Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.174571912G>ACA1974037WIPF1c.893C>T (p.Pro298Leu)
n.898C>T
c.515C>T (p.Pro172Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.174571912G>CCA1974038WIPF1c.893C>G (p.Pro298Arg)
n.898C>G
c.515C>G (p.Pro172Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.174571912G=CA1308757352WIPF1c.893C= (p.Pro298=)
n.898C=
c.515C= (p.Pro172=)
2g.174571912G>TCA349341291WIPF1c.893C>A (p.Pro298Gln)
n.898C>A
c.515C>A (p.Pro172Gln)
2g.174571913G>ACA349341297WIPF1c.892C>T (p.Pro298Ser)
n.897C>T
c.514C>T (p.Pro172Ser)
gnomAD v4
2g.174571913G>CCA349341294WIPF1c.892C>G (p.Pro298Ala)
n.897C>G
c.514C>G (p.Pro172Ala)
2g.174571913G>TCA349341293WIPF1c.892C>A (p.Pro298Thr)
n.897C>A
c.514C>A (p.Pro172Thr)
2g.174571914A=CA1308757353WIPF1c.891T= (p.Thr297=)
n.896T=
c.513T= (p.Thr171=)
2g.174571914A>CCA430228618WIPF1c.891T>G (p.Thr297=)
n.896T>G
c.513T>G (p.Thr171=)
2g.174571914A>GCA430228617WIPF1c.891T>C (p.Thr297=)
n.896T>C
c.513T>C (p.Thr171=)
dbSNP
2g.174571914A>TCA430228615WIPF1c.891T>A (p.Thr297=)
n.896T>A
c.513T>A (p.Thr171=)
2g.174571915G>ACA349341299WIPF1c.890C>T (p.Thr297Ile)
n.895C>T
c.512C>T (p.Thr171Ile)
gnomAD v4
2g.174571915G>CCA349341301WIPF1c.890C>G (p.Thr297Ser)
n.895C>G
c.512C>G (p.Thr171Ser)
gnomAD v4
2g.174571915G>TCA349341303WIPF1c.890C>A (p.Thr297Asn)
n.895C>A
c.512C>A (p.Thr171Asn)
2g.174571916T>ACA1974039WIPF1c.889A>T (p.Thr297Ser)
n.894A>T
c.511A>T (p.Thr171Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.174571916T>CCA349341306WIPF1c.889A>G (p.Thr297Ala)
n.894A>G
c.511A>G (p.Thr171Ala)
COSMIC COSMIC COSMIC
2g.174571916T>GCA349341308WIPF1c.889A>C (p.Thr297Pro)
n.894A>C
c.511A>C (p.Thr171Pro)
2g.174571916T=CA1308757354WIPF1c.889A= (p.Thr297=)
n.894A=
c.511A= (p.Thr171=)
2g.174571917G>ACA430228620WIPF1c.888C>T (p.Ser296=)
n.893C>T
c.510C>T (p.Ser170=)
gnomAD v4
2g.174571917G>CCA430228621WIPF1c.888C>G (p.Ser296=)
n.893C>G
c.510C>G (p.Ser170=)
2g.174571917G>TCA430228622WIPF1c.888C>A (p.Ser296=)
n.893C>A
c.510C>A (p.Ser170=)
2g.174571918G>ACA349341310WIPF1c.887C>T (p.Ser296Phe)
n.892C>T
c.509C>T (p.Ser170Phe)
2g.174571918G>CCA349341312WIPF1c.887C>G (p.Ser296Cys)
n.892C>G
c.509C>G (p.Ser170Cys)
2g.174571918G=CA1308757355WIPF1c.887C= (p.Ser296=)
n.892C=
c.509C= (p.Ser170=)
2g.174571918G>TCA1974040WIPF1c.887C>A (p.Ser296Tyr)
n.892C>A
c.509C>A (p.Ser170Tyr)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.174571919A>CCA349341315WIPF1c.886T>G (p.Ser296Ala)
n.891T>G
c.508T>G (p.Ser170Ala)
2g.174571919A>GCA349341317WIPF1c.886T>C (p.Ser296Pro)
n.891T>C
c.508T>C (p.Ser170Pro)
2g.174571919A>TCA349341318WIPF1c.886T>A (p.Ser296Thr)
n.891T>A
c.508T>A (p.Ser170Thr)
2g.174571920A=CA1308757356WIPF1c.885T= (p.Pro295=)
n.890T=
c.507T= (p.Pro169=)
2g.174571920A>CCA430228626WIPF1c.885T>G (p.Pro295=)
n.890T>G
c.507T>G (p.Pro169=)
2g.174571920A>GCA60843245WIPF1c.885T>C (p.Pro295=)
n.890T>C
c.507T>C (p.Pro169=)
dbSNP
2g.174571920A>TCA430228627WIPF1c.885T>A (p.Pro295=)
n.890T>A
c.507T>A (p.Pro169=)
2g.174571921G>ACA349341325WIPF1c.884C>T (p.Pro295Leu)
n.889C>T
c.506C>T (p.Pro169Leu)
gnomAD v4
2g.174571921G>CCA349341321WIPF1c.884C>G (p.Pro295Arg)
n.889C>G
c.506C>G (p.Pro169Arg)
2g.174571921G>TCA349341323WIPF1c.884C>A (p.Pro295His)
n.889C>A
c.506C>A (p.Pro169His)
2g.174571922delCA2662015762WIPF1c.884del (p.Pro295LeufsTer?)
n.889del
c.506del (p.Pro169LeufsTer?)
