Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.73322810G>ACA393085795HCN4c.3283C>T (p.Gln1095Ter)
c.2065C>T (p.Gln689Ter)
 gnomAD v4
15g.73322810G>CCA393085797HCN4c.3283C>G (p.Gln1095Glu)
c.2065C>G (p.Gln689Glu)
15g.73322810G>TCA393085799HCN4c.3283C>A (p.Gln1095Lys)
c.2065C>A (p.Gln689Lys)
 gnomAD v4
15g.73322811A>CCA491477797HCN4c.3282T>G (p.Pro1094=)
c.2064T>G (p.Pro688=)
15g.73322811A>GCA491477798HCN4c.3282T>C (p.Pro1094=)
c.2064T>C (p.Pro688=)
 ClinVar gnomAD v4
15g.73322811A>TCA491477799HCN4c.3282T>A (p.Pro1094=)
c.2064T>A (p.Pro688=)
 gnomAD v4
15g.73322812G>ACA393085802HCN4c.3281C>T (p.Pro1094Leu)
c.2063C>T (p.Pro688Leu)
 gnomAD v4
15g.73322812G>CCA393085803HCN4c.3281C>G (p.Pro1094Arg)
c.2063C>G (p.Pro688Arg)
15g.73322812G>TCA393085805HCN4c.3281C>A (p.Pro1094His)
c.2063C>A (p.Pro688His)
 gnomAD v4
15g.73322813G>ACA393085809HCN4c.3280C>T (p.Pro1094Ser)
c.2062C>T (p.Pro688Ser)
 gnomAD v4
15g.73322813G>CCA393085811HCN4c.3280C>G (p.Pro1094Ala)
c.2062C>G (p.Pro688Ala)
15g.73322813G>TCA393085808HCN4c.3280C>A (p.Pro1094Thr)
c.2062C>A (p.Pro688Thr)
 gnomAD v4
15g.73322814C>ACA491477800HCN4c.3279G>T (p.Leu1093=)
c.2061G>T (p.Leu687=)
 gnomAD v4
15g.73322814C>GCA491477801HCN4c.3279G>C (p.Leu1093=)
c.2061G>C (p.Leu687=)
15g.73322814C>TCA491477802HCN4c.3279G>A (p.Leu1093=)
c.2061G>A (p.Leu687=)
 ClinVar gnomAD v4
15g.73322815A>CCA393085819HCN4c.3278T>G (p.Leu1093Arg)
c.2060T>G (p.Leu687Arg)
15g.73322815A>GCA393085814HCN4c.3278T>C (p.Leu1093Pro)
c.2060T>C (p.Leu687Pro)
15g.73322815A>TCA393085816HCN4c.3278T>A (p.Leu1093Gln)
c.2060T>A (p.Leu687Gln)
15g.73322816G>ACA491477803HCN4c.3277C>T (p.Leu1093=)
c.2059C>T (p.Leu687=)
 gnomAD v4
15g.73322816G>CCA393085820HCN4c.3277C>G (p.Leu1093Val)
c.2059C>G (p.Leu687Val)
15g.73322816G>TCA393085822HCN4c.3277C>A (p.Leu1093Met)
c.2059C>A (p.Leu687Met)
 gnomAD v4
15g.73322817G>ACA491477805HCN4c.3276C>T (p.Ala1092=)
c.2058C>T (p.Ala686=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73322817G>CCA491477806HCN4c.3276C>G (p.Ala1092=)
c.2058C>G (p.Ala686=)
15g.73322817G=CA2187186727HCN4c.3276C= (p.Ala1092=)
c.2058C= (p.Ala686=)
15g.73322817G>TCA491477804HCN4c.3276C>A (p.Ala1092=)
c.2058C>A (p.Ala686=)
 gnomAD v4
15g.73322818G>ACA393085825HCN4c.3275C>T (p.Ala1092Val)
c.2057C>T (p.Ala686Val)
 gnomAD v4
15g.73322818G>CCA393085827HCN4c.3275C>G (p.Ala1092Gly)
c.2057C>G (p.Ala686Gly)
15g.73322818G>TCA393085828HCN4c.3275C>A (p.Ala1092Asp)
c.2057C>A (p.Ala686Asp)
 ClinVar gnomAD v4
15g.73322819C>ACA393085832HCN4c.3274G>T (p.Ala1092Ser)
c.2056G>T (p.Ala686Ser)
 dbSNP gnomAD v2 gnomAD v4
15g.73322819C=CA2187186730HCN4c.3274G= (p.Ala1092=)
c.2056G= (p.Ala686=)
15g.73322819C>GCA393085834HCN4c.3274G>C (p.Ala1092Pro)
c.2056G>C (p.Ala686Pro)
15g.73322819C>TCA393085836HCN4c.3274G>A (p.Ala1092Thr)
c.2056G>A (p.Ala686Thr)
 gnomAD v4
15g.73322820T>ACA491477807HCN4c.3273A>T (p.Pro1091=)
c.2055A>T (p.Pro685=)
15g.73322820T>CCA491477808HCN4c.3273A>G (p.Pro1091=)
c.2055A>G (p.Pro685=)
15g.73322820T>GCA491477809HCN4c.3273A>C (p.Pro1091=)
c.2055A>C (p.Pro685=)
 gnomAD v4
15g.73322821G>ACA393085838HCN4c.3272C>T (p.Pro1091Leu)
c.2054C>T (p.Pro685Leu)
 gnomAD v4
15g.73322821G>CCA393085840HCN4c.3272C>G (p.Pro1091Arg)
c.2054C>G (p.Pro685Arg)
15g.73322821G>TCA393085842HCN4c.3272C>A (p.Pro1091Gln)
c.2054C>A (p.Pro685Gln)
 gnomAD v4
15g.73322822delCA2629370531HCN4c.3272del (p.Pro1091GlnfsTer?)
c.2054del (p.Pro685GlnfsTer?)
 gnomAD v4
15g.73322822G>ACA393085847HCN4c.3271C>T (p.Pro1091Ser)
c.2053C>T (p.Pro685Ser)
 gnomAD v4
15g.73322822G>CCA393085844HCN4c.3271C>G (p.Pro1091Ala)
c.2053C>G (p.Pro685Ala)
 dbSNP gnomAD v2 gnomAD v4
15g.73322822G=CA2187186734HCN4c.3271C= (p.Pro1091=)
c.2053C= (p.Pro685=)
15g.73322822G>TCA393085845HCN4c.3271C>A (p.Pro1091Thr)
c.2053C>A (p.Pro685Thr)
 gnomAD v4
15g.73322823C>ACA393085849HCN4c.3270G>T (p.Gln1090His)
c.2052G>T (p.Gln684His)
 gnomAD v4
15g.73322823C>GCA393085851HCN4c.3270G>C (p.Gln1090His)
c.2052G>C (p.Gln684His)
 gnomAD v4
15g.73322823C>TCA491477810HCN4c.3270G>A (p.Gln1090=)
c.2052G>A (p.Gln684=)
 gnomAD v4
15g.73322823_73322824delCA2575783816HCN4c.3269_3270del (p.Gln1090ProfsTer?)
c.2051_2052del (p.Gln684ProfsTer?)
