Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.73323037A>CCA393086309HCN4c.3056T>G (p.Phe1019Cys)
c.1838T>G (p.Phe613Cys)
15g.73323037A>GCA393086310HCN4c.3056T>C (p.Phe1019Ser)
c.1838T>C (p.Phe613Ser)
15g.73323037A>TCA393086311HCN4c.3056T>A (p.Phe1019Tyr)
c.1838T>A (p.Phe613Tyr)
15g.73323038A>CCA393086314HCN4c.3055T>G (p.Phe1019Val)
c.1837T>G (p.Phe613Val)
15g.73323038A>GCA393086315HCN4c.3055T>C (p.Phe1019Leu)
c.1837T>C (p.Phe613Leu)
 gnomAD v4
15g.73323038A>TCA393086317HCN4c.3055T>A (p.Phe1019Ile)
c.1837T>A (p.Phe613Ile)
15g.73323039G>ACA272663846HCN4c.3054C>T (p.Gly1018=)
c.1836C>T (p.Gly612=)
 dbSNP gnomAD v2
15g.73323039G>CCA491478349HCN4c.3054C>G (p.Gly1018=)
c.1836C>G (p.Gly612=)
15g.73323039G=CA2187187310HCN4c.3054C= (p.Gly1018=)
c.1836C= (p.Gly612=)
15g.73323039G>TCA491478350HCN4c.3054C>A (p.Gly1018=)
c.1836C>A (p.Gly612=)
 gnomAD v4
15g.73323040C>ACA393086319HCN4c.3053G>T (p.Gly1018Val)
c.1835G>T (p.Gly612Val)
 gnomAD v4
15g.73323040C>GCA393086321HCN4c.3053G>C (p.Gly1018Ala)
c.1835G>C (p.Gly612Ala)
15g.73323040C>TCA393086322HCN4c.3053G>A (p.Gly1018Asp)
c.1835G>A (p.Gly612Asp)
15g.73323041C>ACA393086328HCN4c.3052G>T (p.Gly1018Cys)
c.1834G>T (p.Gly612Cys)
15g.73323041C>GCA393086325HCN4c.3052G>C (p.Gly1018Arg)
c.1834G>C (p.Gly612Arg)
15g.73323041C>TCA393086326HCN4c.3052G>A (p.Gly1018Ser)
c.1834G>A (p.Gly612Ser)
15g.73323042T>ACA491478359HCN4c.3051A>T (p.Val1017=)
c.1833A>T (p.Val611=)
15g.73323042T>CCA491478361HCN4c.3051A>G (p.Val1017=)
c.1833A>G (p.Val611=)
15g.73323042T>GCA491478362HCN4c.3051A>C (p.Val1017=)
c.1833A>C (p.Val611=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73323042T=CA2187187313HCN4c.3051A= (p.Val1017=)
c.1833A= (p.Val611=)
15g.73323043A=CA2187187316HCN4c.3050T= (p.Val1017=)
c.1832T= (p.Val611=)
15g.73323043A>CCA393086329HCN4c.3050T>G (p.Val1017Gly)
c.1832T>G (p.Val611Gly)
15g.73323043A>GCA393086331HCN4c.3050T>C (p.Val1017Ala)
c.1832T>C (p.Val611Ala)
15g.73323043A>TCA272663851HCN4c.3050T>A (p.Val1017Glu)
c.1832T>A (p.Val611Glu)
 dbSNP gnomAD v3 gnomAD v4
15g.73323044C>ACA393086334HCN4c.3049G>T (p.Val1017Leu)
c.1831G>T (p.Val611Leu)
 gnomAD v4
15g.73323044C=CA2187187318HCN4c.3049G= (p.Val1017=)
c.1831G= (p.Val611=)
15g.73323044C>GCA393086336HCN4c.3049G>C (p.Val1017Leu)
c.1831G>C (p.Val611Leu)
15g.73323044C>TCA393086337HCN4c.3049G>A (p.Val1017Ile)
c.1831G>A (p.Val611Ile)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73323045A>CCA491478368HCN4c.3048T>G (p.Pro1016=)
c.1830T>G (p.Pro610=)
15g.73323045A>GCA491478369HCN4c.3048T>C (p.Pro1016=)
c.1830T>C (p.Pro610=)
 gnomAD v4 COSMIC
15g.73323045A>TCA491478370HCN4c.3048T>A (p.Pro1016=)
c.1830T>A (p.Pro610=)
15g.73323046G>ACA7648893HCN4c.3047C>T (p.Pro1016Leu)
c.1829C>T (p.Pro610Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323046G>CCA393086339HCN4c.3047C>G (p.Pro1016Arg)
c.1829C>G (p.Pro610Arg)
15g.73323046G=CA2187187323HCN4c.3047C= (p.Pro1016=)
c.1829C= (p.Pro610=)
15g.73323046G>TCA393086341HCN4c.3047C>A (p.Pro1016His)
c.1829C>A (p.Pro610His)
 dbSNP gnomAD v2 gnomAD v4
15g.73323049delCA2575783829HCN4c.3047del (p.Pro1016LeufsTer2)
c.1829del (p.Pro610LeufsTer2)
 gnomAD v4
15g.73323047G>ACA393086343HCN4c.3046C>T (p.Pro1016Ser)
c.1828C>T (p.Pro610Ser)
15g.73323047G>CCA393086345HCN4c.3046C>G (p.Pro1016Ala)
c.1828C>G (p.Pro610Ala)
15g.73323047G>TCA393086346HCN4c.3046C>A (p.Pro1016Thr)
c.1828C>A (p.Pro610Thr)
 gnomAD v4
15g.73323048G>ACA7648894HCN4c.3045C>T (p.Ser1015=)
c.1827C>T (p.Ser609=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323048G>CCA491478374HCN4c.3045C>G (p.Ser1015=)
c.1827C>G (p.Ser609=)
15g.73323048G=CA2187187333HCN4c.3045C= (p.Ser1015=)
c.1827C= (p.Ser609=)
15g.73323048G>TCA491478376HCN4c.3045C>A (p.Ser1015=)
c.1827C>A (p.Ser609=)
 gnomAD v4
15g.73323049G>ACA393086350HCN4c.3044C>T (p.Ser1015Phe)
c.1826C>T (p.Ser609Phe)
 dbSNP gnomAD v2 gnomAD v4
15g.73323049G>CCA7648895HCN4c.3044C>G (p.Ser1015Cys)
c.1826C>G (p.Ser609Cys)
 ClinVar dbSNP ExAC gnomAD v4
15g.73323049G=CA2187187337HCN4c.3044C= (p.Ser1015=)
c.1826C= (p.Ser609=)
15g.73323049G>TCA393086348HCN4c.3044C>A (p.Ser1015Tyr)
c.1826C>A (p.Ser609Tyr)