gnomAD v4
2g.174571922G>ACA349341327WIPF1c.883C>T (p.Pro295Ser)
n.888C>T
c.505C>T (p.Pro169Ser)
2g.174571922G>CCA349341329WIPF1c.883C>G (p.Pro295Ala)
n.888C>G
c.505C>G (p.Pro169Ala)
2g.174571922G>TCA349341331WIPF1c.883C>A (p.Pro295Thr)
n.888C>A
c.505C>A (p.Pro169Thr)
2g.174571923C>ACA430228628WIPF1c.882G>T (p.Val294=)
n.887G>T
c.504G>T (p.Val168=)
dbSNP gnomAD v3 gnomAD v4
2g.174571923C=CA1308757357WIPF1c.882G= (p.Val294=)
n.887G=
c.504G= (p.Val168=)
2g.174571923C>GCA430228629WIPF1c.882G>C (p.Val294=)
n.887G>C
c.504G>C (p.Val168=)
2g.174571923C>TCA430228631WIPF1c.882G>A (p.Val294=)
n.887G>A
c.504G>A (p.Val168=)
2g.174571924A>CCA349341334WIPF1c.881T>G (p.Val294Gly)
n.886T>G
c.503T>G (p.Val168Gly)
2g.174571924A>GCA349341335WIPF1c.881T>C (p.Val294Ala)
n.886T>C
c.503T>C (p.Val168Ala)
2g.174571924A>TCA349341337WIPF1c.881T>A (p.Val294Glu)
n.886T>A
c.503T>A (p.Val168Glu)
2g.174571925C>ACA349341339WIPF1c.880G>T (p.Val294Leu)
n.885G>T
c.502G>T (p.Val168Leu)
2g.174571925C=CA1308757358WIPF1c.880G= (p.Val294=)
n.885G=
c.502G= (p.Val168=)
2g.174571925C>GCA349341341WIPF1c.880G>C (p.Val294Leu)
n.885G>C
c.502G>C (p.Val168Leu)
dbSNP
2g.174571925C>TCA60843247WIPF1c.880G>A (p.Val294Met)
n.885G>A
c.502G>A (p.Val168Met)
dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC
2g.174571926T>ACA430228634WIPF1c.879A>T (p.Pro293=)
n.884A>T
c.501A>T (p.Pro167=)
2g.174571926T>CCA430228635WIPF1c.879A>G (p.Pro293=)
n.884A>G
c.501A>G (p.Pro167=)
2g.174571926T>GCA430228636WIPF1c.879A>C (p.Pro293=)
n.884A>C
c.501A>C (p.Pro167=)
2g.174571927G>ACA349341343WIPF1c.878C>T (p.Pro293Leu)
n.883C>T
c.500C>T (p.Pro167Leu)
COSMIC COSMIC COSMIC
2g.174571927G>CCA349341345WIPF1c.878C>G (p.Pro293Arg)
n.883C>G
c.500C>G (p.Pro167Arg)
2g.174571927G>TCA349341347WIPF1c.878C>A (p.Pro293Gln)
n.883C>A
c.500C>A (p.Pro167Gln)
2g.174571928G>ACA349341353WIPF1c.877C>T (p.Pro293Ser)
n.882C>T
c.499C>T (p.Pro167Ser)
2g.174571928G>CCA349341351WIPF1c.877C>G (p.Pro293Ala)
n.882C>G
c.499C>G (p.Pro167Ala)
2g.174571928G>TCA349341349WIPF1c.877C>A (p.Pro293Thr)
n.882C>A
c.499C>A (p.Pro167Thr)
2g.174571929A=CA1308757359WIPF1c.876T= (p.Pro292=)
n.881T=
c.498T= (p.Pro166=)
2g.174571929A>CCA430228641WIPF1c.876T>G (p.Pro292=)
n.881T>G
c.498T>G (p.Pro166=)
2g.174571929A>GCA430228642WIPF1c.876T>C (p.Pro292=)
n.881T>C
c.498T>C (p.Pro166=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.174571929A>TCA430228640WIPF1c.876T>A (p.Pro292=)
n.881T>A
c.498T>A (p.Pro166=)
2g.174571930G>ACA349341358WIPF1c.875C>T (p.Pro292Leu)
n.880C>T
c.497C>T (p.Pro166Leu)
gnomAD v4
2g.174571930G>CCA349341356WIPF1c.875C>G (p.Pro292Arg)
n.880C>G
c.497C>G (p.Pro166Arg)
2g.174571930G>TCA349341360WIPF1c.875C>A (p.Pro292His)
n.880C>A
c.497C>A (p.Pro166His)
COSMIC COSMIC
2g.174571931G>ACA1974041WIPF1c.874C>T (p.Pro292Ser)
n.879C>T
c.496C>T (p.Pro166Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.174571931G>CCA349341362WIPF1c.874C>G (p.Pro292Ala)
n.879C>G
c.496C>G (p.Pro166Ala)
gnomAD v4
2g.174571931G=CA1308757360WIPF1c.874C= (p.Pro292=)
n.879C=
c.496C= (p.Pro166=)
2g.174571931G>TCA349341363WIPF1c.874C>A (p.Pro292Thr)
n.879C>A
c.496C>A (p.Pro166Thr)
gnomAD v4
2g.174571932C>ACA349341364WIPF1c.873G>T (p.Lys291Asn)
n.878G>T
c.495G>T (p.Lys165Asn)
gnomAD v4
2g.174571932C=CA1308757361WIPF1c.873G= (p.Lys291=)
n.878G=
c.495G= (p.Lys165=)
2g.174571932C>GCA349341365WIPF1c.873G>C (p.Lys291Asn)
n.878G>C
c.495G>C (p.Lys165Asn)
2g.174571932C>TCA1974043WIPF1c.873G>A (p.Lys291=)
n.878G>A
c.495G>A (p.Lys165=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.174571932_174571935delinsCTTGCA1308757362WIPF1c.870_873delinsCAAG (p.Asn290=)
n.875_878delinsCAAG
c.492_495delinsCAAG (p.Asn164=)
2g.174571933T>ACA349341366WIPF1c.872A>T (p.Lys291Met)
n.877A>T
c.494A>T (p.Lys165Met)
2g.174571933T>CCA349341367WIPF1c.872A>G (p.Lys291Arg)
n.877A>G
c.494A>G (p.Lys165Arg)
2g.174571933T>GCA349341368WIPF1c.872A>C (p.Lys291Thr)
n.877A>C
c.494A>C (p.Lys165Thr)
dbSNP
2g.174571933T=CA1308757363WIPF1c.872A= (p.Lys291=)
n.877A=
c.494A= (p.Lys165=)
2g.174571938_174571940delCA1974042WIPF1c.870_872del (p.Asn290del)
n.875_877del
c.492_494del (p.Asn164del)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.174571934T>ACA349341369WIPF1c.871A>T (p.Lys291Ter)
n.876A>T
c.493A>T (p.Lys165Ter)
2g.174571934T>CCA349341370WIPF1c.871A>G (p.Lys291Glu)
n.876A>G
c.493A>G (p.Lys165Glu)
dbSNP
2g.174571934T>GCA349341371WIPF1c.871A>C (p.Lys291Gln)
n.876A>C
c.493A>C (p.Lys165Gln)
2g.174571934_174571935delinsTGCA1308757364WIPF1c.870_871delinsCA (p.Asn290=)
n.875_876delinsCA
c.492_493delinsCA (p.Asn164=)
2g.174571935delCA1974044WIPF1c.870del (p.Asn290LysfsTer?)
n.875del
c.492del (p.Asn164LysfsTer?)