15g.73322824T>ACA393085853HCN4c.3269A>T (p.Gln1090Leu)
c.2051A>T (p.Gln684Leu)
15g.73322824T>CCA393085855HCN4c.3269A>G (p.Gln1090Arg)
c.2051A>G (p.Gln684Arg)
 gnomAD v4
15g.73322824T>GCA393085857HCN4c.3269A>C (p.Gln1090Pro)
c.2051A>C (p.Gln684Pro)
15g.73322825G>ACA393085860HCN4c.3268C>T (p.Gln1090Ter)
c.2050C>T (p.Gln684Ter)
 gnomAD v4
15g.73322825G>CCA393085861HCN4c.3268C>G (p.Gln1090Glu)
c.2050C>G (p.Gln684Glu)
15g.73322825G>TCA393085864HCN4c.3268C>A (p.Gln1090Lys)
c.2050C>A (p.Gln684Lys)
 gnomAD v4
15g.73322826A>CCA491477811HCN4c.3267T>G (p.Ser1089=)
c.2049T>G (p.Ser683=)
15g.73322826A>GCA491477812HCN4c.3267T>C (p.Ser1089=)
c.2049T>C (p.Ser683=)
 ClinVar gnomAD v4
15g.73322826A>TCA491477814HCN4c.3267T>A (p.Ser1089=)
c.2049T>A (p.Ser683=)
15g.73322827G>ACA393085866HCN4c.3266C>T (p.Ser1089Phe)
c.2048C>T (p.Ser683Phe)
 gnomAD v4
15g.73322827G>CCA393085868HCN4c.3266C>G (p.Ser1089Cys)
c.2048C>G (p.Ser683Cys)
15g.73322827G>TCA393085870HCN4c.3266C>A (p.Ser1089Tyr)
c.2048C>A (p.Ser683Tyr)
 gnomAD v4
15g.73322828A>CCA393085876HCN4c.3265T>G (p.Ser1089Ala)
c.2047T>G (p.Ser683Ala)
15g.73322828A>GCA393085874HCN4c.3265T>C (p.Ser1089Pro)
c.2047T>C (p.Ser683Pro)
 gnomAD v4
15g.73322828A>TCA393085872HCN4c.3265T>A (p.Ser1089Thr)
c.2047T>A (p.Ser683Thr)
15g.73322829C>ACA491477817HCN4c.3264G>T (p.Ala1088=)
c.2046G>T (p.Ala682=)
 gnomAD v4
15g.73322829C=CA2187186737HCN4c.3264G= (p.Ala1088=)
c.2046G= (p.Ala682=)
15g.73322829C>GCA491477818HCN4c.3264G>C (p.Ala1088=)
c.2046G>C (p.Ala682=)
15g.73322829C>TCA7648855HCN4c.3264G>A (p.Ala1088=)
c.2046G>A (p.Ala682=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
15g.73322830G>ACA7648856HCN4c.3263C>T (p.Ala1088Val)
c.2045C>T (p.Ala682Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322830G>CCA393085881HCN4c.3263C>G (p.Ala1088Gly)
c.2045C>G (p.Ala682Gly)
15g.73322830G=CA2187186743HCN4c.3263C= (p.Ala1088=)
c.2045C= (p.Ala682=)
15g.73322830G>TCA393085883HCN4c.3263C>A (p.Ala1088Glu)
c.2045C>A (p.Ala682Glu)
 gnomAD v4
15g.73322831C>ACA393085885HCN4c.3262G>T (p.Ala1088Ser)
c.2044G>T (p.Ala682Ser)
 gnomAD v4
15g.73322831C=CA2187186752HCN4c.3262G= (p.Ala1088=)
c.2044G= (p.Ala682=)
15g.73322831C>GCA393085887HCN4c.3262G>C (p.Ala1088Pro)
c.2044G>C (p.Ala682Pro)
 ClinVar dbSNP gnomAD v4
15g.73322831C>TCA272663481HCN4c.3262G>A (p.Ala1088Thr)
c.2044G>A (p.Ala682Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73322832G>ACA272663495HCN4c.3261C>T (p.Ser1087=)
c.2043C>T (p.Ser681=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73322832G>CCA491477822HCN4c.3261C>G (p.Ser1087=)
c.2043C>G (p.Ser681=)
 ClinVar gnomAD v4
15g.73322832G=CA2187186756HCN4c.3261C= (p.Ser1087=)
c.2043C= (p.Ser681=)
15g.73322832G>TCA491477823HCN4c.3261C>A (p.Ser1087=)
c.2043C>A (p.Ser681=)
 dbSNP gnomAD v2 gnomAD v4
15g.73322833G>ACA393085892HCN4c.3260C>T (p.Ser1087Phe)
c.2042C>T (p.Ser681Phe)
 ClinVar gnomAD v4
15g.73322833G>CCA393085894HCN4c.3260C>G (p.Ser1087Cys)
c.2042C>G (p.Ser681Cys)
15g.73322833G>TCA393085896HCN4c.3260C>A (p.Ser1087Tyr)
c.2042C>A (p.Ser681Tyr)
 gnomAD v4
15g.73322834A=CA2187186760HCN4c.3259T= (p.Ser1087=)
c.2041T= (p.Ser681=)
15g.73322834A>CCA393085897HCN4c.3259T>G (p.Ser1087Ala)
c.2041T>G (p.Ser681Ala)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73322834A>GCA393085899HCN4c.3259T>C (p.Ser1087Pro)
c.2041T>C (p.Ser681Pro)
 gnomAD v4
15g.73322834A>TCA393085901HCN4c.3259T>A (p.Ser1087Thr)
c.2041T>A (p.Ser681Thr)
15g.73322835G>ACA491477826HCN4c.3258C>T (p.Ile1086=)
c.2040C>T (p.Ile680=)
15g.73322835G>CCA393085903HCN4c.3258C>G (p.Ile1086Met)
c.2040C>G (p.Ile680Met)
15g.73322835G>TCA491477827HCN4c.3258C>A (p.Ile1086=)
c.2040C>A (p.Ile680=)
 gnomAD v4
15g.73322837_73322839dupCA2580089970HCN4c.3256_3258dup (p.Ile1086_Ser1087insIle)
c.2038_2040dup (p.Ile680_Ser681insIle)
 ClinVar
15g.73322836_73322847delCA2697549179HCN4c.3247_3258del (p.Leu1083_Ile1086del)
c.2029_2040del (p.Leu677_Ile680del)
 ClinVar
15g.73322836A>CCA393085905HCN4c.3257T>G (p.Ile1086Ser)
c.2039T>G (p.Ile680Ser)
15g.73322836A>GCA393085907HCN4c.3257T>C (p.Ile1086Thr)
