Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.48965198_48965246delCA2586287852FTLc.201_249del (p.Ala68GlufsTer?)
gnomAD v4
19g.48965225_48965263delCA2586287878FTLc.228_266del (p.Arg77_Arg89del)
gnomAD v4
19g.48965244C>GCA2586287896FTLc.247C>G (p.Pro83Ala)
gnomAD v4
19g.48965246C>GCA2586287897FTLc.249C>G (p.Pro83=)
gnomAD v4
19g.48965247C>ACA2586287898FTLc.250C>A (p.Arg84=)
gnomAD v4
19g.48965247C=CA2340161080FTLc.250C= (p.Arg84=)
19g.48965247C>GCA309374797FTLc.250C>G (p.Arg84Gly)
dbSNP gnomAD v3 gnomAD v4
19g.48965247C>TCA2586287899FTLc.250C>T (p.Arg84Ter)
gnomAD v4
19g.48965248G>ACA2814670074FTLc.251G>A (p.Arg84Gln)
19g.48965248G>TCA2586287900FTLc.251G>T (p.Arg84Leu)
gnomAD v4
19g.48965250G>ACA2586287901FTLc.253G>A (p.Ala85Thr)
gnomAD v4
19g.48965250G>TCA2586287902FTLc.253G>T (p.Ala85Ser)
gnomAD v4
19g.48965251C>TCA2586287903FTLc.254C>T (p.Ala85Val)
gnomAD v4
19g.48965252G>ACA2586287905FTLc.255G>A (p.Ala85=)
gnomAD v4
19g.48965255_48965269delCA2586287904FTLc.258_272del (p.Cys87_Pro91del)
gnomAD v4
19g.48965253C=CA2340161082FTLc.256C= (p.Pro86=)
19g.48965253C>TCA996657252FTLc.256C>T (p.Pro86Ser)
dbSNP gnomAD v3 gnomAD v4
19g.48965254C>ACA2586287906FTLc.257C>A (p.Pro86His)
gnomAD v4
19g.48965256T>CCA2586287907FTLc.259T>C (p.Cys87Arg)
gnomAD v4
19g.48965257G>ACA2586287908FTLc.260G>A (p.Cys87Tyr)
gnomAD v4
19g.48965257G>TCA2586287909FTLc.260G>T (p.Cys87Phe)
gnomAD v4
19g.48965259C>ACA2586287910FTLc.262C>A (p.Leu88Ile)
gnomAD v4
19g.48965259C=CA2340161083FTLc.262C= (p.Leu88=)
19g.48965259C>GCA309374806FTLc.262C>G (p.Leu88Val)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.48965259C>TCA2586287911FTLc.262C>T (p.Leu88Phe)
gnomAD v4
19g.48965260T>CCA2586287912FTLc.263T>C (p.Leu88Pro)
gnomAD v4
19g.48965260T>GCA309374807FTLc.263T>G (p.Leu88Arg)
dbSNP gnomAD v3 gnomAD v4
19g.48965260T=CA2340161085FTLc.263T= (p.Leu88=)
19g.48965261C=CA2340161087FTLc.264C= (p.Leu88=)
19g.48965261C>TCA2340161088FTLc.264C>T (p.Leu88=)
dbSNP
19g.48965262C>ACA2586287913FTLc.265C>A (p.Arg89=)
gnomAD v4
19g.48965262C>TCA2586287914FTLc.265C>T (p.Arg89Ter)
gnomAD v4
19g.48965263G>ACA883052034FTLc.266G>A (p.Arg89Gln)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.48965263G>CCA309374808FTLc.266G>C (p.Arg89Pro)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.48965263G=CA2340161090FTLc.266G= (p.Arg89=)
19g.48965263G>TCA2586287915FTLc.266G>T (p.Arg89Leu)
gnomAD v4
19g.48965265G>TCA2586287917FTLc.268G>T (p.Gly90Trp)
gnomAD v4
19g.48965267delCA2586287916FTLc.270del (p.Pro91ArgfsTer?)