 gnomAD v4
15g.73323050A>CCA393086353HCN4c.3043T>G (p.Ser1015Ala)
c.1825T>G (p.Ser609Ala)
15g.73323050A>GCA393086354HCN4c.3043T>C (p.Ser1015Pro)
c.1825T>C (p.Ser609Pro)
 gnomAD v4
15g.73323050A>TCA393086355HCN4c.3043T>A (p.Ser1015Thr)
c.1825T>A (p.Ser609Thr)
15g.73323051delCA2629370544HCN4c.3043del (p.Ser1015ProfsTer3)
c.1825del (p.Ser609ProfsTer3)
 gnomAD v4
15g.73323051A=CA2187187341HCN4c.3042T= (p.Ala1014=)
c.1824T= (p.Ala608=)
15g.73323051A>CCA491478386HCN4c.3042T>G (p.Ala1014=)
c.1824T>G (p.Ala608=)
15g.73323051A>GCA491478382HCN4c.3042T>C (p.Ala1014=)
c.1824T>C (p.Ala608=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73323051A>TCA491478383HCN4c.3042T>A (p.Ala1014=)
c.1824T>A (p.Ala608=)
15g.73323052G>ACA393086357HCN4c.3041C>T (p.Ala1014Val)
c.1823C>T (p.Ala608Val)
 gnomAD v4
15g.73323052G>CCA393086359HCN4c.3041C>G (p.Ala1014Gly)
c.1823C>G (p.Ala608Gly)
 ClinVar dbSNP gnomAD v4
15g.73323052G=CA2187187343HCN4c.3041C= (p.Ala1014=)
c.1823C= (p.Ala608=)
15g.73323052G>TCA393086361HCN4c.3041C>A (p.Ala1014Asp)
c.1823C>A (p.Ala608Asp)
 gnomAD v4
15g.73323053C>ACA393086364HCN4c.3040G>T (p.Ala1014Ser)
c.1822G>T (p.Ala608Ser)
 gnomAD v4
15g.73323053C>GCA393086365HCN4c.3040G>C (p.Ala1014Pro)
c.1822G>C (p.Ala608Pro)
15g.73323053C>TCA393086366HCN4c.3040G>A (p.Ala1014Thr)
c.1822G>A (p.Ala608Thr)
 gnomAD v4
15g.73323059dupCA7648896HCN4c.3040dup (p.Ala1014GlyfsTer?)
c.1822dup (p.Ala608GlyfsTer?)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.73323058_73323059dupCA2804714151HCN4c.3039_3040dup (p.Ala1014GlyfsTer5)
c.1821_1822dup (p.Ala608GlyfsTer5)
15g.73323059delCA645586808HCN4c.3040del (p.Ala1014LeufsTer4)
c.1822del (p.Ala608LeufsTer4)
 gnomAD v4 COSMIC
15g.73323054C>ACA491478397HCN4c.3039G>T (p.Gly1013=)
c.1821G>T (p.Gly607=)
 gnomAD v4
15g.73323054C=CA2187187352HCN4c.3039G= (p.Gly1013=)
c.1821G= (p.Gly607=)
15g.73323054C>GCA491478399HCN4c.3039G>C (p.Gly1013=)
c.1821G>C (p.Gly607=)
15g.73323054C>TCA491478402HCN4c.3039G>A (p.Gly1013=)
c.1821G>A (p.Gly607=)
 dbSNP gnomAD v2
15g.73323055C>ACA393086368HCN4c.3038G>T (p.Gly1013Val)
c.1820G>T (p.Gly607Val)
15g.73323055C>GCA393086370HCN4c.3038G>C (p.Gly1013Ala)
c.1820G>C (p.Gly607Ala)
 dbSNP
15g.73323055C>TCA393086371HCN4c.3038G>A (p.Gly1013Glu)
c.1820G>A (p.Gly607Glu)
 gnomAD v4 COSMIC
15g.73323056C>ACA393086377HCN4c.3037G>T (p.Gly1013Trp)
c.1819G>T (p.Gly607Trp)
15g.73323056C>GCA393086375HCN4c.3037G>C (p.Gly1013Arg)
c.1819G>C (p.Gly607Arg)
15g.73323056C>TCA393086373HCN4c.3037G>A (p.Gly1013Arg)
c.1819G>A (p.Gly607Arg)
15g.73323057C>ACA491478408HCN4c.3036G>T (p.Gly1012=)
c.1818G>T (p.Gly606=)
 gnomAD v4
15g.73323057C=CA2187187356HCN4c.3036G= (p.Gly1012=)
c.1818G= (p.Gly606=)
15g.73323057C>GCA272663905HCN4c.3036G>C (p.Gly1012=)
c.1818G>C (p.Gly606=)
 ClinVar dbSNP gnomAD v4
15g.73323057C>TCA491478411HCN4c.3036G>A (p.Gly1012=)
c.1818G>A (p.Gly606=)
 gnomAD v4
15g.73323058C>ACA393086378HCN4c.3035G>T (p.Gly1012Val)
c.1817G>T (p.Gly606Val)
 gnomAD v4
15g.73323058C=CA2187187361HCN4c.3035G= (p.Gly1012=)
c.1817G= (p.Gly606=)
15g.73323058C>GCA7648897HCN4c.3035G>C (p.Gly1012Ala)
c.1817G>C (p.Gly606Ala)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.73323058C>TCA393086380HCN4c.3035G>A (p.Gly1012Glu)
c.1817G>A (p.Gly606Glu)
 gnomAD v4
15g.73323059C>ACA7648898HCN4c.3034G>T (p.Gly1012Trp)
c.1816G>T (p.Gly606Trp)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.73323059C=CA2187187364HCN4c.3034G= (p.Gly1012=)
c.1816G= (p.Gly606=)
15g.73323059C>GCA393086382HCN4c.3034G>C (p.Gly1012Arg)
c.1816G>C (p.Gly606Arg)
 dbSNP gnomAD v4
15g.73323059C>TCA7648899HCN4c.3034G>A (p.Gly1012Arg)
c.1816G>A (p.Gly606Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.73323060A=CA2187187372HCN4c.3033T= (p.Ser1011=)
c.1815T= (p.Ser605=)
15g.73323060A>CCA199745HCN4c.3033T>G (p.Ser1011=)
c.1815T>G (p.Ser605=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323060A>GCA491478417HCN4c.3033T>C (p.Ser1011=)
c.1815T>C (p.Ser605=)
 gnomAD v4
15g.73323060A>TCA491478418HCN4c.3033T>A (p.Ser1011=)
c.1815T>A (p.Ser605=)
15g.73323061G>ACA393086385HCN4c.3032C>T (p.Ser1011Phe)
c.1814C>T (p.Ser605Phe)
 gnomAD v4