c.2039T>C (p.Ile680Thr)
 gnomAD v4
15g.73322836A>TCA393085909HCN4c.3257T>A (p.Ile1086Asn)
c.2039T>A (p.Ile680Asn)
 gnomAD v4
15g.73322837T>ACA393085912HCN4c.3256A>T (p.Ile1086Phe)
c.2038A>T (p.Ile680Phe)
15g.73322837T>CCA393085913HCN4c.3256A>G (p.Ile1086Val)
c.2038A>G (p.Ile680Val)
 gnomAD v4
15g.73322837T>GCA393085916HCN4c.3256A>C (p.Ile1086Leu)
c.2038A>C (p.Ile680Leu)
 dbSNP gnomAD v4
15g.73322838G>ACA491477828HCN4c.3255C>T (p.Leu1085=)
c.2037C>T (p.Leu679=)
 gnomAD v4
15g.73322838G>CCA491477831HCN4c.3255C>G (p.Leu1085=)
c.2037C>G (p.Leu679=)
15g.73322838G=CA2187186765HCN4c.3255C= (p.Leu1085=)
c.2037C= (p.Leu679=)
15g.73322838G>TCA491477829HCN4c.3255C>A (p.Leu1085=)
c.2037C>A (p.Leu679=)
 dbSNP gnomAD v2 gnomAD v4
15g.73322839A=CA2187186769HCN4c.3254T= (p.Leu1085=)
c.2036T= (p.Leu679=)
15g.73322839A>CCA393085918HCN4c.3254T>G (p.Leu1085Arg)
c.2036T>G (p.Leu679Arg)
15g.73322839A>GCA393085920HCN4c.3254T>C (p.Leu1085Pro)
c.2036T>C (p.Leu679Pro)
 gnomAD v4
15g.73322839A>TCA393085922HCN4c.3254T>A (p.Leu1085His)
c.2036T>A (p.Leu679His)
 dbSNP gnomAD v4
15g.73322840G>ACA7648857HCN4c.3253C>T (p.Leu1085Phe)
c.2035C>T (p.Leu679Phe)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.73322840G>CCA393085924HCN4c.3253C>G (p.Leu1085Val)
c.2035C>G (p.Leu679Val)
 dbSNP gnomAD v2 gnomAD v4
15g.73322840G=CA2187186772HCN4c.3253C= (p.Leu1085=)
c.2035C= (p.Leu679=)
15g.73322840G>TCA393085925HCN4c.3253C>A (p.Leu1085Ile)
c.2035C>A (p.Leu679Ile)
 gnomAD v4
15g.73322841C>ACA393085926HCN4c.3252G>T (p.Lys1084Asn)
c.2034G>T (p.Lys678Asn)
 gnomAD v4
15g.73322841C=CA2187186774HCN4c.3252G= (p.Lys1084=)
c.2034G= (p.Lys678=)
15g.73322841C>GCA393085927HCN4c.3252G>C (p.Lys1084Asn)
c.2034G>C (p.Lys678Asn)
 gnomAD v4
15g.73322841C>TCA272663516HCN4c.3252G>A (p.Lys1084=)
c.2034G>A (p.Lys678=)
 dbSNP gnomAD v4
15g.73322842T>ACA7648858HCN4c.3251A>T (p.Lys1084Met)
c.2033A>T (p.Lys678Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.73322842T>CCA393085929HCN4c.3251A>G (p.Lys1084Arg)
c.2033A>G (p.Lys678Arg)
 dbSNP gnomAD v3 gnomAD v4
15g.73322842T>GCA393085928HCN4c.3251A>C (p.Lys1084Thr)
c.2033A>C (p.Lys678Thr)
15g.73322842T=CA2187186777HCN4c.3251A= (p.Lys1084=)
c.2033A= (p.Lys678=)
15g.73322843T>ACA393085932HCN4c.3250A>T (p.Lys1084Ter)
c.2032A>T (p.Lys678Ter)
15g.73322843T>CCA393085930HCN4c.3250A>G (p.Lys1084Glu)
c.2032A>G (p.Lys678Glu)
 dbSNP gnomAD v4
15g.73322843T>GCA393085931HCN4c.3250A>C (p.Lys1084Gln)
c.2032A>C (p.Lys678Gln)
15g.73322843T=CA2187186778HCN4c.3250A= (p.Lys1084=)
c.2032A= (p.Lys678=)
15g.73322844G>ACA7648859HCN4c.3249C>T (p.Leu1083=)
c.2031C>T (p.Leu677=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.73322844G>CCA491477835HCN4c.3249C>G (p.Leu1083=)
c.2031C>G (p.Leu677=)
15g.73322844G=CA2187186780HCN4c.3249C= (p.Leu1083=)
c.2031C= (p.Leu677=)
15g.73322844G>TCA491477836HCN4c.3249C>A (p.Leu1083=)
c.2031C>A (p.Leu677=)
 gnomAD v4
15g.73322845A>CCA393085933HCN4c.3248T>G (p.Leu1083Arg)
c.2030T>G (p.Leu677Arg)
 gnomAD v4
15g.73322845A>GCA393085934HCN4c.3248T>C (p.Leu1083Pro)
c.2030T>C (p.Leu677Pro)
 gnomAD v4
15g.73322845A>TCA393085935HCN4c.3248T>A (p.Leu1083His)
c.2030T>A (p.Leu677His)
 gnomAD v4
15g.73322846G>ACA393085936HCN4c.3247C>T (p.Leu1083Phe)
c.2029C>T (p.Leu677Phe)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73322846G>CCA393085937HCN4c.3247C>G (p.Leu1083Val)
c.2029C>G (p.Leu677Val)
 gnomAD v4
15g.73322846G=CA2187186782HCN4c.3247C= (p.Leu1083=)
c.2029C= (p.Leu677=)
15g.73322846G>TCA393085938HCN4c.3247C>A (p.Leu1083Ile)
c.2029C>A (p.Leu677Ile)
 gnomAD v4
15g.73322847G>ACA491477838HCN4c.3246C>T (p.Asp1082=)
c.2028C>T (p.Asp676=)
 dbSNP gnomAD v4
15g.73322847G>CCA393085939HCN4c.3246C>G (p.Asp1082Glu)
c.2028C>G (p.Asp676Glu)
15g.73322847G=CA2187186784HCN4c.3246C= (p.Asp1082=)
c.2028C= (p.Asp676=)
15g.73322847G>TCA393085940HCN4c.3246C>A (p.Asp1082Glu)
c.2028C>A (p.Asp676Glu)
 gnomAD v4
15g.73322848T>ACA393085941HCN4c.3245A>T (p.Asp1082Val)
c.2027A>T (p.Asp676Val)
15g.73322848T>CCA393085942HCN4c.3245A>G (p.Asp1082Gly)