dbSNP ExAC gnomAD v2
2g.174571935G>ACA430228649WIPF1c.870C>T (p.Asn290=)
n.875C>T
c.492C>T (p.Asn164=)
2g.174571935G>CCA349341375WIPF1c.870C>G (p.Asn290Lys)
n.875C>G
c.492C>G (p.Asn164Lys)
ClinVar dbSNP gnomAD v4
2g.174571935G>TCA349341373WIPF1c.870C>A (p.Asn290Lys)
n.875C>A
c.492C>A (p.Asn164Lys)
2g.174571936T>ACA349341377WIPF1c.869A>T (p.Asn290Ile)
n.874A>T
c.491A>T (p.Asn164Ile)
2g.174571936T>CCA349341378WIPF1c.869A>G (p.Asn290Ser)
n.874A>G
c.491A>G (p.Asn164Ser)
dbSNP
2g.174571936T>GCA349341381WIPF1c.869A>C (p.Asn290Thr)
n.874A>C
c.491A>C (p.Asn164Thr)
2g.174571936T=CA1308757365WIPF1c.869A= (p.Asn290=)
n.874A=
c.491A= (p.Asn164=)
2g.174571937T>ACA349341385WIPF1c.868A>T (p.Asn290Tyr)
n.873A>T
c.490A>T (p.Asn164Tyr)
2g.174571937T>CCA349341387WIPF1c.868A>G (p.Asn290Asp)
n.873A>G
c.490A>G (p.Asn164Asp)
gnomAD v4
2g.174571937T>GCA349341389WIPF1c.868A>C (p.Asn290His)
n.873A>C
c.490A>C (p.Asn164His)
2g.174571938G>ACA430228650WIPF1c.867C>T (p.Asn289=)
n.872C>T
c.489C>T (p.Asn163=)
dbSNP
2g.174571938G>CCA349341391WIPF1c.867C>G (p.Asn289Lys)
n.872C>G
c.489C>G (p.Asn163Lys)
2g.174571938G>TCA349341393WIPF1c.867C>A (p.Asn289Lys)
n.872C>A
c.489C>A (p.Asn163Lys)
2g.174571939T>ACA349341397WIPF1c.866A>T (p.Asn289Ile)
n.871A>T
c.488A>T (p.Asn163Ile)
2g.174571939T>CCA349341398WIPF1c.866A>G (p.Asn289Ser)
n.871A>G
c.488A>G (p.Asn163Ser)
COSMIC COSMIC COSMIC
2g.174571939T>GCA349341400WIPF1c.866A>C (p.Asn289Thr)
n.871A>C
c.488A>C (p.Asn163Thr)
2g.174571940T>ACA349341405WIPF1c.865A>T (p.Asn289Tyr)
n.870A>T
c.487A>T (p.Asn163Tyr)
2g.174571940T>CCA349341403WIPF1c.865A>G (p.Asn289Asp)
n.870A>G
c.487A>G (p.Asn163Asp)
2g.174571940T>GCA349341401WIPF1c.865A>C (p.Asn289His)
n.870A>C
c.487A>C (p.Asn163His)
2g.174571941C>ACA349341406WIPF1c.864G>T (p.Gln288His)
n.869G>T
c.486G>T (p.Gln162His)
gnomAD v4
2g.174571941C=CA1308757366WIPF1c.864G= (p.Gln288=)
n.869G=
c.486G= (p.Gln162=)
2g.174571941C>GCA349341408WIPF1c.864G>C (p.Gln288His)
n.869G>C
c.486G>C (p.Gln162His)
2g.174571941C>TCA60843269WIPF1c.864G>A (p.Gln288=)
n.869G>A
c.486G>A (p.Gln162=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.174571942T>ACA349341410WIPF1c.863A>T (p.Gln288Leu)
n.868A>T
c.485A>T (p.Gln162Leu)
2g.174571942T>CCA349341412WIPF1c.863A>G (p.Gln288Arg)
n.868A>G
c.485A>G (p.Gln162Arg)
2g.174571942T>GCA349341414WIPF1c.863A>C (p.Gln288Pro)
n.868A>C
c.485A>C (p.Gln162Pro)
2g.174571942_174571948delinsTGAGGAGCA1308757367WIPF1c.857_863delinsCTCCTCA (p.Pro286=)
n.862_868delinsCTCCTCA
c.479_485delinsCTCCTCA (p.Pro160=)
2g.174571943G>ACA349341417WIPF1c.862C>T (p.Gln288Ter)
n.867C>T
c.484C>T (p.Gln162Ter)
2g.174571943G>CCA349341419WIPF1c.862C>G (p.Gln288Glu)
n.867C>G
c.484C>G (p.Gln162Glu)
2g.174571943G>TCA349341420WIPF1c.862C>A (p.Gln288Lys)
n.867C>A
c.484C>A (p.Gln162Lys)
2g.174571953_174571955dupCA1974045WIPF1c.860_862dup (p.Pro287_Gln288insPro)
n.865_867dup
c.482_484dup (p.Pro161_Gln162insPro)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.174571950_174571955dupCA2662015791WIPF1c.857_862dup (p.Pro287_Gln288insProPro)
n.862_867dup
c.479_484dup (p.Pro161_Gln162insProPro)
gnomAD v4
2g.174571953_174571955delCA1974046WIPF1c.860_862del (p.Pro287del)
n.865_867del
c.482_484del (p.Pro161del)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
2g.174571950_174571955delCA1039437959WIPF1c.857_862del (p.Pro286_Pro287del)
n.862_867del
c.479_484del (p.Pro160_Pro161del)
dbSNP gnomAD v3 gnomAD v4
2g.174571944A=CA1308757368WIPF1c.861T= (p.Pro287=)
n.866T=
c.483T= (p.Pro161=)
2g.174571944A>CCA430228659WIPF1c.861T>G (p.Pro287=)
n.866T>G
c.483T>G (p.Pro161=)
2g.174571944A>GCA430228657WIPF1c.861T>C (p.Pro287=)
n.866T>C
c.483T>C (p.Pro161=)
dbSNP gnomAD v4
2g.174571944A>TCA430228658WIPF1c.861T>A (p.Pro287=)
n.866T>A
c.483T>A (p.Pro161=)
2g.174571945G>ACA60843275WIPF1c.860C>T (p.Pro287Leu)
n.865C>T
c.482C>T (p.Pro161Leu)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.174571945G>CCA349341424WIPF1c.860C>G (p.Pro287Arg)
n.865C>G
c.482C>G (p.Pro161Arg)
2g.174571945G=CA1308757369WIPF1c.860C= (p.Pro287=)
n.865C=
c.482C= (p.Pro161=)
2g.174571945G>TCA349341426WIPF1c.860C>A (p.Pro287His)
n.865C>A
c.482C>A (p.Pro161His)
2g.174571946G>ACA1974047WIPF1c.859C>T (p.Pro287Ser)
n.864C>T
c.481C>T (p.Pro161Ser)
dbSNP ExAC gnomAD v2