15g.73323061G>CCA393086387HCN4c.3032C>G (p.Ser1011Cys)
c.1814C>G (p.Ser605Cys)
15g.73323061G>TCA393086389HCN4c.3032C>A (p.Ser1011Tyr)
c.1814C>A (p.Ser605Tyr)
 gnomAD v4
15g.73323062A=CA2187187378HCN4c.3031T= (p.Ser1011=)
c.1813T= (p.Ser605=)
15g.73323062A>CCA393086391HCN4c.3031T>G (p.Ser1011Ala)
c.1813T>G (p.Ser605Ala)
 gnomAD v4
15g.73323062A>GCA16607866HCN4c.3031T>C (p.Ser1011Pro)
c.1813T>C (p.Ser605Pro)
 ClinVar dbSNP gnomAD v3 gnomAD v4
15g.73323062A>TCA393086393HCN4c.3031T>A (p.Ser1011Thr)
c.1813T>A (p.Ser605Thr)
15g.73323063G>ACA7648900HCN4c.3030C>T (p.Ala1010=)
c.1812C>T (p.Ala604=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323063G>CCA491478426HCN4c.3030C>G (p.Ala1010=)
c.1812C>G (p.Ala604=)
15g.73323063G=CA2187187381HCN4c.3030C= (p.Ala1010=)
c.1812C= (p.Ala604=)
15g.73323063G>TCA491478425HCN4c.3030C>A (p.Ala1010=)
c.1812C>A (p.Ala604=)
 gnomAD v4
15g.73323064G>ACA393086397HCN4c.3029C>T (p.Ala1010Val)
c.1811C>T (p.Ala604Val)
 gnomAD v4
15g.73323064G>CCA393086399HCN4c.3029C>G (p.Ala1010Gly)
c.1811C>G (p.Ala604Gly)
 gnomAD v4
15g.73323064G=CA2187187384HCN4c.3029C= (p.Ala1010=)
c.1811C= (p.Ala604=)
15g.73323064G>TCA393086396HCN4c.3029C>A (p.Ala1010Asp)
c.1811C>A (p.Ala604Asp)
 gnomAD v4
15g.73323065C>ACA393086402HCN4c.3028G>T (p.Ala1010Ser)
c.1810G>T (p.Ala604Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73323065C=CA2187187391HCN4c.3028G= (p.Ala1010=)
c.1810G= (p.Ala604=)
15g.73323065C>GCA393086404HCN4c.3028G>C (p.Ala1010Pro)
c.1810G>C (p.Ala604Pro)
15g.73323065C>TCA7648901HCN4c.3028G>A (p.Ala1010Thr)
c.1810G>A (p.Ala604Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.73323068dupCA272663932HCN4c.3028dup (p.Ala1010GlyfsTer?)
c.1810dup (p.Ala604GlyfsTer?)
 dbSNP gnomAD v4
15g.73323068delCA2629370545HCN4c.3028del (p.Ala1010ProfsTer8)
c.1810del (p.Ala604ProfsTer8)
 gnomAD v4
15g.73323066C>ACA491478437HCN4c.3027G>T (p.Gly1009=)
c.1809G>T (p.Gly603=)
 gnomAD v4
15g.73323066C>GCA491478438HCN4c.3027G>C (p.Gly1009=)
c.1809G>C (p.Gly603=)
15g.73323066C>TCA491478440HCN4c.3027G>A (p.Gly1009=)
c.1809G>A (p.Gly603=)
15g.73323067C>ACA393086406HCN4c.3026G>T (p.Gly1009Val)
c.1808G>T (p.Gly603Val)
15g.73323067C=CA2187187397HCN4c.3026G= (p.Gly1009=)
c.1808G= (p.Gly603=)
15g.73323067C>GCA393086407HCN4c.3026G>C (p.Gly1009Ala)
c.1808G>C (p.Gly603Ala)
15g.73323067C>TCA7648902HCN4c.3026G>A (p.Gly1009Glu)
c.1808G>A (p.Gly603Glu)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.73323068C>ACA393086410HCN4c.3025G>T (p.Gly1009Trp)
c.1807G>T (p.Gly603Trp)
15g.73323068C>GCA393086411HCN4c.3025G>C (p.Gly1009Arg)
c.1807G>C (p.Gly603Arg)
 gnomAD v4
15g.73323068C>TCA393086413HCN4c.3025G>A (p.Gly1009Arg)
c.1807G>A (p.Gly603Arg)
 gnomAD v4
15g.73323069T>ACA491478447HCN4c.3024A>T (p.Ala1008=)
c.1806A>T (p.Ala602=)
15g.73323069T>CCA491478448HCN4c.3024A>G (p.Ala1008=)
c.1806A>G (p.Ala602=)
 gnomAD v4
15g.73323069T>GCA491478449HCN4c.3024A>C (p.Ala1008=)
c.1806A>C (p.Ala602=)
15g.73323070G>ACA393086415HCN4c.3023C>T (p.Ala1008Val)
c.1805C>T (p.Ala602Val)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73323070G>CCA393086417HCN4c.3023C>G (p.Ala1008Gly)
c.1805C>G (p.Ala602Gly)
15g.73323070G=CA2187187400HCN4c.3023C= (p.Ala1008=)
c.1805C= (p.Ala602=)
15g.73323070G>TCA393086419HCN4c.3023C>A (p.Ala1008Glu)
c.1805C>A (p.Ala602Glu)
 gnomAD v4
15g.73323071C>ACA393086424HCN4c.3022G>T (p.Ala1008Ser)
c.1804G>T (p.Ala602Ser)
 ClinVar dbSNP gnomAD v4
15g.73323071C=CA2187187403HCN4c.3022G= (p.Ala1008=)
c.1804G= (p.Ala602=)
15g.73323071C>GCA393086420HCN4c.3022G>C (p.Ala1008Pro)
c.1804G>C (p.Ala602Pro)
15g.73323071C>TCA393086422HCN4c.3022G>A (p.Ala1008Thr)
c.1804G>A (p.Ala602Thr)
 gnomAD v4
15g.73323072C>ACA491478456HCN4c.3021G>T (p.Val1007=)
c.1803G>T (p.Val601=)
 gnomAD v4
15g.73323072C=CA2187187406HCN4c.3021G= (p.Val1007=)
c.1803G= (p.Val601=)
15g.73323072C>GCA491478454HCN4c.3021G>C (p.Val1007=)
c.1803G>C (p.Val601=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
15g.73323072C>TCA491478452HCN4c.3021G>A (p.Val1007=)
c.1803G>A (p.Val601=)
 ClinVar dbSNP gnomAD v4
15g.73323072_73323079delinsCACAAGGGCA2187187408HCN4c.3014_3021delinsCCCTTGTG (p.Ser1005=)