gnomAD v4
19g.48965266G>TCA2586287918FTLc.269G>T (p.Gly90Val)
gnomAD v4
19g.48965267G>ACA2586287919FTLc.270G>A (p.Gly90=)
gnomAD v4
19g.48965267G=CA2340161091FTLc.270G= (p.Gly90=)
19g.48965267G>TCA2340161092FTLc.270G>T (p.Gly90=)
dbSNP
19g.48965268C>ACA2586287920FTLc.271C>A (p.Pro91Thr)
gnomAD v4
19g.48965268C>TCA2586287921FTLc.271C>T (p.Pro91Ser)
gnomAD v4
19g.48965269C>ACA2586287922FTLc.272C>A (p.Pro91Gln)
gnomAD v4
19g.48965269C=CA2340161094FTLc.272C= (p.Pro91=)
19g.48965269C>TCA996657261FTLc.272C>T (p.Pro91Leu)
dbSNP gnomAD v3 gnomAD v4
19g.48965270G>ACA2586287923FTLc.273G>A (p.Pro91=)
dbSNP gnomAD v4
19g.48965270G>CCA2740096955FTLc.273G>C (p.Pro91=)
ClinVar
19g.48965270G>TCA2586287924FTLc.273G>T (p.Pro91=)
gnomAD v4
19g.48965271G>ACA2340161096FTLc.274G>A (p.Ala92Thr)
dbSNP gnomAD v4
19g.48965271G=CA2340161095FTLc.274G= (p.Ala92=)
19g.48965272C>ACA2586287925FTLc.275C>A (p.Ala92Glu)
gnomAD v4
19g.48965272C=CA2340161097FTLc.275C= (p.Ala92=)
19g.48965272C>TCA883052035FTLc.275C>T (p.Ala92Val)
dbSNP gnomAD v4
19g.48965273G>ACA2586287926FTLc.276G>A (p.Ala92=)
gnomAD v4
19g.48965273G>TCA2586287927FTLc.276G>T (p.Ala92=)
gnomAD v4
19g.48965276C>TCA2586287928FTLc.279C>T (p.His93=)
gnomAD v4
19g.48965277C>ACA2586287929FTLc.280C>A (p.His94Asn)
gnomAD v4
19g.48965277C=CA2340161098FTLc.280C= (p.His94=)
19g.48965277C>TCA309374813FTLc.280C>T (p.His94Tyr)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.48965278A=CA2340161099FTLc.281A= (p.His94=)
19g.48965278A>GCA2340161100FTLc.281A>G (p.His94Arg)
dbSNP
19g.48965279T>CCA2586287930FTLc.282T>C (p.His94=)
gnomAD v4
19g.48965280A>TCA2586287931FTLc.283A>T (p.Lys95Ter)
gnomAD v4
19g.48965281A>GCA2586287932FTLc.284A>G (p.Lys95Arg)
gnomAD v4
19g.48965283A>GCA2586287933FTLc.286A>G (p.Arg96Gly)
gnomAD v4
19g.48965286A>GCA2586287934FTLc.289A>G (p.Ser97Gly)
gnomAD v4
19g.48965288_48965312delCA2695228961FTLc.291_315del (p.Arg98SerfsTer?)
19g.48965288C>ACA996657265FTLc.291C>A (p.Ser97Arg)
dbSNP gnomAD v4
19g.48965288C=CA2340161101FTLc.291C= (p.Ser97=)
19g.48965288C>TCA2586287935FTLc.291C>T (p.Ser97=)
gnomAD v4
19g.48965289C>ACA996657274FTLc.292C>A (p.Arg98Ser)
dbSNP gnomAD v3 gnomAD v4
19g.48965289C=CA2340161102FTLc.292C= (p.Arg98=)
19g.48965289C>TCA996657275FTLc.292C>T (p.Arg98Cys)
dbSNP gnomAD v3 gnomAD v4
19g.48965290G>ACA996657280FTLc.293G>A (p.Arg98His)
dbSNP gnomAD v3 gnomAD v4
19g.48965290G>CCA633889467FTLc.293G>C (p.Arg98Pro)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.48965290G=CA2340161103FTLc.293G= (p.Arg98=)
19g.48965290G>TCA2586287936FTLc.293G>T (p.Arg98Leu)
gnomAD v4
19g.48965291C=CA2340161104FTLc.294C= (p.Arg98=)
19g.48965291C>GCA2340161105FTLc.294C>G (p.Arg98=)
dbSNP
19g.48965293delCA2586287937FTLc.296del (p.Pro99LeufsTer?)