c.2027A>G (p.Asp676Gly)
15g.73322848T>GCA393085943HCN4c.3245A>C (p.Asp1082Ala)
c.2027A>C (p.Asp676Ala)
15g.73322849C>ACA393085946HCN4c.3244G>T (p.Asp1082Tyr)
c.2026G>T (p.Asp676Tyr)
 dbSNP gnomAD v2 gnomAD v4
15g.73322849C=CA2187186786HCN4c.3244G= (p.Asp1082=)
c.2026G= (p.Asp676=)
15g.73322849C>GCA393085945HCN4c.3244G>C (p.Asp1082His)
c.2026G>C (p.Asp676His)
15g.73322849C>TCA393085944HCN4c.3244G>A (p.Asp1082Asn)
c.2026G>A (p.Asp676Asn)
 gnomAD v4
15g.73322850C>ACA393085947HCN4c.3243G>T (p.Gln1081His)
c.2025G>T (p.Gln675His)
 gnomAD v4
15g.73322850C=CA2187186789HCN4c.3243G= (p.Gln1081=)
c.2025G= (p.Gln675=)
15g.73322850C>GCA393085948HCN4c.3243G>C (p.Gln1081His)
c.2025G>C (p.Gln675His)
15g.73322850C>TCA491477843HCN4c.3243G>A (p.Gln1081=)
c.2025G>A (p.Gln675=)
 ClinVar dbSNP gnomAD v4
15g.73322851T>ACA393085949HCN4c.3242A>T (p.Gln1081Leu)
c.2024A>T (p.Gln675Leu)
15g.73322851T>CCA393085950HCN4c.3242A>G (p.Gln1081Arg)
c.2024A>G (p.Gln675Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73322851T>GCA393085951HCN4c.3242A>C (p.Gln1081Pro)
c.2024A>C (p.Gln675Pro)
15g.73322851T=CA2187186791HCN4c.3242A= (p.Gln1081=)
c.2024A= (p.Gln675=)
15g.73322852G>ACA393085952HCN4c.3241C>T (p.Gln1081Ter)
c.2023C>T (p.Gln675Ter)
 gnomAD v4
15g.73322852G>CCA393085953HCN4c.3241C>G (p.Gln1081Glu)
c.2023C>G (p.Gln675Glu)
15g.73322852G>TCA393085954HCN4c.3241C>A (p.Gln1081Lys)
c.2023C>A (p.Gln675Lys)
 gnomAD v4
15g.73322853G>ACA491477846HCN4c.3240C>T (p.Thr1080=)
c.2022C>T (p.Thr674=)
 gnomAD v4
15g.73322853G>CCA491477847HCN4c.3240C>G (p.Thr1080=)
c.2022C>G (p.Thr674=)
15g.73322853G>TCA491477848HCN4c.3240C>A (p.Thr1080=)
c.2022C>A (p.Thr674=)
 gnomAD v4
15g.73322854G>ACA393085955HCN4c.3239C>T (p.Thr1080Ile)
c.2021C>T (p.Thr674Ile)
 gnomAD v4
15g.73322854G>CCA393085956HCN4c.3239C>G (p.Thr1080Ser)
c.2021C>G (p.Thr674Ser)
15g.73322854G>TCA393085957HCN4c.3239C>A (p.Thr1080Asn)
c.2021C>A (p.Thr674Asn)
 gnomAD v4
15g.73322855T>ACA393085958HCN4c.3238A>T (p.Thr1080Ser)
c.2020A>T (p.Thr674Ser)
15g.73322855T>CCA393085959HCN4c.3238A>G (p.Thr1080Ala)
c.2020A>G (p.Thr674Ala)
 gnomAD v4
15g.73322855T>GCA393085960HCN4c.3238A>C (p.Thr1080Pro)
c.2020A>C (p.Thr674Pro)
15g.73322856G>ACA491477852HCN4c.3237C>T (p.Leu1079=)
c.2019C>T (p.Leu673=)
 gnomAD v4
15g.73322856G>CCA491477853HCN4c.3237C>G (p.Leu1079=)
c.2019C>G (p.Leu673=)
15g.73322856G>TCA491477854HCN4c.3237C>A (p.Leu1079=)
c.2019C>A (p.Leu673=)
 gnomAD v4
15g.73322857A>CCA393085962HCN4c.3236T>G (p.Leu1079Arg)
c.2018T>G (p.Leu673Arg)
15g.73322857A>GCA393085963HCN4c.3236T>C (p.Leu1079Pro)
c.2018T>C (p.Leu673Pro)
 gnomAD v4
15g.73322857A>TCA393085961HCN4c.3236T>A (p.Leu1079His)
c.2018T>A (p.Leu673His)
 gnomAD v4
15g.73322858G>ACA393085964HCN4c.3235C>T (p.Leu1079Phe)
c.2017C>T (p.Leu673Phe)
 gnomAD v4
15g.73322858G>CCA393085965HCN4c.3235C>G (p.Leu1079Val)
c.2017C>G (p.Leu673Val)
15g.73322858G>TCA393085966HCN4c.3235C>A (p.Leu1079Ile)
c.2017C>A (p.Leu673Ile)
 gnomAD v4
15g.73322859G>ACA272663525HCN4c.3234C>T (p.Arg1078=)
c.2016C>T (p.Arg672=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
15g.73322859G>CCA491477856HCN4c.3234C>G (p.Arg1078=)
c.2016C>G (p.Arg672=)
15g.73322859G=CA2187186794HCN4c.3234C= (p.Arg1078=)
c.2016C= (p.Arg672=)
15g.73322859G>TCA491477857HCN4c.3234C>A (p.Arg1078=)
c.2016C>A (p.Arg672=)
 gnomAD v4
15g.73322860C>ACA393085967HCN4c.3233G>T (p.Arg1078Leu)
c.2015G>T (p.Arg672Leu)
 gnomAD v4
15g.73322860C=CA2187186796HCN4c.3233G= (p.Arg1078=)
c.2015G= (p.Arg672=)
15g.73322860C>GCA393085968HCN4c.3233G>C (p.Arg1078Pro)
c.2015G>C (p.Arg672Pro)
15g.73322860C>TCA393085969HCN4c.3233G>A (p.Arg1078His)
c.2015G>A (p.Arg672His)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
15g.73322861G>ACA7648860HCN4c.3232C>T (p.Arg1078Cys)
c.2014C>T (p.Arg672Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322861G>CCA393085970HCN4c.3232C>G (p.Arg1078Gly)
c.2014C>G (p.Arg672Gly)
 gnomAD v4
15g.73322861G=CA2187186801HCN4c.3232C= (p.Arg1078=)
c.2014C= (p.Arg672=)
15g.73322861G>TCA393085971HCN4c.3232C>A (p.Arg1078Ser)