c.1796_1803delinsCCCTTGTG (p.Ser599=)
15g.73323073A>CCA393086426HCN4c.3020T>G (p.Val1007Gly)
c.1802T>G (p.Val601Gly)
 gnomAD v4
15g.73323073A>GCA393086427HCN4c.3020T>C (p.Val1007Ala)
c.1802T>C (p.Val601Ala)
 ClinVar gnomAD v4
15g.73323073A>TCA393086429HCN4c.3020T>A (p.Val1007Glu)
c.1802T>A (p.Val601Glu)
15g.73323075_73323081delCA971394547HCN4c.3014_3020del (p.Ser1005TrpfsTer11)
c.1796_1802del (p.Ser599TrpfsTer11)
 dbSNP gnomAD v3 gnomAD v4
15g.73323074C>ACA272663938HCN4c.3019G>T (p.Val1007Leu)
c.1801G>T (p.Val601Leu)
 dbSNP gnomAD v4
15g.73323074C=CA2187187417HCN4c.3019G= (p.Val1007=)
c.1801G= (p.Val601=)
15g.73323074C>GCA393086431HCN4c.3019G>C (p.Val1007Leu)
c.1801G>C (p.Val601Leu)
15g.73323074C>TCA393086432HCN4c.3019G>A (p.Val1007Met)
c.1801G>A (p.Val601Met)
 ClinVar dbSNP gnomAD v4
15g.73323075A>CCA491478462HCN4c.3018T>G (p.Leu1006=)
c.1800T>G (p.Leu600=)
15g.73323075A>GCA491478463HCN4c.3018T>C (p.Leu1006=)
c.1800T>C (p.Leu600=)
 gnomAD v4
15g.73323075A>TCA491478465HCN4c.3018T>A (p.Leu1006=)
c.1800T>A (p.Leu600=)
15g.73323076A=CA2187187422HCN4c.3017T= (p.Leu1006=)
c.1799T= (p.Leu600=)
15g.73323076A>CCA393086434HCN4c.3017T>G (p.Leu1006Arg)
c.1799T>G (p.Leu600Arg)
15g.73323076A>GCA393086436HCN4c.3017T>C (p.Leu1006Pro)
c.1799T>C (p.Leu600Pro)
 ClinVar dbSNP gnomAD v4
15g.73323076A>TCA393086438HCN4c.3017T>A (p.Leu1006His)
c.1799T>A (p.Leu600His)
15g.73323077G>ACA393086439HCN4c.3016C>T (p.Leu1006Phe)
c.1798C>T (p.Leu600Phe)
 gnomAD v4
15g.73323077G>CCA393086440HCN4c.3016C>G (p.Leu1006Val)
c.1798C>G (p.Leu600Val)
15g.73323077G>TCA393086442HCN4c.3016C>A (p.Leu1006Ile)
c.1798C>A (p.Leu600Ile)
 gnomAD v4
15g.73323078G>ACA491478469HCN4c.3015C>T (p.Ser1005=)
c.1797C>T (p.Ser599=)
 dbSNP gnomAD v2 gnomAD v4
15g.73323078G>CCA491478472HCN4c.3015C>G (p.Ser1005=)
c.1797C>G (p.Ser599=)
15g.73323078G=CA2187187426HCN4c.3015C= (p.Ser1005=)
c.1797C= (p.Ser599=)
15g.73323078G>TCA491478473HCN4c.3015C>A (p.Ser1005=)
c.1797C>A (p.Ser599=)
 gnomAD v4
15g.73323079G>ACA7648903HCN4c.3014C>T (p.Ser1005Phe)
c.1796C>T (p.Ser599Phe)
 ClinVar dbSNP ExAC gnomAD v4
15g.73323079G>CCA393086446HCN4c.3014C>G (p.Ser1005Cys)
c.1796C>G (p.Ser599Cys)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73323079G=CA2187187433HCN4c.3014C= (p.Ser1005=)
c.1796C= (p.Ser599=)
15g.73323079G>TCA393086445HCN4c.3014C>A (p.Ser1005Tyr)
c.1796C>A (p.Ser599Tyr)
 gnomAD v4
15g.73323080A>CCA393086448HCN4c.3013T>G (p.Ser1005Ala)
c.1795T>G (p.Ser599Ala)
15g.73323080A>GCA393086451HCN4c.3013T>C (p.Ser1005Pro)
c.1795T>C (p.Ser599Pro)
 gnomAD v4
15g.73323080A>TCA393086450HCN4c.3013T>A (p.Ser1005Thr)
c.1795T>A (p.Ser599Thr)
15g.73323081C>ACA491478480HCN4c.3012G>T (p.Pro1004=)
c.1794G>T (p.Pro598=)
 gnomAD v4
15g.73323081C=CA2187187439HCN4c.3012G= (p.Pro1004=)
c.1794G= (p.Pro598=)
15g.73323081C>GCA272663947HCN4c.3012G>C (p.Pro1004=)
c.1794G>C (p.Pro598=)
 dbSNP
15g.73323081C>TCA7648904HCN4c.3012G>A (p.Pro1004=)
c.1794G>A (p.Pro598=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323082G>ACA393086455HCN4c.3011C>T (p.Pro1004Leu)
c.1793C>T (p.Pro598Leu)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73323082G>CCA393086454HCN4c.3011C>G (p.Pro1004Arg)
c.1793C>G (p.Pro598Arg)
 gnomAD v4
15g.73323082G=CA2187187444HCN4c.3011C= (p.Pro1004=)
c.1793C= (p.Pro598=)
15g.73323082G>TCA393086457HCN4c.3011C>A (p.Pro1004Gln)
c.1793C>A (p.Pro598Gln)
 gnomAD v4
15g.73323083delCA2499223089HCN4c.3011del (p.Pro1004ArgfsTer14)
c.1793del (p.Pro598ArgfsTer14)
 ClinVar dbSNP
15g.73323083G>ACA7648905HCN4c.3010C>T (p.Pro1004Ser)
c.1792C>T (p.Pro598Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323083G>CCA393086458HCN4c.3010C>G (p.Pro1004Ala)
c.1792C>G (p.Pro598Ala)
15g.73323083G=CA2187187448HCN4c.3010C= (p.Pro1004=)
c.1792C= (p.Pro598=)
15g.73323083G>TCA393086460HCN4c.3010C>A (p.Pro1004Thr)
c.1792C>A (p.Pro598Thr)
15g.73323084C>ACA491478491HCN4c.3009G>T (p.Pro1003=)
c.1791G>T (p.Pro597=)
 gnomAD v4
15g.73323084C=CA2187187456HCN4c.3009G= (p.Pro1003=)
c.1791G= (p.Pro597=)
15g.73323084C>GCA491478492HCN4c.3009G>C (p.Pro1003=)
c.1791G>C (p.Pro597=)
15g.73323084C>TCA7648906HCN4c.3009G>A (p.Pro1003=)