gnomAD v4
19g.48965292C>ACA2586287938FTLc.295C>A (p.Pro99Thr)
gnomAD v4
19g.48965292C=CA2340161107FTLc.295C= (p.Pro99=)
19g.48965292C>GCA2586287939FTLc.295C>G (p.Pro99Ala)
gnomAD v4
19g.48965292C>TCA883052036FTLc.295C>T (p.Pro99Ser)
dbSNP gnomAD v4
19g.48965293C=CA2340161109FTLc.296C= (p.Pro99=)
19g.48965293C>TCA309374819FTLc.296C>T (p.Pro99Leu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.48965294T>GCA883052037FTLc.297T>G (p.Pro99=)
dbSNP gnomAD v3 gnomAD v4
19g.48965294T=CA2340161111FTLc.297T= (p.Pro99=)
19g.48965295A=CA2340161112FTLc.298A= (p.Ser100=)
19g.48965295A>CCA309374820FTLc.298A>C (p.Ser100Arg)
dbSNP gnomAD v3 gnomAD v4
19g.48965295A>GCA2340161113FTLc.298A>G (p.Ser100Gly)
dbSNP gnomAD v4
19g.48965296G>ACA2340161115FTLc.299G>A (p.Ser100Asn)
dbSNP gnomAD v4
19g.48965296G=CA2340161114FTLc.299G= (p.Ser100=)
19g.48965296G>TCA2586287940FTLc.299G>T (p.Ser100Ile)
gnomAD v4
19g.48965297C>ACA883052039FTLc.300C>A (p.Ser100Arg)
dbSNP gnomAD v4
19g.48965297C=CA2340161116FTLc.300C= (p.Ser100=)
19g.48965297C>TCA2586287941FTLc.300C>T (p.Ser100=)
gnomAD v4
19g.48965298C>ACA2586287942FTLc.301C>A (p.His101Asn)
gnomAD v4
19g.48965298C=CA2340161117FTLc.301C= (p.His101=)
19g.48965298C>TCA996657291FTLc.301C>T (p.His101Tyr)
dbSNP gnomAD v3 gnomAD v4
19g.48965299A=CA2340161118FTLc.302A= (p.His101=)
19g.48965299A>GCA996657295FTLc.302A>G (p.His101Arg)
dbSNP gnomAD v3 gnomAD v4
19g.48965300C>ACA633889468FTLc.303C>A (p.His101Gln)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.48965300C=CA2340161119FTLc.303C= (p.His101=)
19g.48965300C>GCA2586287943FTLc.303C>G (p.His101Gln)
gnomAD v4
19g.48965300C>TCA2586287944FTLc.303C>T (p.His101=)
gnomAD v4
19g.48965301G>ACA309374828FTLc.-207G>A (n.-207G>A)
c.304G>A (p.Val102Ile)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.48965301G>CCA633889469FTLc.-207G>C (n.-207G>C)
c.304G>C (p.Val102Leu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.48965301G=CA2340161120FTLc.-207G= (n.-207G=)
c.304G= (p.Val102=)
19g.48965301G>TCA309374835FTLc.-207G>T (n.-207G>T)
c.304G>T (p.Val102Phe)
dbSNP gnomAD v4
19g.48965301dupCA2740096956FTLc.-207dup (n.-207dup)
c.304dup (p.Val102GlyfsTer?)
ClinVar
19g.48965302T>ACA883052048FTLc.-206T>A (n.-206T>A)
c.305T>A (p.Val102Asp)
dbSNP gnomAD v4
19g.48965302T>CCA2340161123FTLc.-206T>C (n.-206T>C)
c.305T>C (p.Val102Ala)
dbSNP gnomAD v4
19g.48965302T>GCA2586287945FTLc.-206T>G (n.-206T>G)
c.305T>G (p.Val102Gly)
gnomAD v4
19g.48965302T=CA2340161122FTLc.-206T= (n.-206T=)
c.305T= (p.Val102=)
19g.48965302_48965303delinsTCCA2340161121FTLc.-206_-205delinsTC (n.-206_-205delinsTC)
c.305_306delinsTC (p.Val102=)
19g.48965303C>ACA2586287946FTLc.-205C>A (n.-205C>A)
c.306C>A (p.Val102=)
gnomAD v4
19g.48965303C=CA2340161125FTLc.-205C= (n.-205C=)
c.306C= (p.Val102=)
19g.48965303C>TCA2340161124FTLc.-205C>T (n.-205C>T)
c.306C>T (p.Val102=)
ClinVar dbSNP gnomAD v4
19g.48965306dupCA883052050FTLc.-202dup (n.-202dup)
c.309dup (p.Ser104LeufsTer?)