2g.174571946G>CCA349341428WIPF1c.859C>G (p.Pro287Ala)
n.864C>G
c.481C>G (p.Pro161Ala)
2g.174571946G=CA1308757370WIPF1c.859C= (p.Pro287=)
n.864C=
c.481C= (p.Pro161=)
2g.174571946G>TCA349341430WIPF1c.859C>A (p.Pro287Thr)
n.864C>A
c.481C>A (p.Pro161Thr)
gnomAD v4
2g.174571947A=CA1308757371WIPF1c.858T= (p.Pro286=)
n.863T=
c.480T= (p.Pro160=)
2g.174571947A>CCA430228662WIPF1c.858T>G (p.Pro286=)
n.863T>G
c.480T>G (p.Pro160=)
gnomAD v4
2g.174571947A>GCA430228663WIPF1c.858T>C (p.Pro286=)
n.863T>C
c.480T>C (p.Pro160=)
dbSNP gnomAD v4
2g.174571947A>TCA430228665WIPF1c.858T>A (p.Pro286=)
n.863T>A
c.480T>A (p.Pro160=)
2g.174571948G>ACA1974048WIPF1c.857C>T (p.Pro286Leu)
n.862C>T
c.479C>T (p.Pro160Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.174571948G>CCA349341434WIPF1c.857C>G (p.Pro286Arg)
n.862C>G
c.479C>G (p.Pro160Arg)
2g.174571948G=CA1308757372WIPF1c.857C= (p.Pro286=)
n.862C=
c.479C= (p.Pro160=)
2g.174571948G>TCA349341436WIPF1c.857C>A (p.Pro286His)
n.862C>A
c.479C>A (p.Pro160His)
2g.174571949G>ACA349341439WIPF1c.856C>T (p.Pro286Ser)
n.861C>T
c.478C>T (p.Pro160Ser)
2g.174571949G>CCA349341440WIPF1c.856C>G (p.Pro286Ala)
n.861C>G
c.478C>G (p.Pro160Ala)
2g.174571949G>TCA349341442WIPF1c.856C>A (p.Pro286Thr)
n.861C>A
c.478C>A (p.Pro160Thr)
2g.174571950A>CCA430228666WIPF1c.855T>G (p.Pro285=)
n.860T>G
c.477T>G (p.Pro159=)
2g.174571950A>GCA430228667WIPF1c.855T>C (p.Pro285=)
n.860T>C
c.477T>C (p.Pro159=)
2g.174571950A>TCA430228668WIPF1c.855T>A (p.Pro285=)
n.860T>A
c.477T>A (p.Pro159=)
2g.174571951G>ACA349341445WIPF1c.854C>T (p.Pro285Leu)
n.859C>T
c.476C>T (p.Pro159Leu)
2g.174571951G>CCA349341447WIPF1c.854C>G (p.Pro285Arg)
n.859C>G
c.476C>G (p.Pro159Arg)
gnomAD v4
2g.174571951G>TCA349341449WIPF1c.854C>A (p.Pro285His)
n.859C>A
c.476C>A (p.Pro159His)
2g.174571952G>ACA349341451WIPF1c.853C>T (p.Pro285Ser)
n.858C>T
c.475C>T (p.Pro159Ser)
2g.174571952G>CCA349341453WIPF1c.853C>G (p.Pro285Ala)
n.858C>G
c.475C>G (p.Pro159Ala)
2g.174571952G>TCA349341455WIPF1c.853C>A (p.Pro285Thr)
n.858C>A
c.475C>A (p.Pro159Thr)
2g.174571953A=CA1308757373WIPF1c.852T= (p.Pro284=)
n.857T=
c.474T= (p.Pro158=)
2g.174571953A>CCA430228674WIPF1c.852T>G (p.Pro284=)
n.857T>G
c.474T>G (p.Pro158=)
2g.174571953A>GCA430228672WIPF1c.852T>C (p.Pro284=)
n.857T>C
c.474T>C (p.Pro158=)
gnomAD v2 gnomAD v4
2g.174571953A>TCA430228673WIPF1c.852T>A (p.Pro284=)
n.857T>A
c.474T>A (p.Pro158=)
2g.174571954G>ACA349341458WIPF1c.851C>T (p.Pro284Leu)
n.856C>T
c.473C>T (p.Pro158Leu)
2g.174571954G>CCA349341461WIPF1c.851C>G (p.Pro284Arg)
n.856C>G
c.473C>G (p.Pro158Arg)
2g.174571954G>TCA349341457WIPF1c.851C>A (p.Pro284His)
n.856C>A
c.473C>A (p.Pro158His)
2g.174571958dupCA2753239484WIPF1c.851dup (p.Pro285SerfsTer?)
n.856dup
c.473dup (p.Pro159SerfsTer?)
2g.174571956_174571958dupCA537975060WIPF1c.849_851dup (p.Pro284_Pro285insPro)
n.854_856dup
c.471_473dup (p.Pro158_Pro159insPro)
dbSNP gnomAD v2 gnomAD v4
2g.174571955G>ACA349341463WIPF1c.850C>T (p.Pro284Ser)
n.855C>T
c.472C>T (p.Pro158Ser)
dbSNP gnomAD v4
2g.174571955G>CCA349341465WIPF1c.850C>G (p.Pro284Ala)
n.855C>G
c.472C>G (p.Pro158Ala)
2g.174571955G=CA1308757374WIPF1c.850C= (p.Pro284=)
n.855C=
c.472C= (p.Pro158=)
2g.174571955G>TCA349341464WIPF1c.850C>A (p.Pro284Thr)
n.855C>A
c.472C>A (p.Pro158Thr)
2g.174571956G>ACA430228677WIPF1c.849C>T (p.Pro283=)
n.854C>T
c.471C>T (p.Pro157=)
dbSNP gnomAD v4 COSMIC COSMIC COSMIC
2g.174571956G>CCA430228678WIPF1c.849C>G (p.Pro283=)
n.854C>G
c.471C>G (p.Pro157=)
2g.174571956G=CA1308757375WIPF1c.849C= (p.Pro283=)
n.854C=
c.471C= (p.Pro157=)
2g.174571956G>TCA430228680WIPF1c.849C>A (p.Pro283=)
n.854C>A
c.471C>A (p.Pro157=)
dbSNP
2g.174571957G>ACA1974049WIPF1c.848C>T (p.Pro283Leu)
n.853C>T
c.470C>T (p.Pro157Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.174571957G>CCA1974050WIPF1c.848C>G (p.Pro283Arg)
n.853C>G
c.470C>G (p.Pro157Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.174571957G=CA1308757376WIPF1c.848C= (p.Pro283=)
n.853C=
c.470C= (p.Pro157=)
2g.174571957G>TCA349341467WIPF1c.848C>A (p.Pro283His)
n.853C>A
c.470C>A (p.Pro157His)
2g.174571958G>ACA349341469WIPF1c.847C>T (p.Pro283Ser)
n.852C>T
c.469C>T (p.Pro157Ser)
gnomAD v4
2g.174571958G>CCA349341471WIPF1c.847C>G (p.Pro283Ala)
n.852C>G
c.469C>G (p.Pro157Ala)