c.1791G>A (p.Pro597=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
15g.73323085G>ACA393086462HCN4c.3008C>T (p.Pro1003Leu)
c.1790C>T (p.Pro597Leu)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73323085G>CCA393086464HCN4c.3008C>G (p.Pro1003Arg)
c.1790C>G (p.Pro597Arg)
15g.73323085G=CA2187187458HCN4c.3008C= (p.Pro1003=)
c.1790C= (p.Pro597=)
15g.73323085G>TCA393086466HCN4c.3008C>A (p.Pro1003Gln)
c.1790C>A (p.Pro597Gln)
 gnomAD v4
15g.73323086G>ACA393086467HCN4c.3007C>T (p.Pro1003Ser)
c.1789C>T (p.Pro597Ser)
 gnomAD v4
15g.73323086G>CCA393086469HCN4c.3007C>G (p.Pro1003Ala)
c.1789C>G (p.Pro597Ala)
15g.73323086G>TCA393086471HCN4c.3007C>A (p.Pro1003Thr)
c.1789C>A (p.Pro597Thr)
 gnomAD v4
15g.73323087C>ACA393086473HCN4c.3006G>T (p.Glu1002Asp)
c.1788G>T (p.Glu596Asp)
 gnomAD v4
15g.73323087C>GCA393086474HCN4c.3006G>C (p.Glu1002Asp)
c.1788G>C (p.Glu596Asp)
15g.73323087C>TCA491478498HCN4c.3006G>A (p.Glu1002=)
c.1788G>A (p.Glu596=)
15g.73323088T>ACA393086479HCN4c.3005A>T (p.Glu1002Val)
c.1787A>T (p.Glu596Val)
15g.73323088T>CCA393086477HCN4c.3005A>G (p.Glu1002Gly)
c.1787A>G (p.Glu596Gly)
 gnomAD v4
15g.73323088T>GCA393086478HCN4c.3005A>C (p.Glu1002Ala)
c.1787A>C (p.Glu596Ala)
15g.73323089C>ACA393086481HCN4c.3004G>T (p.Glu1002Ter)
c.1786G>T (p.Glu596Ter)
 gnomAD v4
15g.73323089C=CA2187187464HCN4c.3004G= (p.Glu1002=)
c.1786G= (p.Glu596=)
15g.73323089C>GCA16614917HCN4c.3004G>C (p.Glu1002Gln)
c.1786G>C (p.Glu596Gln)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73323089C>TCA393086483HCN4c.3004G>A (p.Glu1002Lys)
c.1786G>A (p.Glu596Lys)
 ClinVar dbSNP gnomAD v4
15g.73323090A>CCA491478503HCN4c.3003T>G (p.Pro1001=)
c.1785T>G (p.Pro595=)
15g.73323090A>GCA491478504HCN4c.3003T>C (p.Pro1001=)
c.1785T>C (p.Pro595=)
 gnomAD v4
15g.73323090A>TCA491478505HCN4c.3003T>A (p.Pro1001=)
c.1785T>A (p.Pro595=)
 gnomAD v4
15g.73323091G>ACA393086485HCN4c.3002C>T (p.Pro1001Leu)
c.1784C>T (p.Pro595Leu)
15g.73323091G>CCA393086486HCN4c.3002C>G (p.Pro1001Arg)
c.1784C>G (p.Pro595Arg)
15g.73323091G=CA2187187469HCN4c.3002C= (p.Pro1001=)
c.1784C= (p.Pro595=)
15g.73323091G>TCA272663955HCN4c.3002C>A (p.Pro1001His)
c.1784C>A (p.Pro595His)
 dbSNP gnomAD v4
15g.73323092G>ACA393086489HCN4c.3001C>T (p.Pro1001Ser)
c.1783C>T (p.Pro595Ser)
 gnomAD v4
15g.73323092G>CCA393086491HCN4c.3001C>G (p.Pro1001Ala)
c.1783C>G (p.Pro595Ala)
15g.73323092G>TCA393086492HCN4c.3001C>A (p.Pro1001Thr)
c.1783C>A (p.Pro595Thr)
 ClinVar gnomAD v4
15g.73323093C>ACA393086494HCN4c.3000G>T (p.Gln1000His)
c.1782G>T (p.Gln594His)
 gnomAD v4
15g.73323093C>GCA393086495HCN4c.3000G>C (p.Gln1000His)
c.1782G>C (p.Gln594His)
15g.73323093C>TCA491478508HCN4c.3000G>A (p.Gln1000=)
c.1782G>A (p.Gln594=)
 gnomAD v4
15g.73323094T>ACA393086500HCN4c.2999A>T (p.Gln1000Leu)
c.1781A>T (p.Gln594Leu)
15g.73323094T>CCA393086499HCN4c.2999A>G (p.Gln1000Arg)
c.1781A>G (p.Gln594Arg)
15g.73323094T>GCA393086497HCN4c.2999A>C (p.Gln1000Pro)
c.1781A>C (p.Gln594Pro)
15g.73323095G>ACA393086502HCN4c.2998C>T (p.Gln1000Ter)
c.1780C>T (p.Gln594Ter)
 gnomAD v4
15g.73323095G>CCA393086504HCN4c.2998C>G (p.Gln1000Glu)
c.1780C>G (p.Gln594Glu)
15g.73323095G=CA2187187474HCN4c.2998C= (p.Gln1000=)
c.1780C= (p.Gln594=)
15g.73323095G>TCA393086506HCN4c.2998C>A (p.Gln1000Lys)
c.1780C>A (p.Gln594Lys)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73323096C>ACA491478517HCN4c.2997G>T (p.Arg999=)
c.1779G>T (p.Arg593=)
 gnomAD v4
15g.73323096C=CA2187187481HCN4c.2997G= (p.Arg999=)
c.1779G= (p.Arg593=)
15g.73323096C>GCA7648907HCN4c.2997G>C (p.Arg999=)
c.1779G>C (p.Arg593=)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.73323096C>TCA7648908HCN4c.2997G>A (p.Arg999=)
c.1779G>A (p.Arg593=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323097C>ACA393086514HCN4c.2996G>T (p.Arg999Leu)
c.1778G>T (p.Arg593Leu)
 gnomAD v4
15g.73323097C=CA2187187487HCN4c.2996G= (p.Arg999=)
c.1778G= (p.Arg593=)
15g.73323097C>GCA393086516HCN4c.2996G>C (p.Arg999Pro)
c.1778G>C (p.Arg593Pro)
15g.73323097C>TCA393086517HCN4c.2996G>A (p.Arg999Gln)
c.1778G>A (p.Arg593Gln)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73323098G>ACA272663979HCN4c.2995C>T (p.Arg999Trp)