dbSNP gnomAD v3 gnomAD v4
19g.48965306delCA309374857FTLc.-202del (n.-202del)
c.309del (p.Ser104ArgfsTer?)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.48965304C>ACA2586287947FTLc.-204C>A (n.-204C>A)
c.307C>A (p.Pro103Thr)
gnomAD v4
19g.48965304C>TCA2586287948FTLc.-204C>T (n.-204C>T)
c.307C>T (p.Pro103Ser)
gnomAD v4
19g.48965305C>ACA2586287949FTLc.-203C>A (n.-203C>A)
c.308C>A (p.Pro103His)
gnomAD v4
19g.48965305C=CA2340161126FTLc.-203C= (n.-203C=)
c.308C= (p.Pro103=)
19g.48965305C>TCA883052054FTLc.-203C>T (n.-203C>T)
c.308C>T (p.Pro103Leu)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.48965306C=CA2340161127FTLc.-202C= (n.-202C=)
c.309C= (p.Pro103=)
19g.48965306C>TCA883052055FTLc.-202C>T (n.-202C>T)
c.309C>T (p.Pro103=)
dbSNP gnomAD v3 gnomAD v4
19g.48965307T>CCA2586287950FTLc.-201T>C (n.-201T>C)
c.310T>C (p.Ser104Pro)
gnomAD v4
19g.48965308C>ACA2586287951FTLc.-200C>A (n.-200C>A)
c.311C>A (p.Ser104Ter)
gnomAD v4
19g.48965308C=CA2340161128FTLc.-200C= (n.-200C=)
c.311C= (p.Ser104=)
19g.48965308C>GCA309374868FTLc.-200C>G (n.-200C>G)
c.311C>G (p.Ser104Trp)
dbSNP gnomAD v3 gnomAD v4
19g.48965308C>TCA2586287952FTLc.-200C>T (n.-200C>T)
c.311C>T (p.Ser104Leu)
gnomAD v4
19g.48965309G>ACA309374872FTLc.-199G>A (n.-199G>A)
c.312G>A (p.Ser104=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.48965309G=CA2340161129FTLc.-199G= (n.-199G=)
c.312G= (p.Ser104=)
19g.48965309G>TCA2340161130FTLc.-199G>T (n.-199G>T)
c.312G>T (p.Ser104=)
dbSNP gnomAD v4
19g.48965310C=CA2340161131FTLc.-198C= (n.-198C=)
c.313C= (p.Gln105=)
19g.48965310C>TCA883052064FTLc.-198C>T (n.-198C>T)
c.313C>T (p.Gln105Ter)
dbSNP gnomAD v4
19g.48965311A=CA2340161132FTLc.-197A= (n.-197A=)
c.314A= (p.Gln105=)
19g.48965311A>GCA2586287953FTLc.-197A>G (n.-197A>G)
c.314A>G (p.Gln105Arg)
dbSNP gnomAD v4
19g.48965311A>TCA996657327FTLc.-197A>T (n.-197A>T)
c.314A>T (p.Gln105Leu)
dbSNP gnomAD v3 gnomAD v4
19g.48965312G>ACA2586287954FTLc.-196G>A (n.-196G>A)
c.315G>A (p.Gln105=)
gnomAD v4
19g.48965312G>CCA2340161134FTLc.-196G>C (n.-196G>C)
c.315G>C (p.Gln105His)
ClinVar dbSNP
19g.48965312G=CA2340161133FTLc.-196G= (n.-196G=)
c.315G= (p.Gln105=)
19g.48965312G>TCA2586287955FTLc.-196G>T (n.-196G>T)
c.315G>T (p.Gln105His)
gnomAD v4
19g.48965313T>GCA2586287956FTLc.-195T>G (n.-195T>G)
c.316T>G (p.Phe106Val)
gnomAD v4
19g.48965314T>ACA2340161136FTLc.-194T>A (n.-194T>A)
c.317T>A (p.Phe106Tyr)
dbSNP gnomAD v4
19g.48965314T>GCA2340161137FTLc.-194T>G (n.-194T>G)
c.317T>G (p.Phe106Cys)
dbSNP
19g.48965314T=CA2340161135FTLc.-194T= (n.-194T=)
c.317T= (p.Phe106=)
19g.48965315C>ACA2586287957FTLc.-193C>A (n.-193C>A)
c.318C>A (p.Phe106Leu)
gnomAD v4
19g.48965315C=CA2340161138FTLc.-193C= (n.-193C=)