2g.174571958G>TCA349341473WIPF1c.847C>A (p.Pro283Thr)
n.852C>A
c.469C>A (p.Pro157Thr)
2g.174571959A>CCA430228681WIPF1c.846T>G (p.Val282=)
n.851T>G
c.468T>G (p.Val156=)
2g.174571959A>GCA430228682WIPF1c.846T>C (p.Val282=)
n.851T>C
c.468T>C (p.Val156=)
2g.174571959A>TCA430228683WIPF1c.846T>A (p.Val282=)
n.851T>A
c.468T>A (p.Val156=)
gnomAD v4
2g.174571960A>CCA349341475WIPF1c.845T>G (p.Val282Gly)
n.850T>G
c.467T>G (p.Val156Gly)
2g.174571960A>GCA349341477WIPF1c.845T>C (p.Val282Ala)
n.850T>C
c.467T>C (p.Val156Ala)
2g.174571960A>TCA349341479WIPF1c.845T>A (p.Val282Asp)
n.850T>A
c.467T>A (p.Val156Asp)
2g.174571961C>ACA349341481WIPF1c.844G>T (p.Val282Phe)
n.849G>T
c.466G>T (p.Val156Phe)
2g.174571961C>GCA349341483WIPF1c.844G>C (p.Val282Leu)
n.849G>C
c.466G>C (p.Val156Leu)
2g.174571961C>TCA349341485WIPF1c.844G>A (p.Val282Ile)
n.849G>A
c.466G>A (p.Val156Ile)
2g.174571962C>ACA430228686WIPF1c.843G>T (p.Ala281=)
n.848G>T
c.465G>T (p.Ala155=)
ClinVar dbSNP gnomAD v4
2g.174571962C=CA1308757377WIPF1c.843G= (p.Ala281=)
n.848G=
c.465G= (p.Ala155=)
2g.174571962C>GCA1974051WIPF1c.843G>C (p.Ala281=)
n.848G>C
c.465G>C (p.Ala155=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.174571962C>TCA1974052WIPF1c.843G>A (p.Ala281=)
n.848G>A
c.465G>A (p.Ala155=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.174571963G>ACA349341491WIPF1c.842C>T (p.Ala281Val)
n.847C>T
c.464C>T (p.Ala155Val)
gnomAD v4 COSMIC COSMIC COSMIC
2g.174571963G>CCA349341489WIPF1c.842C>G (p.Ala281Gly)
n.847C>G
c.464C>G (p.Ala155Gly)
2g.174571963G>TCA349341490WIPF1c.842C>A (p.Ala281Glu)
n.847C>A
c.464C>A (p.Ala155Glu)
2g.174571964C>ACA349341492WIPF1c.841G>T (p.Ala281Ser)
n.846G>T
c.463G>T (p.Ala155Ser)
2g.174571964C=CA1308757378WIPF1c.841G= (p.Ala281=)
n.846G=
c.463G= (p.Ala155=)
2g.174571964C>GCA1974053WIPF1c.841G>C (p.Ala281Pro)
n.846G>C
c.463G>C (p.Ala155Pro)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.174571964C>TCA349341493WIPF1c.841G>A (p.Ala281Thr)
n.846G>A
c.463G>A (p.Ala155Thr)
2g.174571965T>ACA349341495WIPF1c.840A>T (p.Glu280Asp)
n.845A>T
c.462A>T (p.Glu154Asp)
2g.174571965T>CCA430228690WIPF1c.840A>G (p.Glu280=)
n.845A>G
c.462A>G (p.Glu154=)
gnomAD v4
2g.174571965T>GCA349341497WIPF1c.840A>C (p.Glu280Asp)
n.845A>C
c.462A>C (p.Glu154Asp)
2g.174571966T>ACA349341500WIPF1c.839A>T (p.Glu280Val)
n.844A>T
c.461A>T (p.Glu154Val)
2g.174571966T>CCA349341502WIPF1c.839A>G (p.Glu280Gly)
n.844A>G
c.461A>G (p.Glu154Gly)
gnomAD v4
2g.174571966T>GCA349341504WIPF1c.839A>C (p.Glu280Ala)
n.844A>C
c.461A>C (p.Glu154Ala)
2g.174571967C>ACA349341505WIPF1c.838G>T (p.Glu280Ter)
n.843G>T
c.460G>T (p.Glu154Ter)
2g.174571967C>GCA349341507WIPF1c.838G>C (p.Glu280Gln)
n.843G>C
c.460G>C (p.Glu154Gln)
2g.174571967C>TCA349341509WIPF1c.838G>A (p.Glu280Lys)
n.843G>A
c.460G>A (p.Glu154Lys)
2g.174571968C>ACA349341511WIPF1c.837G>T (p.Arg279Ser)
n.842G>T
c.459G>T (p.Arg153Ser)
2g.174571968C=CA1308757379WIPF1c.837G= (p.Arg279=)
n.842G=
c.459G= (p.Arg153=)
2g.174571968C>GCA349341512WIPF1c.837G>C (p.Arg279Ser)
n.842G>C
c.459G>C (p.Arg153Ser)
2g.174571968C>TCA430228695WIPF1c.837G>A (p.Arg279=)
n.842G>A
c.459G>A (p.Arg153=)
dbSNP
2g.174571969C>ACA349341514WIPF1c.836G>T (p.Arg279Met)
n.841G>T
c.458G>T (p.Arg153Met)
2g.174571969C>GCA349341516WIPF1c.836G>C (p.Arg279Thr)
n.841G>C
c.458G>C (p.Arg153Thr)
2g.174571969C>TCA349341518WIPF1c.836G>A (p.Arg279Lys)
n.841G>A
c.458G>A (p.Arg153Lys)
gnomAD v4
2g.174571970T>ACA349341520WIPF1c.835A>T (p.Arg279Trp)
n.840A>T
c.457A>T (p.Arg153Trp)
2g.174571970T>CCA349341521WIPF1c.835A>G (p.Arg279Gly)
n.840A>G
c.457A>G (p.Arg153Gly)
2g.174571970T>GCA430228698WIPF1c.835A>C (p.Arg279=)
n.840A>C
c.457A>C (p.Arg153=)
2g.174571971G>ACA430228699WIPF1c.834C>T (p.His278=)
n.839C>T
c.456C>T (p.His152=)
gnomAD v4
2g.174571971G>CCA349341524WIPF1c.834C>G (p.His278Gln)
n.839C>G
c.456C>G (p.His152Gln)
2g.174571971G>TCA349341526WIPF1c.834C>A (p.His278Gln)
n.839C>A
c.456C>A (p.His152Gln)
2g.174571972T>ACA349341528WIPF1c.833A>T (p.His278Leu)
n.838A>T
c.455A>T (p.His152Leu)
2g.174571972T>CCA349341530WIPF1c.833A>G (p.His278Arg)
n.838A>G
c.455A>G (p.His152Arg)
dbSNP gnomAD v3 gnomAD v4
2g.174571972T>GCA349341531WIPF1c.833A>C (p.His278Pro)
n.838A>C
c.455A>C (p.His152Pro)
2g.174571972T=CA1308757380WIPF1c.833A= (p.His278=)