c.1777C>T (p.Arg593Trp)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
15g.73323098G>CCA393086522HCN4c.2995C>G (p.Arg999Gly)
c.1777C>G (p.Arg593Gly)
15g.73323098G=CA2187187494HCN4c.2995C= (p.Arg999=)
c.1777C= (p.Arg593=)
15g.73323098G>TCA491478524HCN4c.2995C>A (p.Arg999=)
c.1777C>A (p.Arg593=)
 gnomAD v4
15g.73323099T>ACA491478526HCN4c.2994A>T (p.Pro998=)
c.1776A>T (p.Pro592=)
15g.73323099T>CCA491478527HCN4c.2994A>G (p.Pro998=)
c.1776A>G (p.Pro592=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73323099T>GCA491478528HCN4c.2994A>C (p.Pro998=)
c.1776A>C (p.Pro592=)
15g.73323099T=CA2187187499HCN4c.2994A= (p.Pro998=)
c.1776A= (p.Pro592=)
15g.73323100G>ACA7648909HCN4c.2993C>T (p.Pro998Leu)
c.1775C>T (p.Pro592Leu)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.73323100G>CCA393086525HCN4c.2993C>G (p.Pro998Arg)
c.1775C>G (p.Pro592Arg)
15g.73323100G=CA2187187502HCN4c.2993C= (p.Pro998=)
c.1775C= (p.Pro592=)
15g.73323100G>TCA393086528HCN4c.2993C>A (p.Pro998Gln)
c.1775C>A (p.Pro592Gln)
 gnomAD v4
15g.73323104delCA491478535HCN4c.2993del (p.Pro998HisfsTer20)
c.1775del (p.Pro592HisfsTer20)
 gnomAD v4 COSMIC
15g.73323101G>ACA393086536HCN4c.2992C>T (p.Pro998Ser)
c.1774C>T (p.Pro592Ser)
 gnomAD v4
15g.73323101G>CCA7648910HCN4c.2992C>G (p.Pro998Ala)
c.1774C>G (p.Pro592Ala)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.73323101G=CA2187187504HCN4c.2992C= (p.Pro998=)
c.1774C= (p.Pro592=)
15g.73323101G>TCA393086534HCN4c.2992C>A (p.Pro998Thr)
c.1774C>A (p.Pro592Thr)
 gnomAD v4
15g.73323102G>ACA491478537HCN4c.2991C>T (p.Pro997=)
c.1773C>T (p.Pro591=)
 dbSNP gnomAD v2 gnomAD v4
15g.73323102G>CCA491478539HCN4c.2991C>G (p.Pro997=)
c.1773C>G (p.Pro591=)
 gnomAD v4
15g.73323102G=CA2187187506HCN4c.2991C= (p.Pro997=)
c.1773C= (p.Pro591=)
15g.73323102G>TCA491478540HCN4c.2991C>A (p.Pro997=)
c.1773C>A (p.Pro591=)
15g.73323103G>ACA393086539HCN4c.2990C>T (p.Pro997Leu)
c.1772C>T (p.Pro591Leu)
 gnomAD v4
15g.73323103G>CCA393086541HCN4c.2990C>G (p.Pro997Arg)
c.1772C>G (p.Pro591Arg)
15g.73323103G=CA2187187511HCN4c.2990C= (p.Pro997=)
c.1772C= (p.Pro591=)
15g.73323103G>TCA272663982HCN4c.2990C>A (p.Pro997His)
c.1772C>A (p.Pro591His)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73323104G>ACA393086551HCN4c.2989C>T (p.Pro997Ser)
c.1771C>T (p.Pro591Ser)
 gnomAD v4
15g.73323104G>CCA393086554HCN4c.2989C>G (p.Pro997Ala)
c.1771C>G (p.Pro591Ala)
15g.73323104G=CA2187187516HCN4c.2989C= (p.Pro997=)
c.1771C= (p.Pro591=)
15g.73323104G>TCA7648911HCN4c.2989C>A (p.Pro997Thr)
c.1771C>A (p.Pro591Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.73323105T>ACA491478550HCN4c.2988A>T (p.Thr996=)
c.1770A>T (p.Thr590=)
 dbSNP
15g.73323105T>CCA491478551HCN4c.2988A>G (p.Thr996=)
c.1770A>G (p.Thr590=)
 gnomAD v4
15g.73323105T>GCA491478553HCN4c.2988A>C (p.Thr996=)
c.1770A>C (p.Thr590=)
 ClinVar
15g.73323105T=CA2187187520HCN4c.2988A= (p.Thr996=)
c.1770A= (p.Thr590=)
15g.73323106G>ACA393086559HCN4c.2987C>T (p.Thr996Ile)
c.1769C>T (p.Thr590Ile)
 gnomAD v4
15g.73323106G>CCA393086561HCN4c.2987C>G (p.Thr996Arg)
c.1769C>G (p.Thr590Arg)
15g.73323106G>TCA393086563HCN4c.2987C>A (p.Thr996Lys)
c.1769C>A (p.Thr590Lys)
 gnomAD v4
15g.73323107T>ACA393086567HCN4c.2986A>T (p.Thr996Ser)
c.1768A>T (p.Thr590Ser)
 dbSNP
15g.73323107T>CCA393086568HCN4c.2986A>G (p.Thr996Ala)
c.1768A>G (p.Thr590Ala)
 gnomAD v4
15g.73323107T>GCA393086570HCN4c.2986A>C (p.Thr996Pro)
c.1768A>C (p.Thr590Pro)
15g.73323107T=CA2187187523HCN4c.2986A= (p.Thr996=)
c.1768A= (p.Thr590=)
15g.73323108C>ACA393086573HCN4c.2985G>T (p.Glu995Asp)
c.1767G>T (p.Glu589Asp)
 gnomAD v4
15g.73323108C>GCA393086575HCN4c.2985G>C (p.Glu995Asp)
c.1767G>C (p.Glu589Asp)
 ClinVar gnomAD v4
15g.73323108C>TCA491478563HCN4c.2985G>A (p.Glu995=)
c.1767G>A (p.Glu589=)
 gnomAD v4
15g.73323109T>ACA393086579HCN4c.2984A>T (p.Glu995Val)
c.1766A>T (p.Glu589Val)
15g.73323109T>CCA393086583HCN4c.2984A>G (p.Glu995Gly)
c.1766A>G (p.Glu589Gly)
 gnomAD v4
15g.73323109T>GCA393086581HCN4c.2984A>C (p.Glu995Ala)
c.1766A>C (p.Glu589Ala)
15g.73323110C>ACA393086587HCN4c.2983G>T (p.Glu995Ter)
c.1765G>T (p.Glu589Ter)
 gnomAD v4