c.2014C>A (p.Arg672Ser)
 gnomAD v4
15g.73322862G>ACA491477859HCN4c.3231C>T (p.Gly1077=)
c.2013C>T (p.Gly671=)
 gnomAD v4
15g.73322862G>CCA491477860HCN4c.3231C>G (p.Gly1077=)
c.2013C>G (p.Gly671=)
15g.73322862G=CA2187186805HCN4c.3231C= (p.Gly1077=)
c.2013C= (p.Gly671=)
15g.73322862G>TCA491477861HCN4c.3231C>A (p.Gly1077=)
c.2013C>A (p.Gly671=)
 dbSNP gnomAD v4
15g.73322863C>ACA393085972HCN4c.3230G>T (p.Gly1077Val)
c.2012G>T (p.Gly671Val)
 gnomAD v4
15g.73322863C>GCA393085973HCN4c.3230G>C (p.Gly1077Ala)
c.2012G>C (p.Gly671Ala)
15g.73322863C>TCA393085974HCN4c.3230G>A (p.Gly1077Asp)
c.2012G>A (p.Gly671Asp)
 gnomAD v4
15g.73322864C>ACA393085975HCN4c.3229G>T (p.Gly1077Cys)
c.2011G>T (p.Gly671Cys)
 gnomAD v4
15g.73322864C=CA2187186813HCN4c.3229G= (p.Gly1077=)
c.2011G= (p.Gly671=)
15g.73322864C>GCA393085976HCN4c.3229G>C (p.Gly1077Arg)
c.2011G>C (p.Gly671Arg)
 gnomAD v4
15g.73322864C>TCA7648861HCN4c.3229G>A (p.Gly1077Ser)
c.2011G>A (p.Gly671Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322872_73322881dupCA2629370532HCN4c.3220_3229dup (p.Gly1077AlafsTer?)
c.2002_2011dup (p.Gly671AlafsTer?)
 gnomAD v4
15g.73322872_73322881delCA2629370533HCN4c.3220_3229del (p.Leu1074AlafsTer?)
c.2002_2011del (p.Leu668AlafsTer?)
 gnomAD v4
15g.73322865G>ACA7648862HCN4c.3228C>T (p.Pro1076=)
c.2010C>T (p.Pro670=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322865G>CCA491477864HCN4c.3228C>G (p.Pro1076=)
c.2010C>G (p.Pro670=)
 dbSNP gnomAD v2 gnomAD v4 COSMIC
15g.73322865G=CA2187186821HCN4c.3228C= (p.Pro1076=)
c.2010C= (p.Pro670=)
15g.73322865G>TCA491477865HCN4c.3228C>A (p.Pro1076=)
c.2010C>A (p.Pro670=)
 gnomAD v4
15g.73322869delCA619410582HCN4c.3228del (p.Gly1077AlafsTer?)
c.2010del (p.Gly671AlafsTer?)
 gnomAD v2 gnomAD v4
15g.73322866G>ACA393085977HCN4c.3227C>T (p.Pro1076Leu)
c.2009C>T (p.Pro670Leu)
 dbSNP
15g.73322866G>CCA393085978HCN4c.3227C>G (p.Pro1076Arg)
c.2009C>G (p.Pro670Arg)
15g.73322866G=CA2187186825HCN4c.3227C= (p.Pro1076=)
c.2009C= (p.Pro670=)
15g.73322866G>TCA393085979HCN4c.3227C>A (p.Pro1076His)
c.2009C>A (p.Pro670His)
 dbSNP gnomAD v2 gnomAD v4
15g.73322867G>ACA393085982HCN4c.3226C>T (p.Pro1076Ser)
c.2008C>T (p.Pro670Ser)
 gnomAD v4
15g.73322867G>CCA393085981HCN4c.3226C>G (p.Pro1076Ala)
c.2008C>G (p.Pro670Ala)
15g.73322867G=CA2187186828HCN4c.3226C= (p.Pro1076=)
c.2008C= (p.Pro670=)
15g.73322867G>TCA393085980HCN4c.3226C>A (p.Pro1076Thr)
c.2008C>A (p.Pro670Thr)
 dbSNP gnomAD v2 gnomAD v4
15g.73322868G>ACA491477869HCN4c.3225C>T (p.Thr1075=)
c.2007C>T (p.Thr669=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73322868G>CCA491477870HCN4c.3225C>G (p.Thr1075=)
c.2007C>G (p.Thr669=)
15g.73322868G=CA2187186831HCN4c.3225C= (p.Thr1075=)
c.2007C= (p.Thr669=)
15g.73322868G>TCA491477871HCN4c.3225C>A (p.Thr1075=)
c.2007C>A (p.Thr669=)
 gnomAD v4
15g.73322869_73322871delCA2740096730HCN4c.3223_3225del (p.Thr1075del)
c.2005_2007del (p.Thr669del)
 ClinVar
15g.73322869G>ACA272663542HCN4c.3224C>T (p.Thr1075Ile)
c.2006C>T (p.Thr669Ile)
 dbSNP gnomAD v4
15g.73322869G>CCA393085983HCN4c.3224C>G (p.Thr1075Ser)
c.2006C>G (p.Thr669Ser)
 gnomAD v4
15g.73322869G=CA2187186835HCN4c.3224C= (p.Thr1075=)
c.2006C= (p.Thr669=)
15g.73322869G>TCA393085984HCN4c.3224C>A (p.Thr1075Asn)
c.2006C>A (p.Thr669Asn)
 gnomAD v4
15g.73322870T>ACA393085985HCN4c.3223A>T (p.Thr1075Ser)
c.2005A>T (p.Thr669Ser)
15g.73322870T>CCA7648863HCN4c.3223A>G (p.Thr1075Ala)
c.2005A>G (p.Thr669Ala)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.73322870T>GCA272663548HCN4c.3223A>C (p.Thr1075Pro)
c.2005A>C (p.Thr669Pro)
 dbSNP
15g.73322870T=CA2187186843HCN4c.3223A= (p.Thr1075=)
c.2005A= (p.Thr669=)
15g.73322870_73322897delinsTGAGCGGGGGTGTGCCCCGGCGCTGGGGCA2187186841HCN4c.3196_3223delinsCCCCAGCGCCGGGGCACACCCCCGCTCA (p.Pro1066=)
c.1978_2005delinsCCCCAGCGCCGGGGCACACCCCCGCTCA (p.Pro660=)
15g.73322871G>ACA491477877HCN4c.3222C>T (p.Leu1074=)
c.2004C>T (p.Leu668=)
 gnomAD v4
15g.73322871G>CCA491477876HCN4c.3222C>G (p.Leu1074=)
c.2004C>G (p.Leu668=)
 gnomAD v4
15g.73322871G>TCA491477875HCN4c.3222C>A (p.Leu1074=)