n.838A=
c.455A= (p.His152=)
2g.174571973G>ACA349341533WIPF1c.832C>T (p.His278Tyr)
n.837C>T
c.454C>T (p.His152Tyr)
2g.174571973G>CCA349341535WIPF1c.832C>G (p.His278Asp)
n.837C>G
c.454C>G (p.His152Asp)
2g.174571973G>TCA349341537WIPF1c.832C>A (p.His278Asn)
n.837C>A
c.454C>A (p.His152Asn)
2g.174571974G>ACA430228704WIPF1c.831C>T (p.Ile277=)
n.836C>T
c.453C>T (p.Ile151=)
2g.174571974G>CCA349341539WIPF1c.831C>G (p.Ile277Met)
n.836C>G
c.453C>G (p.Ile151Met)
2g.174571974G>TCA430228703WIPF1c.831C>A (p.Ile277=)
n.836C>A
c.453C>A (p.Ile151=)
gnomAD v4
2g.174571975A>CCA349341541WIPF1c.830T>G (p.Ile277Ser)
n.835T>G
c.452T>G (p.Ile151Ser)
gnomAD v4
2g.174571975A>GCA349341543WIPF1c.830T>C (p.Ile277Thr)
n.835T>C
c.452T>C (p.Ile151Thr)
2g.174571975A>TCA349341546WIPF1c.830T>A (p.Ile277Asn)
n.835T>A
c.452T>A (p.Ile151Asn)
gnomAD v4
2g.174571976T>ACA349341548WIPF1c.829A>T (p.Ile277Phe)
n.834A>T
c.451A>T (p.Ile151Phe)
2g.174571976T>CCA60843307WIPF1c.829A>G (p.Ile277Val)
n.834A>G
c.451A>G (p.Ile151Val)
dbSNP COSMIC COSMIC COSMIC
2g.174571976T>GCA349341554WIPF1c.829A>C (p.Ile277Leu)
n.834A>C
c.451A>C (p.Ile151Leu)
2g.174571976T=CA1308757381WIPF1c.829A= (p.Ile277=)
n.834A=
c.451A= (p.Ile151=)
2g.174571977G>ACA430228708WIPF1c.828C>T (p.Ser276=)
n.833C>T
c.450C>T (p.Ser150=)
dbSNP gnomAD v3 gnomAD v4
2g.174571977G>CCA430228709WIPF1c.828C>G (p.Ser276=)
n.833C>G
c.450C>G (p.Ser150=)
2g.174571977G=CA1308757382WIPF1c.828C= (p.Ser276=)
n.833C=
c.450C= (p.Ser150=)
2g.174571977G>TCA430228710WIPF1c.828C>A (p.Ser276=)
n.833C>A
c.450C>A (p.Ser150=)
2g.174571978G>ACA1974055WIPF1c.827C>T (p.Ser276Phe)
n.832C>T
c.449C>T (p.Ser150Phe)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.174571978G>CCA1974054WIPF1c.827C>G (p.Ser276Cys)
n.832C>G
c.449C>G (p.Ser150Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.174571978G=CA1308757383WIPF1c.827C= (p.Ser276=)
n.832C=
c.449C= (p.Ser150=)
2g.174571978G>TCA349341558WIPF1c.827C>A (p.Ser276Tyr)
n.832C>A
c.449C>A (p.Ser150Tyr)
2g.174571979A>CCA349341561WIPF1c.826T>G (p.Ser276Ala)
n.831T>G
c.448T>G (p.Ser150Ala)
2g.174571979A>GCA349341563WIPF1c.826T>C (p.Ser276Pro)
n.831T>C
c.448T>C (p.Ser150Pro)
gnomAD v4
2g.174571979A>TCA349341565WIPF1c.826T>A (p.Ser276Thr)
n.831T>A
c.448T>A (p.Ser150Thr)
2g.174571980G>ACA430228712WIPF1c.825C>T (p.Pro275=)
n.830C>T
c.447C>T (p.Pro149=)
gnomAD v4
2g.174571980G>CCA430228713WIPF1c.825C>G (p.Pro275=)
n.830C>G
c.447C>G (p.Pro149=)
2g.174571980G>TCA430228715WIPF1c.825C>A (p.Pro275=)
n.830C>A
c.447C>A (p.Pro149=)
2g.174571981G>ACA349341570WIPF1c.824C>T (p.Pro275Leu)
n.829C>T
c.446C>T (p.Pro149Leu)
gnomAD v4
2g.174571981G>CCA349341572WIPF1c.824C>G (p.Pro275Arg)
n.829C>G
c.446C>G (p.Pro149Arg)
2g.174571981G>TCA349341568WIPF1c.824C>A (p.Pro275His)
n.829C>A
c.446C>A (p.Pro149His)
2g.174571982G>ACA349341577WIPF1c.823C>T (p.Pro275Ser)
n.828C>T
c.445C>T (p.Pro149Ser)
2g.174571982G>CCA349341575WIPF1c.823C>G (p.Pro275Ala)
n.828C>G
c.445C>G (p.Pro149Ala)
2g.174571982G>TCA349341576WIPF1c.823C>A (p.Pro275Thr)
n.828C>A
c.445C>A (p.Pro149Thr)
gnomAD v4
2g.174571983C>ACA349341579WIPF1c.822G>T (p.Arg274Ser)
n.827G>T
c.444G>T (p.Arg148Ser)
gnomAD v4
2g.174571983C=CA1308757384WIPF1c.822G= (p.Arg274=)
n.827G=
c.444G= (p.Arg148=)
2g.174571983C>GCA349341580WIPF1c.822G>C (p.Arg274Ser)
n.827G>C
c.444G>C (p.Arg148Ser)
2g.174571983C>TCA430228720WIPF1c.822G>A (p.Arg274=)
n.827G>A
c.444G>A (p.Arg148=)
dbSNP gnomAD v4
2g.174571984C>ACA349341583WIPF1c.821G>T (p.Arg274Met)
n.826G>T
c.443G>T (p.Arg148Met)
gnomAD v4
2g.174571984C>GCA349341585WIPF1c.821G>C (p.Arg274Thr)
n.826G>C
c.443G>C (p.Arg148Thr)
2g.174571984C>TCA349341587WIPF1c.821G>A (p.Arg274Lys)
n.826G>A
c.443G>A (p.Arg148Lys)
2g.174571985T>ACA349341589WIPF1c.820A>T (p.Arg274Trp)
n.825A>T
c.442A>T (p.Arg148Trp)
2g.174571985T>CCA60843328WIPF1c.820A>G (p.Arg274Gly)
n.825A>G
c.442A>G (p.Arg148Gly)
dbSNP gnomAD v4
2g.174571985T>GCA430228722WIPF1c.820A>C (p.Arg274=)
n.825A>C
c.442A>C (p.Arg148=)
2g.174571985T=CA1308757385WIPF1c.820A= (p.Arg274=)
n.825A=
c.442A= (p.Arg148=)
2g.174571986G>ACA1974056WIPF1c.819C>T (p.Asn273=)
n.824C>T
c.441C>T (p.Asn147=)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.174571986G>CCA349341592WIPF1c.819C>G (p.Asn273Lys)