15g.73323110C>GCA393086590HCN4c.2983G>C (p.Glu995Gln)
c.1765G>C (p.Glu589Gln)
15g.73323110C>TCA393086591HCN4c.2983G>A (p.Glu995Lys)
c.1765G>A (p.Glu589Lys)
15g.73323111T>ACA491478567HCN4c.2982A>T (p.Pro994=)
c.1764A>T (p.Pro588=)
15g.73323111T>CCA491478570HCN4c.2982A>G (p.Pro994=)
c.1764A>G (p.Pro588=)
 dbSNP
15g.73323111T>GCA491478573HCN4c.2982A>C (p.Pro994=)
c.1764A>C (p.Pro588=)
15g.73323111T=CA2187187525HCN4c.2982A= (p.Pro994=)
c.1764A= (p.Pro588=)
15g.73323112G>ACA393086595HCN4c.2981C>T (p.Pro994Leu)
c.1763C>T (p.Pro588Leu)
 gnomAD v4
15g.73323112G>CCA393086597HCN4c.2981C>G (p.Pro994Arg)
c.1763C>G (p.Pro588Arg)
15g.73323112G>TCA393086599HCN4c.2981C>A (p.Pro994Gln)
c.1763C>A (p.Pro588Gln)
 gnomAD v4
15g.73323113G>ACA393086602HCN4c.2980C>T (p.Pro994Ser)
c.1762C>T (p.Pro588Ser)
 gnomAD v4
15g.73323113G>CCA393086603HCN4c.2980C>G (p.Pro994Ala)
c.1762C>G (p.Pro588Ala)
15g.73323113G>TCA393086606HCN4c.2980C>A (p.Pro994Thr)
c.1762C>A (p.Pro588Thr)
15g.73323114C>ACA491478585HCN4c.2979G>T (p.Thr993=)
c.1761G>T (p.Thr587=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
15g.73323114C=CA2187187528HCN4c.2979G= (p.Thr993=)
c.1761G= (p.Thr587=)
15g.73323114C>GCA491478584HCN4c.2979G>C (p.Thr993=)
c.1761G>C (p.Thr587=)
 ClinVar
15g.73323114C>TCA203637HCN4c.2979G>A (p.Thr993=)
c.1761G>A (p.Thr587=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323115G>ACA7648912HCN4c.2978C>T (p.Thr993Met)
c.1760C>T (p.Thr587Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323115G>CCA393086610HCN4c.2978C>G (p.Thr993Arg)
c.1760C>G (p.Thr587Arg)
 gnomAD v4
15g.73323115G=CA2187187536HCN4c.2978C= (p.Thr993=)
c.1760C= (p.Thr587=)
15g.73323115G>TCA393086609HCN4c.2978C>A (p.Thr993Lys)
c.1760C>A (p.Thr587Lys)
 COSMIC
15g.73323116T>ACA393086614HCN4c.2977A>T (p.Thr993Ser)
c.1759A>T (p.Thr587Ser)
 dbSNP
15g.73323116T>CCA393086615HCN4c.2977A>G (p.Thr993Ala)
c.1759A>G (p.Thr587Ala)
 gnomAD v4
15g.73323116T>GCA393086617HCN4c.2977A>C (p.Thr993Pro)
c.1759A>C (p.Thr587Pro)
15g.73323116T=CA2187187541HCN4c.2977A= (p.Thr993=)
c.1759A= (p.Thr587=)
15g.73323117G>ACA7648913HCN4c.2976C>T (p.Ser992=)
c.1758C>T (p.Ser586=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.73323117G>CCA393086619HCN4c.2976C>G (p.Ser992Arg)
c.1758C>G (p.Ser586Arg)
15g.73323117G=CA2187187543HCN4c.2976C= (p.Ser992=)
c.1758C= (p.Ser586=)
15g.73323117G>TCA393086620HCN4c.2976C>A (p.Ser992Arg)
c.1758C>A (p.Ser586Arg)
 gnomAD v4
15g.73323118C>ACA7648914HCN4c.2975G>T (p.Ser992Ile)
c.1757G>T (p.Ser586Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323118C=CA2187187548HCN4c.2975G= (p.Ser992=)
c.1757G= (p.Ser586=)
15g.73323118C>GCA393086622HCN4c.2975G>C (p.Ser992Thr)
c.1757G>C (p.Ser586Thr)
15g.73323118C>TCA393086623HCN4c.2975G>A (p.Ser992Asn)
c.1757G>A (p.Ser586Asn)
 gnomAD v4
15g.73323119T>ACA393086625HCN4c.2974A>T (p.Ser992Cys)
c.1756A>T (p.Ser586Cys)
15g.73323119T>CCA393086627HCN4c.2974A>G (p.Ser992Gly)
c.1756A>G (p.Ser586Gly)
 gnomAD v4
15g.73323119T>GCA393086628HCN4c.2974A>C (p.Ser992Arg)
c.1756A>C (p.Ser586Arg)
15g.73323120C>ACA491478598HCN4c.2973G>T (p.Leu991=)
c.1755G>T (p.Leu585=)
 gnomAD v4
15g.73323120C=CA2187187551HCN4c.2973G= (p.Leu991=)
c.1755G= (p.Leu585=)
15g.73323120C>GCA491478601HCN4c.2973G>C (p.Leu991=)
c.1755G>C (p.Leu585=)
15g.73323120C>TCA491478600HCN4c.2973G>A (p.Leu991=)
c.1755G>A (p.Leu585=)
 dbSNP
15g.73323121A=CA2187187553HCN4c.2972T= (p.Leu991=)
c.1754T= (p.Leu585=)
15g.73323121A>CCA393086631HCN4c.2972T>G (p.Leu991Arg)
c.1754T>G (p.Leu585Arg)
15g.73323121A>GCA272663993HCN4c.2972T>C (p.Leu991Pro)
c.1754T>C (p.Leu585Pro)
 dbSNP gnomAD v2 gnomAD v4
15g.73323121A>TCA393086629HCN4c.2972T>A (p.Leu991Gln)
c.1754T>A (p.Leu585Gln)
15g.73323122G>ACA491478607HCN4c.2971C>T (p.Leu991=)
c.1753C>T (p.Leu585=)
 gnomAD v4
15g.73323122G>CCA393086633HCN4c.2971C>G (p.Leu991Val)
c.1753C>G (p.Leu585Val)
15g.73323122G>TCA393086634HCN4c.2971C>A (p.Leu991Met)
c.1753C>A (p.Leu585Met)
 gnomAD v4 COSMIC
15g.73323123T>ACA491478609HCN4c.2970A>T (p.Pro990=)
c.1752A>T (p.Pro584=)
 gnomAD v4
15g.73323123T>CCA491478611HCN4c.2970A>G (p.Pro990=)