c.2004C>A (p.Leu668=)
 gnomAD v4
15g.73322873_73322899delCA2187186847HCN4c.3196_3222del (p.Pro1066_Leu1074del)
c.1978_2004del (p.Pro660_Leu668del)
 dbSNP
15g.73322872A>CCA393085986HCN4c.3221T>G (p.Leu1074Arg)
c.2003T>G (p.Leu668Arg)
15g.73322872A>GCA393085988HCN4c.3221T>C (p.Leu1074Pro)
c.2003T>C (p.Leu668Pro)
 gnomAD v4
15g.73322872A>TCA393085987HCN4c.3221T>A (p.Leu1074His)
c.2003T>A (p.Leu668His)
15g.73322873G>ACA7648864HCN4c.3220C>T (p.Leu1074Phe)
c.2002C>T (p.Leu668Phe)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322873G>CCA393085990HCN4c.3220C>G (p.Leu1074Val)
c.2002C>G (p.Leu668Val)
15g.73322873G=CA2187186850HCN4c.3220C= (p.Leu1074=)
c.2002C= (p.Leu668=)
15g.73322873G>TCA393085989HCN4c.3220C>A (p.Leu1074Ile)
c.2002C>A (p.Leu668Ile)
 gnomAD v4
15g.73322874C>ACA491477893HCN4c.3219G>T (p.Pro1073=)
c.2001G>T (p.Pro667=)
 gnomAD v4
15g.73322874C=CA2187186855HCN4c.3219G= (p.Pro1073=)
c.2001G= (p.Pro667=)
15g.73322874C>GCA491477895HCN4c.3219G>C (p.Pro1073=)
c.2001G>C (p.Pro667=)
15g.73322874C>TCA491477896HCN4c.3219G>A (p.Pro1073=)
c.2001G>A (p.Pro667=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
15g.73322875G>ACA7648865HCN4c.3218C>T (p.Pro1073Leu)
c.2000C>T (p.Pro667Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322875G>CCA272663565HCN4c.3218C>G (p.Pro1073Arg)
c.2000C>G (p.Pro667Arg)
 ClinVar dbSNP gnomAD v4
15g.73322875G=CA2187186860HCN4c.3218C= (p.Pro1073=)
c.2000C= (p.Pro667=)
15g.73322875G>TCA393085991HCN4c.3218C>A (p.Pro1073Gln)
c.2000C>A (p.Pro667Gln)
 gnomAD v4
15g.73322879delCA2575783817HCN4c.3218del (p.Pro1073ArgfsTer?)
c.2000del (p.Pro667ArgfsTer?)
 gnomAD v4
15g.73322875_73322902delinsGGGGGTGTGCCCCGGCGCTGGGGGACCTCA2187186862HCN4c.3191_3218delinsAGGTCCCCCAGCGCCGGGGCACACCCCC (p.Gln1064=)
c.1973_2000delinsAGGTCCCCCAGCGCCGGGGCACACCCCC (p.Gln658=)
15g.73322876G>ACA393085992HCN4c.3217C>T (p.Pro1073Ser)
c.1999C>T (p.Pro667Ser)
 gnomAD v4
15g.73322876G>CCA393085993HCN4c.3217C>G (p.Pro1073Ala)
c.1999C>G (p.Pro667Ala)
15g.73322876G>TCA393085994HCN4c.3217C>A (p.Pro1073Thr)
c.1999C>A (p.Pro667Thr)
 gnomAD v4
15g.73322882_73322908delCA7648866HCN4c.3191_3217del (p.Gln1064_Pro1072del)
c.1973_1999del (p.Gln658_Pro666del)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322877G>ACA491477897HCN4c.3216C>T (p.Pro1072=)
c.1998C>T (p.Pro666=)
 gnomAD v4
15g.73322877G>CCA491477898HCN4c.3216C>G (p.Pro1072=)
c.1998C>G (p.Pro666=)
15g.73322877G>TCA491477899HCN4c.3216C>A (p.Pro1072=)
c.1998C>A (p.Pro666=)
 gnomAD v4
15g.73322878G>ACA393085995HCN4c.3215C>T (p.Pro1072Leu)
c.1997C>T (p.Pro666Leu)
15g.73322878G>CCA393085996HCN4c.3215C>G (p.Pro1072Arg)
c.1997C>G (p.Pro666Arg)
15g.73322878G>TCA393085997HCN4c.3215C>A (p.Pro1072His)
c.1997C>A (p.Pro666His)
 gnomAD v4
15g.73322879G>ACA7648867HCN4c.3214C>T (p.Pro1072Ser)
c.1996C>T (p.Pro666Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322879G>CCA393085998HCN4c.3214C>G (p.Pro1072Ala)
c.1996C>G (p.Pro666Ala)
15g.73322879G=CA2187186870HCN4c.3214C= (p.Pro1072=)
c.1996C= (p.Pro666=)
15g.73322879G>TCA393085999HCN4c.3214C>A (p.Pro1072Thr)
c.1996C>A (p.Pro666Thr)
 gnomAD v4
15g.73322880T>ACA491477902HCN4c.3213A>T (p.Thr1071=)
c.1995A>T (p.Thr665=)
 gnomAD v4
15g.73322880T>CCA491477903HCN4c.3213A>G (p.Thr1071=)
c.1995A>G (p.Thr665=)
 dbSNP
15g.73322880T>GCA491477904HCN4c.3213A>C (p.Thr1071=)
c.1995A>C (p.Thr665=)
 dbSNP gnomAD v3 gnomAD v4
15g.73322880T=CA2187186874HCN4c.3213A= (p.Thr1071=)
c.1995A= (p.Thr665=)
15g.73322881G>ACA393086000HCN4c.3212C>T (p.Thr1071Ile)
c.1994C>T (p.Thr665Ile)
 ClinVar gnomAD v4
15g.73322881G>CCA393086002HCN4c.3212C>G (p.Thr1071Arg)
c.1994C>G (p.Thr665Arg)
15g.73322881G>TCA393086001HCN4c.3212C>A (p.Thr1071Lys)
c.1994C>A (p.Thr665Lys)
 gnomAD v4
15g.73322882T>ACA393086003HCN4c.3211A>T (p.Thr1071Ser)
c.1993A>T (p.Thr665Ser)
 gnomAD v4
15g.73322882T>CCA393086004HCN4c.3211A>G (p.Thr1071Ala)
c.1993A>G (p.Thr665Ala)
 gnomAD v4
15g.73322882T>GCA393086005HCN4c.3211A>C (p.Thr1071Pro)
c.1993A>C (p.Thr665Pro)
 gnomAD v4
15g.73322883G>ACA491477908HCN4c.3210C>T (p.Gly1070=)