n.824C>G
c.441C>G (p.Asn147Lys)
dbSNP
2g.174571986G=CA1308757386WIPF1c.819C= (p.Asn273=)
n.824C=
c.441C= (p.Asn147=)
2g.174571986G>TCA349341594WIPF1c.819C>A (p.Asn273Lys)
n.824C>A
c.441C>A (p.Asn147Lys)
2g.174571987T>ACA349341601WIPF1c.818A>T (p.Asn273Ile)
n.823A>T
c.440A>T (p.Asn147Ile)
2g.174571987T>CCA349341599WIPF1c.818A>G (p.Asn273Ser)
n.823A>G
c.440A>G (p.Asn147Ser)
2g.174571987T>GCA349341597WIPF1c.818A>C (p.Asn273Thr)
n.823A>C
c.440A>C (p.Asn147Thr)
2g.174571988T>ACA349341603WIPF1c.817A>T (p.Asn273Tyr)
n.822A>T
c.439A>T (p.Asn147Tyr)
2g.174571988T>CCA349341605WIPF1c.817A>G (p.Asn273Asp)
n.822A>G
c.439A>G (p.Asn147Asp)
2g.174571988T>GCA349341607WIPF1c.817A>C (p.Asn273His)
n.822A>C
c.439A>C (p.Asn147His)
gnomAD v4
2g.174571989G>ACA430228728WIPF1c.816C>T (p.Gly272=)
n.821C>T
c.438C>T (p.Gly146=)
2g.174571989G>CCA430228729WIPF1c.816C>G (p.Gly272=)
n.821C>G
c.438C>G (p.Gly146=)
2g.174571989G>TCA430228730WIPF1c.816C>A (p.Gly272=)
n.821C>A
c.438C>A (p.Gly146=)
2g.174571990C>ACA349341609WIPF1c.815G>T (p.Gly272Val)
n.820G>T
c.437G>T (p.Gly146Val)
gnomAD v4
2g.174571990C=CA1308757387WIPF1c.815G= (p.Gly272=)
n.820G=
c.437G= (p.Gly146=)
2g.174571990C>GCA349341611WIPF1c.815G>C (p.Gly272Ala)
n.820G>C
c.437G>C (p.Gly146Ala)
2g.174571990C>TCA1974057WIPF1c.815G>A (p.Gly272Asp)
n.820G>A
c.437G>A (p.Gly146Asp)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.174571991C>ACA349341613WIPF1c.814G>T (p.Gly272Cys)
n.819G>T
c.436G>T (p.Gly146Cys)
2g.174571991C>GCA349341615WIPF1c.814G>C (p.Gly272Arg)
n.819G>C
c.436G>C (p.Gly146Arg)
2g.174571991C>TCA349341617WIPF1c.814G>A (p.Gly272Ser)
n.819G>A
c.436G>A (p.Gly146Ser)
2g.174571992C>ACA430228733WIPF1c.813G>T (p.Val271=)
n.818G>T
c.435G>T (p.Val145=)
gnomAD v4
2g.174571992C=CA1308757388WIPF1c.813G= (p.Val271=)
n.818G=
c.435G= (p.Val145=)
2g.174571992C>GCA430228735WIPF1c.813G>C (p.Val271=)
n.818G>C
c.435G>C (p.Val145=)
2g.174571992C>TCA430228736WIPF1c.813G>A (p.Val271=)
n.818G>A
c.435G>A (p.Val145=)
dbSNP
2g.174571993A=CA1308757389WIPF1c.812T= (p.Val271=)
n.817T=
c.434T= (p.Val145=)
2g.174571993A>CCA349341619WIPF1c.812T>G (p.Val271Gly)
n.817T>G
c.434T>G (p.Val145Gly)
2g.174571993A>GCA349341621WIPF1c.812T>C (p.Val271Ala)
n.817T>C
c.434T>C (p.Val145Ala)
dbSNP
2g.174571993A>TCA349341623WIPF1c.812T>A (p.Val271Glu)
n.817T>A
c.434T>A (p.Val145Glu)
2g.174571994C>ACA349341630WIPF1c.811G>T (p.Val271Leu)
n.816G>T
c.433G>T (p.Val145Leu)
2g.174571994C=CA1308757390WIPF1c.811G= (p.Val271=)
n.816G=
c.433G= (p.Val145=)
2g.174571994C>GCA349341628WIPF1c.811G>C (p.Val271Leu)
n.816G>C
c.433G>C (p.Val145Leu)
ClinVar dbSNP gnomAD v4
2g.174571994C>TCA349341625WIPF1c.811G>A (p.Val271Met)
n.816G>A
c.433G>A (p.Val145Met)
ClinVar dbSNP
2g.174571995T>ACA430228739WIPF1c.810A>T (p.Pro270=)
n.815A>T
c.432A>T (p.Pro144=)
2g.174571995T>CCA1974058WIPF1c.810A>G (p.Pro270=)
n.815A>G
c.432A>G (p.Pro144=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.174571995T>GCA430228740WIPF1c.810A>C (p.Pro270=)
n.815A>C
c.432A>C (p.Pro144=)
2g.174571995T=CA1308757391WIPF1c.810A= (p.Pro270=)
n.815A=
c.432A= (p.Pro144=)
2g.174571996G>ACA349341632WIPF1c.809C>T (p.Pro270Leu)
n.814C>T
c.431C>T (p.Pro144Leu)
dbSNP
2g.174571996G>CCA349341634WIPF1c.809C>G (p.Pro270Arg)
n.814C>G
c.431C>G (p.Pro144Arg)
2g.174571996G=CA1308757392WIPF1c.809C= (p.Pro270=)
n.814C=
c.431C= (p.Pro144=)
2g.174571996G>TCA349341636WIPF1c.809C>A (p.Pro270Gln)
n.814C>A
c.431C>A (p.Pro144Gln)
2g.174572001_174572003delCA537975061WIPF1c.807_809del (p.Pro270del)
n.812_814del
c.429_431del (p.Pro144del)
gnomAD v2
2g.174571997G>ACA349341638WIPF1c.808C>T (p.Pro270Ser)
n.813C>T
c.430C>T (p.Pro144Ser)
2g.174571997G>CCA349341640WIPF1c.808C>G (p.Pro270Ala)
n.813C>G
c.430C>G (p.Pro144Ala)
2g.174571997G>TCA349341642WIPF1c.808C>A (p.Pro270Thr)
n.813C>A
c.430C>A (p.Pro144Thr)
2g.174571998A>CCA430228744WIPF1c.807T>G (p.Pro269=)
n.812T>G
c.429T>G (p.Pro143=)
2g.174571998A>GCA430228745WIPF1c.807T>C (p.Pro269=)
n.812T>C
c.429T>C (p.Pro143=)
2g.174571998A>TCA430228746WIPF1c.807T>A (p.Pro269=)
n.812T>A
c.429T>A (p.Pro143=)
2g.174571999G>ACA349341644WIPF1c.806C>T (p.Pro269Leu)
n.811C>T
c.428C>T (p.Pro143Leu)
gnomAD v4
2g.174571999G>CCA349341646WIPF1c.806C>G (p.Pro269Arg)
n.811C>G
c.428C>G (p.Pro143Arg)