c.1752A>G (p.Pro584=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73323123T>GCA491478613HCN4c.2970A>C (p.Pro990=)
c.1752A>C (p.Pro584=)
15g.73323123T=CA2187187556HCN4c.2970A= (p.Pro990=)
c.1752A= (p.Pro584=)
15g.73323124G>ACA7648915HCN4c.2969C>T (p.Pro990Leu)
c.1751C>T (p.Pro584Leu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323124G>CCA393086637HCN4c.2969C>G (p.Pro990Arg)
c.1751C>G (p.Pro584Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73323124G=CA2187187559HCN4c.2969C= (p.Pro990=)
c.1751C= (p.Pro584=)
15g.73323124G>TCA393086639HCN4c.2969C>A (p.Pro990Gln)
c.1751C>A (p.Pro584Gln)
 gnomAD v4
15g.73323125G>ACA393086643HCN4c.2968C>T (p.Pro990Ser)
c.1750C>T (p.Pro584Ser)
 gnomAD v4
15g.73323125G>CCA393086642HCN4c.2968C>G (p.Pro990Ala)
c.1750C>G (p.Pro584Ala)
 ClinVar dbSNP
15g.73323125G>TCA393086640HCN4c.2968C>A (p.Pro990Thr)
c.1750C>A (p.Pro584Thr)
 gnomAD v4
15g.73323126G>ACA491478615HCN4c.2967C>T (p.Gly989=)
c.1749C>T (p.Gly583=)
 gnomAD v4
15g.73323126G>CCA491478617HCN4c.2967C>G (p.Gly989=)
c.1749C>G (p.Gly583=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73323126G=CA2187187563HCN4c.2967C= (p.Gly989=)
c.1749C= (p.Gly583=)
15g.73323126G>TCA491478620HCN4c.2967C>A (p.Gly989=)
c.1749C>A (p.Gly583=)
 gnomAD v4
15g.73323127C>ACA393086645HCN4c.2966G>T (p.Gly989Val)
c.1748G>T (p.Gly583Val)
 gnomAD v4
15g.73323127C>GCA393086646HCN4c.2966G>C (p.Gly989Ala)
c.1748G>C (p.Gly583Ala)
15g.73323127C>TCA393086648HCN4c.2966G>A (p.Gly989Asp)
c.1748G>A (p.Gly583Asp)
 gnomAD v4
15g.73323128C>ACA393086650HCN4c.2965G>T (p.Gly989Cys)
c.1747G>T (p.Gly583Cys)
 gnomAD v4
15g.73323128C>GCA393086651HCN4c.2965G>C (p.Gly989Arg)
c.1747G>C (p.Gly583Arg)
15g.73323128C>TCA393086653HCN4c.2965G>A (p.Gly989Ser)
c.1747G>A (p.Gly583Ser)
 gnomAD v4
15g.73323129A=CA2187187566HCN4c.2964T= (p.Thr988=)
c.1746T= (p.Thr582=)
15g.73323129A>CCA491478623HCN4c.2964T>G (p.Thr988=)
c.1746T>G (p.Thr582=)
15g.73323129A>GCA491478625HCN4c.2964T>C (p.Thr988=)
c.1746T>C (p.Thr582=)
 ClinVar dbSNP gnomAD v4
15g.73323129A>TCA491478629HCN4c.2964T>A (p.Thr988=)
c.1746T>A (p.Thr582=)
 gnomAD v4
15g.73323130G>ACA393086654HCN4c.2963C>T (p.Thr988Ile)
c.1745C>T (p.Thr582Ile)
 gnomAD v4
15g.73323130G>CCA393086656HCN4c.2963C>G (p.Thr988Ser)
c.1745C>G (p.Thr582Ser)
15g.73323130G>TCA393086655HCN4c.2963C>A (p.Thr988Asn)
c.1745C>A (p.Thr582Asn)
 gnomAD v4
15g.73323131T>ACA393086658HCN4c.2962A>T (p.Thr988Ser)
c.1744A>T (p.Thr582Ser)
 gnomAD v4
15g.73323131T>CCA393086660HCN4c.2962A>G (p.Thr988Ala)
c.1744A>G (p.Thr582Ala)
15g.73323131T>GCA393086661HCN4c.2962A>C (p.Thr988Pro)
c.1744A>C (p.Thr582Pro)
15g.73323132G>ACA491478635HCN4c.2961C>T (p.Ala987=)
c.1743C>T (p.Ala581=)
 gnomAD v4
15g.73323132G>CCA491478636HCN4c.2961C>G (p.Ala987=)
c.1743C>G (p.Ala581=)
15g.73323132G>TCA491478638HCN4c.2961C>A (p.Ala987=)
c.1743C>A (p.Ala581=)
 gnomAD v4
15g.73323133G>ACA393086663HCN4c.2960C>T (p.Ala987Val)
c.1742C>T (p.Ala581Val)
 gnomAD v4
15g.73323133G>CCA393086665HCN4c.2960C>G (p.Ala987Gly)
c.1742C>G (p.Ala581Gly)
15g.73323133G>TCA393086666HCN4c.2960C>A (p.Ala987Asp)
c.1742C>A (p.Ala581Asp)
 gnomAD v4
15g.73323134C>ACA393086669HCN4c.2959G>T (p.Ala987Ser)
c.1741G>T (p.Ala581Ser)
 gnomAD v4
15g.73323134C>GCA393086672HCN4c.2959G>C (p.Ala987Pro)
c.1741G>C (p.Ala581Pro)
15g.73323134C>TCA393086674HCN4c.2959G>A (p.Ala987Thr)
c.1741G>A (p.Ala581Thr)
 gnomAD v4
15g.73323135C>ACA491478644HCN4c.2958G>T (p.Leu986=)
c.1740G>T (p.Leu580=)
 gnomAD v4
15g.73323135C>GCA491478645HCN4c.2958G>C (p.Leu986=)
c.1740G>C (p.Leu580=)
15g.73323135C>TCA491478647HCN4c.2958G>A (p.Leu986=)
c.1740G>A (p.Leu580=)
 gnomAD v4
15g.73323136A>CCA393086677HCN4c.2957T>G (p.Leu986Arg)
c.1739T>G (p.Leu580Arg)
15g.73323136A>GCA393086680HCN4c.2957T>C (p.Leu986Pro)
c.1739T>C (p.Leu580Pro)
 gnomAD v4
15g.73323136A>TCA393086682HCN4c.2957T>A (p.Leu986Gln)
c.1739T>A (p.Leu580Gln)
 gnomAD v4
15g.73323137G>ACA491478651HCN4c.2956C>T (p.Leu986=)
c.1738C>T (p.Leu580=)
 gnomAD v4
15g.73323137G>CCA393086685HCN4c.2956C>G (p.Leu986Val)
c.1738C>G (p.Leu580Val)
15g.73323137G>TCA393086687HCN4c.2956C>A (p.Leu986Met)
c.1738C>A (p.Leu580Met)
 gnomAD v4

Number of alleles fetched