c.1992C>T (p.Gly664=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73322883G>CCA491477909HCN4c.3210C>G (p.Gly1070=)
c.1992C>G (p.Gly664=)
 gnomAD v4
15g.73322883G=CA2187186883HCN4c.3210C= (p.Gly1070=)
c.1992C= (p.Gly664=)
15g.73322883G>TCA491477910HCN4c.3210C>A (p.Gly1070=)
c.1992C>A (p.Gly664=)
 gnomAD v4
15g.73322884C>ACA393086006HCN4c.3209G>T (p.Gly1070Val)
c.1991G>T (p.Gly664Val)
 gnomAD v4
15g.73322884C=CA2187186887HCN4c.3209G= (p.Gly1070=)
c.1991G= (p.Gly664=)
15g.73322884C>GCA393086007HCN4c.3209G>C (p.Gly1070Ala)
c.1991G>C (p.Gly664Ala)
15g.73322884C>TCA7648868HCN4c.3209G>A (p.Gly1070Asp)
c.1991G>A (p.Gly664Asp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322887delCA2575783818HCN4c.3209del (p.Gly1070AlafsTer?)
c.1991del (p.Gly664AlafsTer?)
 gnomAD v4
15g.73322885C>ACA393086008HCN4c.3208G>T (p.Gly1070Cys)
c.1990G>T (p.Gly664Cys)
15g.73322885C>GCA393086009HCN4c.3208G>C (p.Gly1070Arg)
c.1990G>C (p.Gly664Arg)
15g.73322885C>TCA393086010HCN4c.3208G>A (p.Gly1070Ser)
c.1990G>A (p.Gly664Ser)
15g.73322886C>ACA491477918HCN4c.3207G>T (p.Arg1069=)
c.1989G>T (p.Arg663=)
 gnomAD v4
15g.73322886C>GCA491477915HCN4c.3207G>C (p.Arg1069=)
c.1989G>C (p.Arg663=)
15g.73322886C>TCA491477914HCN4c.3207G>A (p.Arg1069=)
c.1989G>A (p.Arg663=)
 gnomAD v4
15g.73322887C>ACA393086012HCN4c.3206G>T (p.Arg1069Leu)
c.1988G>T (p.Arg663Leu)
 ClinVar dbSNP gnomAD v3 gnomAD v4
15g.73322887C=CA2187186890HCN4c.3206G= (p.Arg1069=)
c.1988G= (p.Arg663=)
15g.73322887C>GCA393086011HCN4c.3206G>C (p.Arg1069Pro)
c.1988G>C (p.Arg663Pro)
 dbSNP gnomAD v4
15g.73322887C>TCA7648869HCN4c.3206G>A (p.Arg1069Gln)
c.1988G>A (p.Arg663Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322888G>ACA7648870HCN4c.3205C>T (p.Arg1069Trp)
c.1987C>T (p.Arg663Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322888G>CCA393086013HCN4c.3205C>G (p.Arg1069Gly)
c.1987C>G (p.Arg663Gly)
 dbSNP gnomAD v3 gnomAD v4
15g.73322888G=CA2187186901HCN4c.3205C= (p.Arg1069=)
c.1987C= (p.Arg663=)
15g.73322888G>TCA491477920HCN4c.3205C>A (p.Arg1069=)
c.1987C>A (p.Arg663=)
 gnomAD v4
15g.73322889G>ACA491477922HCN4c.3204C>T (p.Arg1068=)
c.1986C>T (p.Arg662=)
 gnomAD v4
15g.73322889G>CCA491477924HCN4c.3204C>G (p.Arg1068=)
c.1986C>G (p.Arg662=)
15g.73322889G>TCA491477925HCN4c.3204C>A (p.Arg1068=)
c.1986C>A (p.Arg662=)
 gnomAD v4
15g.73322890C>ACA393086014HCN4c.3203G>T (p.Arg1068Leu)
c.1985G>T (p.Arg662Leu)
 gnomAD v4
15g.73322890C=CA2187186903HCN4c.3203G= (p.Arg1068=)
c.1985G= (p.Arg662=)
15g.73322890C>GCA393086015HCN4c.3203G>C (p.Arg1068Pro)
c.1985G>C (p.Arg662Pro)
 ClinVar dbSNP gnomAD v2
15g.73322890C>TCA7648871HCN4c.3203G>A (p.Arg1068His)
c.1985G>A (p.Arg662His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322891G>ACA7648872HCN4c.3202C>T (p.Arg1068Cys)
c.1984C>T (p.Arg662Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
15g.73322891G>CCA393086016HCN4c.3202C>G (p.Arg1068Gly)
c.1984C>G (p.Arg662Gly)
15g.73322891G=CA2187186909HCN4c.3202C= (p.Arg1068=)
c.1984C= (p.Arg662=)
15g.73322891G>TCA393086017HCN4c.3202C>A (p.Arg1068Ser)
c.1984C>A (p.Arg662Ser)
 ClinVar gnomAD v4
15g.73322892C>ACA393086018HCN4c.3201G>T (p.Gln1067His)
c.1983G>T (p.Gln661His)
 gnomAD v4
15g.73322892C>GCA393086019HCN4c.3201G>C (p.Gln1067His)
c.1983G>C (p.Gln661His)
15g.73322892C>TCA491477929HCN4c.3201G>A (p.Gln1067=)
c.1983G>A (p.Gln661=)
 gnomAD v4
15g.73322893T>ACA393086020HCN4c.3200A>T (p.Gln1067Leu)
c.1982A>T (p.Gln661Leu)
15g.73322893T>CCA393086021HCN4c.3200A>G (p.Gln1067Arg)
c.1982A>G (p.Gln661Arg)
 gnomAD v4
15g.73322893T>GCA393086022HCN4c.3200A>C (p.Gln1067Pro)
c.1982A>C (p.Gln661Pro)
 dbSNP gnomAD v3 gnomAD v4
15g.73322893T=CA2187186915HCN4c.3200A= (p.Gln1067=)
c.1982A= (p.Gln661=)
15g.73322894G>ACA393086025HCN4c.3199C>T (p.Gln1067Ter)
c.1981C>T (p.Gln661Ter)
 gnomAD v4
15g.73322894G>CCA393086023HCN4c.3199C>G (p.Gln1067Glu)
c.1981C>G (p.Gln661Glu)
15g.73322894G>TCA393086024HCN4c.3199C>A (p.Gln1067Lys)
c.1981C>A (p.Gln661Lys)
 gnomAD v4
15g.73322898delCA2575783819HCN4c.3199del (p.Gln1067SerfsTer?)