c.318C= (p.Phe106=)
19g.48965315C>GCA2340161139FTLc.-193C>G (n.-193C>G)
c.318C>G (p.Phe106Leu)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.48965315C>TCA2340161140FTLc.-193C>T (n.-193C>T)
c.318C>T (p.Phe106=)
dbSNP gnomAD v4
19g.48965316G>ACA309374873FTLc.-192G>A (n.-192G>A)
c.319G>A (p.Gly107Ser)
dbSNP gnomAD v3 gnomAD v4
19g.48965316G=CA2340161141FTLc.-192G= (n.-192G=)
c.319G= (p.Gly107=)
19g.48965316G>TCA2586287958FTLc.-192G>T (n.-192G>T)
c.319G>T (p.Gly107Cys)
gnomAD v4
19g.48965317G>ACA2340161143FTLc.-191G>A (n.-191G>A)
c.320G>A (p.Gly107Asp)
dbSNP
19g.48965317G=CA2340161142FTLc.-191G= (n.-191G=)
c.320G= (p.Gly107=)
19g.48965317_48965346delinsGCGGTCCCGCGGGTCTGTCTCTTGCTTCAACA2340161144FTLc.-191_-162delinsGCGGTCCCGCGGGTCTGTCTCTTGCTTCAA (n.-191_-162delinsGCGGTCCCGCGGGTCTGTCTCTTGCTTCAA)
c.320_349delinsGCGGTCCCGCGGGTCTGTCTCTTGCTTCAA (p.Gly107=)
19g.48965318C>ACA2586287959FTLc.-190C>A (n.-190C>A)
c.321C>A (p.Gly107=)
gnomAD v4
19g.48965318C=CA2340161145FTLc.-190C= (n.-190C=)
c.321C= (p.Gly107=)
19g.48965318C>TCA883052074FTLc.-190C>T (n.-190C>T)
c.321C>T (p.Gly107=)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.48965319_48965347delCA126553FTLc.-189_-161del (n.-189_-161del)
c.322_350del (p.Gly108SerfsTer?)
ClinVar dbSNP
19g.48965319G>ACA2586287961FTLc.-189G>A (n.-189G>A)
c.322G>A (p.Gly108Ser)
gnomAD v4
19g.48965319G>CCA309374876FTLc.-189G>C (n.-189G>C)
c.322G>C (p.Gly108Arg)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.48965319G=CA2340161146FTLc.-189G= (n.-189G=)
c.322G= (p.Gly108=)
19g.48965319G>TCA883052079FTLc.-189G>T (n.-189G>T)
c.322G>T (p.Gly108Cys)
ClinVar dbSNP gnomAD v4
19g.48965320delCA2586287960FTLc.-188del (n.-188del)
c.323del (p.Gly108ValfsTer?)
gnomAD v4
19g.48965320G>ACA2586287962FTLc.-188G>A (n.-188G>A)
c.323G>A (p.Gly108Asp)
gnomAD v4
19g.48965321T>CCA2586287963FTLc.-187T>C (n.-187T>C)
c.324T>C (p.Gly108=)
gnomAD v4
19g.48965322C>ACA1139666526FTLc.-186C>A (n.-186C>A)
c.325C>A (p.Pro109Thr)
ClinVar dbSNP gnomAD v4
19g.48965322C=CA2340161147FTLc.-186C= (n.-186C=)
c.325C= (p.Pro109=)
19g.48965322C>GCA2586287964FTLc.-186C>G (n.-186C>G)
c.325C>G (p.Pro109Ala)
gnomAD v4
19g.48965322C>TCA309374877FTLc.-186C>T (n.-186C>T)
c.325C>T (p.Pro109Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.48965323C=CA2340161148FTLc.-185C= (n.-185C=)
c.326C= (p.Pro109=)
19g.48965323C>TCA309374884FTLc.-185C>T (n.-185C>T)
c.326C>T (p.Pro109Leu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.48965324C>ACA996657372FTLc.-184C>A (n.-184C>A)
c.327C>A (p.Pro109=)
dbSNP gnomAD v3 gnomAD v4
19g.48965324C=CA2340161149FTLc.-184C= (n.-184C=)
c.327C= (p.Pro109=)
19g.48965324C>GCA309374902FTLc.-184C>G (n.-184C>G)