2g.174571999G>TCA349341648WIPF1c.806C>A (p.Pro269His)
n.811C>A
c.428C>A (p.Pro143His)
2g.174572000G>ACA349341650WIPF1c.805C>T (p.Pro269Ser)
n.810C>T
c.427C>T (p.Pro143Ser)
gnomAD v4 COSMIC COSMIC COSMIC
2g.174572000G>CCA349341651WIPF1c.805C>G (p.Pro269Ala)
n.810C>G
c.427C>G (p.Pro143Ala)
2g.174572000G>TCA349341653WIPF1c.805C>A (p.Pro269Thr)
n.810C>A
c.427C>A (p.Pro143Thr)
2g.174572001A>CCA430228749WIPF1c.804T>G (p.Pro268=)
n.809T>G
c.426T>G (p.Pro142=)
2g.174572001A>GCA430228751WIPF1c.804T>C (p.Pro268=)
n.809T>C
c.426T>C (p.Pro142=)
2g.174572001A>TCA430228750WIPF1c.804T>A (p.Pro268=)
n.809T>A
c.426T>A (p.Pro142=)
2g.174572002G>ACA349341659WIPF1c.803C>T (p.Pro268Leu)
n.808C>T
c.425C>T (p.Pro142Leu)
gnomAD v4
2g.174572002G>CCA349341656WIPF1c.803C>G (p.Pro268Arg)
n.808C>G
c.425C>G (p.Pro142Arg)
2g.174572002G>TCA349341658WIPF1c.803C>A (p.Pro268His)
n.808C>A
c.425C>A (p.Pro142His)
gnomAD v4
2g.174572003G>ACA349341661WIPF1c.802C>T (p.Pro268Ser)
n.807C>T
c.424C>T (p.Pro142Ser)
gnomAD v4
2g.174572003G>CCA349341663WIPF1c.802C>G (p.Pro268Ala)
n.807C>G
c.424C>G (p.Pro142Ala)
2g.174572003G=CA1308757393WIPF1c.802C= (p.Pro268=)
n.807C=
c.424C= (p.Pro142=)
2g.174572003G>TCA349341665WIPF1c.802C>A (p.Pro268Thr)
n.807C>A
c.424C>A (p.Pro142Thr)
dbSNP gnomAD v3 gnomAD v4
2g.174572004T>ACA430228755WIPF1c.801A>T (p.Pro267=)
n.806A>T
c.423A>T (p.Pro141=)
2g.174572004T>CCA430228754WIPF1c.801A>G (p.Pro267=)
n.806A>G
c.423A>G (p.Pro141=)
2g.174572004T>GCA430228753WIPF1c.801A>C (p.Pro267=)
n.806A>C
c.423A>C (p.Pro141=)
dbSNP gnomAD v3 gnomAD v4
2g.174572004T=CA1308757394WIPF1c.801A= (p.Pro267=)
n.806A=
c.423A= (p.Pro141=)
2g.174572005G>ACA349341667WIPF1c.800C>T (p.Pro267Leu)
n.805C>T
c.422C>T (p.Pro141Leu)
gnomAD v4
2g.174572005G>CCA349341669WIPF1c.800C>G (p.Pro267Arg)
n.805C>G
c.422C>G (p.Pro141Arg)
2g.174572005G>TCA349341671WIPF1c.800C>A (p.Pro267Gln)
n.805C>A
c.422C>A (p.Pro141Gln)
2g.174572006G>ACA349341673WIPF1c.799C>T (p.Pro267Ser)
n.804C>T
c.421C>T (p.Pro141Ser)
dbSNP gnomAD v4
2g.174572006G>CCA349341675WIPF1c.799C>G (p.Pro267Ala)
n.804C>G
c.421C>G (p.Pro141Ala)
2g.174572006G=CA1308757395WIPF1c.799C= (p.Pro267=)
n.804C=
c.421C= (p.Pro141=)
2g.174572006G>TCA349341677WIPF1c.799C>A (p.Pro267Thr)
n.804C>A
c.421C>A (p.Pro141Thr)
2g.174572007T>ACA430228756WIPF1c.798A>T (p.Pro266=)
n.803A>T
c.420A>T (p.Pro140=)
2g.174572007T>CCA1974059WIPF1c.798A>G (p.Pro266=)
n.803A>G
c.420A>G (p.Pro140=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.174572007T>GCA430228757WIPF1c.798A>C (p.Pro266=)
n.803A>C
c.420A>C (p.Pro140=)
dbSNP
2g.174572007T=CA1308757396WIPF1c.798A= (p.Pro266=)
n.803A=
c.420A= (p.Pro140=)
2g.174572008G>ACA349341680WIPF1c.797C>T (p.Pro266Leu)
n.802C>T
c.419C>T (p.Pro140Leu)
dbSNP gnomAD v2
2g.174572008G>CCA349341682WIPF1c.797C>G (p.Pro266Arg)
n.802C>G
c.419C>G (p.Pro140Arg)
2g.174572008G=CA1308757397WIPF1c.797C= (p.Pro266=)
n.802C=
c.419C= (p.Pro140=)
2g.174572008G>TCA349341684WIPF1c.797C>A (p.Pro266Gln)
n.802C>A
c.419C>A (p.Pro140Gln)
2g.174572009G>ACA349341688WIPF1c.796C>T (p.Pro266Ser)
n.801C>T
c.418C>T (p.Pro140Ser)
2g.174572009G>CCA349341690WIPF1c.796C>G (p.Pro266Ala)
n.801C>G
c.418C>G (p.Pro140Ala)
2g.174572009G>TCA349341686WIPF1c.796C>A (p.Pro266Thr)
n.801C>A
c.418C>A (p.Pro140Thr)
2g.174572010A>CCA430228758WIPF1c.795T>G (p.Pro265=)
n.800T>G
c.417T>G (p.Pro139=)
2g.174572010A>GCA430228759WIPF1c.795T>C (p.Pro265=)
n.800T>C
c.417T>C (p.Pro139=)
2g.174572010A>TCA430228760WIPF1c.795T>A (p.Pro265=)
n.800T>A
c.417T>A (p.Pro139=)
2g.174572011G>ACA349341692WIPF1c.794C>T (p.Pro265Leu)
n.799C>T
c.416C>T (p.Pro139Leu)
dbSNP
2g.174572011G>CCA349341694WIPF1c.794C>G (p.Pro265Arg)
n.799C>G
c.416C>G (p.Pro139Arg)
2g.174572011G=CA1308757398WIPF1c.794C= (p.Pro265=)
n.799C=
c.416C= (p.Pro139=)
2g.174572011G>TCA349341696WIPF1c.794C>A (p.Pro265His)
n.799C>A
c.416C>A (p.Pro139His)
2g.174572015delCA2662015915WIPF1c.794del (p.Pro265LeufsTer?)
n.799del
c.416del (p.Pro139LeufsTer?)
gnomAD v4
2g.174572012G>ACA349341697WIPF1c.793C>T (p.Pro265Ser)
n.798C>T
c.415C>T (p.Pro139Ser)
2g.174572012G>CCA349341698WIPF1c.793C>G (p.Pro265Ala)
n.798C>G
c.415C>G (p.Pro139Ala)
2g.174572012G>TCA349341700WIPF1c.793C>A (p.Pro265Thr)
n.798C>A
c.415C>A (p.Pro139Thr)

Number of alleles fetched