
gnomAD v4
19g.18596813G>TCA2583602731CRLF1c.856-23C>A (n.856-23C>A)
c.321-23C>A
c.790-23C>A (n.790-23C>A)
gnomAD v4
19g.18596814A=CA2326432317CRLF1c.856-24T= (n.856-24T=)
c.321-24T=
c.790-24T= (n.790-24T=)
19g.18596814A>CCA2583602733CRLF1c.856-24T>G (n.856-24T>G)
c.321-24T>G
c.790-24T>G (n.790-24T>G)
gnomAD v4
19g.18596814A>GCA9314067CRLF1c.856-24T>C (n.856-24T>C)
c.321-24T>C
c.790-24T>C (n.790-24T>C)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.18596815G>ACA632626061CRLF1c.856-25C>T (n.856-25C>T)
c.321-25C>T
c.790-25C>T (n.790-25C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.18596815G=CA2326432318CRLF1c.856-25C= (n.856-25C=)
c.321-25C=
c.790-25C= (n.790-25C=)
19g.18596816T>CCA2576724685CRLF1c.856-26A>G (n.856-26A>G)
c.321-26A>G
c.790-26A>G (n.790-26A>G)
19g.18596817A=CA2326432319CRLF1c.856-27T= (n.856-27T=)
c.321-27T=
c.790-27T= (n.790-27T=)

Number of alleles fetched