c.327C>G (p.Pro109=)
ClinVar dbSNP gnomAD v4
19g.48965324C>TCA309374890FTLc.-184C>T (n.-184C>T)
c.327C>T (p.Pro109=)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.48965325G>ACA309374909FTLc.-183G>A (n.-183G>A)
c.328G>A (p.Ala110Thr)
dbSNP gnomAD v4
19g.48965325G>CCA2586287965FTLc.-183G>C (n.-183G>C)
c.328G>C (p.Ala110Pro)
gnomAD v4
19g.48965325G=CA2340161150FTLc.-183G= (n.-183G=)
c.328G= (p.Ala110=)
19g.48965325G>TCA2586287966FTLc.-183G>T (n.-183G>T)
c.328G>T (p.Ala110Ser)
gnomAD v4
19g.48965326C>ACA2586287967FTLc.-182C>A (n.-182C>A)
c.329C>A (p.Ala110Glu)
gnomAD v4
19g.48965326C=CA2340161151FTLc.-182C= (n.-182C=)
c.329C= (p.Ala110=)
19g.48965326C>TCA10575529FTLc.-182C>T (n.-182C>T)
c.329C>T (p.Ala110Val)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.[48965326C>T;48965330T>G]CA645373273FTLc.[-182C>T;-178T>G] (n.[-182C>T;-178T>G])
c.[329C>T;333T>G] (p.[Ala110Val;Gly111=])
19g.48965326_48965330delinsTGGGGCA2695228962FTLc.-182_-178delinsTGGGG (n.-182_-178delinsTGGGG)
c.329_333delinsTGGGG (p.Ala110Val)
19g.48965326_48965332delinsAGGGGCCCA2695228963FTLc.-182_-176delinsAGGGGCC (n.-182_-176delinsAGGGGCC)
c.329_335delinsAGGGGCC (p.Ala110_Leu112delinsGluGlyPro)
19g.48965327G>ACA2586287968FTLc.-181G>A (n.-181G>A)
c.330G>A (p.Ala110=)
ClinVar gnomAD v4
19g.48965327G>TCA2586287969FTLc.-181G>T (n.-181G>T)
c.330G>T (p.Ala110=)
gnomAD v4
19g.48965329delCA2735957910FTLc.-179del (n.-179del)
c.332del (p.Gly111ValfsTer?)
dbSNP
19g.48965328G>ACA2586287970FTLc.-180G>A (n.-180G>A)
c.331G>A (p.Gly111Ser)
gnomAD v4
19g.48965329G>ACA883052094FTLc.-179G>A (n.-179G>A)
c.332G>A (p.Gly111Asp)
ClinVar dbSNP gnomAD v4
19g.48965329G=CA2340161153FTLc.-179G= (n.-179G=)
c.332G= (p.Gly111=)
19g.48965329_48965335delinsGTCTGTCCA2340161152FTLc.-179_-173delinsGTCTGTC (n.-179_-173delinsGTCTGTC)
c.332_338delinsGTCTGTC (p.Gly111=)
19g.48965330T>CCA2586287971FTLc.-178T>C (n.-178T>C)
c.333T>C (p.Gly111=)
gnomAD v4
19g.48965330T>GCA10588904FTLc.-178T>G (n.-178T>G)
c.333T>G (p.Gly111=)
dbSNP
19g.48965330T=CA2340161154FTLc.-178T= (n.-178T=)
c.333T= (p.Gly111=)
19g.48965333_48965338delCA126558FTLc.-175_-170del (n.-175_-170del)
c.336_341del (p.Ser113_Leu114del)
ClinVar dbSNP
19g.48965331C>ACA2340161156FTLc.-177C>A (n.-177C>A)
c.334C>A (p.Leu112Met)
dbSNP
19g.48965331C=CA2340161155FTLc.-177C= (n.-177C=)
c.334C= (p.Leu112=)
19g.48965331C>TCA309374931FTLc.-177C>T (n.-177C>T)
c.334C>T (p.Leu112=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.48965332T>CCA2340161158FTLc.-176T>C (n.-176T>C)
c.335T>C (p.Leu112Pro)
dbSNP gnomAD v4
19g.48965332T>GCA2586287972FTLc.-176T>G (n.-176T>G)
c.335T>G (p.Leu112Arg)
gnomAD v4
19g.48965332T=CA2340161157FTLc.-176T= (n.-176T=)
c.335T= (p.Leu112=)
19g.48965333G>TCA2586287973FTLc.-175G>T (n.-175G>T)
c.336G>T (p.Leu112=)
gnomAD v4
19g.48965334T>ACA2580608363FTLc.-174T>A (n.-174T>A)
c.337T>A (p.Ser113Thr)
19g.48965334T>CCA309374937FTLc.-174T>C (n.-174T>C)
c.337T>C (p.Ser113Pro)
dbSNP
19g.48965334T>GCA2580608362FTLc.-174T>G (n.-174T>G)
c.337T>G (p.Ser113Ala)
19g.48965334T=CA2340161159FTLc.-174T= (n.-174T=)
c.337T= (p.Ser113=)
19g.48965335C>ACA883052107FTLc.-173C>A (n.-173C>A)
c.338C>A (p.Ser113Tyr)
dbSNP gnomAD v3 gnomAD v4
19g.48965335C=CA2340161160FTLc.-173C= (n.-173C=)
c.338C= (p.Ser113=)
19g.48965335C>GCA309374940FTLc.-173C>G (n.-173C>G)
c.338C>G (p.Ser113Cys)
ClinVar dbSNP gnomAD v4
19g.48965335C>TCA633889470FTLc.-173C>T (n.-173C>T)
c.338C>T (p.Ser113Phe)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.48965336T>CCA633889471FTLc.-172T>C (n.-172T>C)
c.339T>C (p.Ser113=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.48965336T=CA2340161161FTLc.-172T= (n.-172T=)
c.339T= (p.Ser113=)
19g.48965337C>GCA2695228964FTLc.-171C>G (n.-171C>G)
c.340C>G (p.Leu114Val)
19g.48965340_48965343delCA2695228965FTLc.-168_-165del (n.-168_-165del)
c.343_346del (p.Ala115GlnfsTer?)
19g.48965338T>CCA2573156629FTLc.-170T>C (n.-170T>C)
c.341T>C (p.Leu114Pro)
ClinVar dbSNP gnomAD v4
19g.48965339T>CCA2557813137FTLc.-169T>C (n.-169T>C)
c.342T>C (p.Leu114=)
gnomAD v4
19g.48965340G>ACA126552FTLc.-168G>A (n.-168G>A)
c.343G>A (p.Ala115Thr)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.48965340G>CCA126559FTLc.-168G>C (n.-168G>C)
c.343G>C (p.Ala115Pro)
ClinVar dbSNP gnomAD v4
19g.48965340G=CA2340161162FTLc.-168G= (n.-168G=)
c.343G= (p.Ala115=)
19g.48965340G>TCA126554FTLc.-168G>T (n.-168G>T)
c.343G>T (p.Ala115Ser)
ClinVar dbSNP
19g.48965341C>ACA2695228966FTLc.-167C>A (n.-167C>A)
c.344C>A (p.Ala115Asp)
19g.48965341C=CA2340161163FTLc.-167C= (n.-167C=)
c.344C= (p.Ala115=)
19g.48965341C>TCA1139666527FTLc.-167C>T (n.-167C>T)
c.344C>T (p.Ala115Val)
ClinVar dbSNP gnomAD v4
19g.48965342T>ACA2586287974FTLc.-166T>A (n.-166T>A)
c.345T>A (p.Ala115=)
gnomAD v4
19g.48965342T>CCA2499225536FTLc.-166T>C (n.-166T>C)
c.345T>C (p.Ala115=)
ClinVar dbSNP
19g.48965343T>CCA2586287976FTLc.-165T>C (n.-165T>C)
c.346T>C (p.Ser116Pro)
gnomAD v4
19g.48965343T>GCA2586287975FTLc.-165T>G (n.-165T>G)
c.346T>G (p.Ser116Ala)
gnomAD v4
19g.48965344C>ACA126556FTLc.-164C>A (n.-164C>A)
c.347C>A (p.Ser116Ter)
ClinVar dbSNP gnomAD v4
19g.48965344C=CA2340161164FTLc.-164C= (n.-164C=)
c.347C= (p.Ser116=)
19g.48965344C>GCA2695228967FTLc.-164C>G (n.-164C>G)
c.347C>G (p.Ser116Ter)
19g.48965344C>TCA149685FTLc.-164C>T (n.-164C>T)
c.347C>T (p.Ser116Leu)
ClinVar dbSNP gnomAD v4

Number of alleles fetched