c.1981del (p.Gln661SerfsTer?)
 gnomAD v4
15g.73322895G>ACA491477931HCN4c.3198C>T (p.Pro1066=)
c.1980C>T (p.Pro660=)
 gnomAD v4
15g.73322895G>CCA491477932HCN4c.3198C>G (p.Pro1066=)
c.1980C>G (p.Pro660=)
15g.73322895G>TCA491477933HCN4c.3198C>A (p.Pro1066=)
c.1980C>A (p.Pro660=)
 gnomAD v4
15g.73322896G>ACA393086026HCN4c.3197C>T (p.Pro1066Leu)
c.1979C>T (p.Pro660Leu)
 gnomAD v4
15g.73322896G>CCA393086027HCN4c.3197C>G (p.Pro1066Arg)
c.1979C>G (p.Pro660Arg)
15g.73322896G=CA2187186921HCN4c.3197C= (p.Pro1066=)
c.1979C= (p.Pro660=)
15g.73322896G>TCA247667HCN4c.3197C>A (p.Pro1066His)
c.1979C>A (p.Pro660His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322897G>ACA393086028HCN4c.3196C>T (p.Pro1066Ser)
c.1978C>T (p.Pro660Ser)
 gnomAD v4
15g.73322897G>CCA393086029HCN4c.3196C>G (p.Pro1066Ala)
c.1978C>G (p.Pro660Ala)
15g.73322897G>TCA393086030HCN4c.3196C>A (p.Pro1066Thr)
c.1978C>A (p.Pro660Thr)
 gnomAD v4
15g.73322898G>ACA491477938HCN4c.3195C>T (p.Val1065=)
c.1977C>T (p.Val659=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73322898G>CCA272663629HCN4c.3195C>G (p.Val1065=)
c.1977C>G (p.Val659=)
 dbSNP gnomAD v4
15g.73322898G=CA2187186925HCN4c.3195C= (p.Val1065=)
c.1977C= (p.Val659=)
15g.73322898G>TCA7648873HCN4c.3195C>A (p.Val1065=)
c.1977C>A (p.Val659=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322899A=CA2187186933HCN4c.3194T= (p.Val1065=)
c.1976T= (p.Val659=)
15g.73322899A>CCA393086031HCN4c.3194T>G (p.Val1065Gly)
c.1976T>G (p.Val659Gly)
 gnomAD v4
15g.73322899A>GCA393086032HCN4c.3194T>C (p.Val1065Ala)
c.1976T>C (p.Val659Ala)
 ClinVar dbSNP gnomAD v4
15g.73322899A>TCA393086033HCN4c.3194T>A (p.Val1065Asp)
c.1976T>A (p.Val659Asp)
15g.73322900C>ACA393086036HCN4c.3193G>T (p.Val1065Phe)
c.1975G>T (p.Val659Phe)
 gnomAD v4
15g.73322900C=CA2187186938HCN4c.3193G= (p.Val1065=)
c.1975G= (p.Val659=)
15g.73322900C>GCA393086035HCN4c.3193G>C (p.Val1065Leu)
c.1975G>C (p.Val659Leu)
 gnomAD v4
15g.73322900C>TCA393086034HCN4c.3193G>A (p.Val1065Ile)
c.1975G>A (p.Val659Ile)
 ClinVar dbSNP gnomAD v4
15g.73322901C>ACA393086037HCN4c.3192G>T (p.Gln1064His)
c.1974G>T (p.Gln658His)
 gnomAD v4
15g.73322901C=CA2187186943HCN4c.3192G= (p.Gln1064=)
c.1974G= (p.Gln658=)
15g.73322901C>GCA393086038HCN4c.3192G>C (p.Gln1064His)
c.1974G>C (p.Gln658His)
 ClinVar dbSNP gnomAD v4
15g.73322901C>TCA491477942HCN4c.3192G>A (p.Gln1064=)
c.1974G>A (p.Gln658=)
 dbSNP gnomAD v4
15g.73322905_73322920delCA2629370534HCN4c.3177_3192del (p.Ser1059ArgfsTer?)
c.1959_1974del (p.Ser653ArgfsTer?)
 gnomAD v4
15g.73322902T>ACA393086039HCN4c.3191A>T (p.Gln1064Leu)
c.1973A>T (p.Gln658Leu)
 gnomAD v4
15g.73322902T>CCA393086041HCN4c.3191A>G (p.Gln1064Arg)
c.1973A>G (p.Gln658Arg)
 gnomAD v4
15g.73322902T>GCA393086040HCN4c.3191A>C (p.Gln1064Pro)
c.1973A>C (p.Gln658Pro)
 dbSNP gnomAD v3 gnomAD v4
15g.73322902T=CA2187186945HCN4c.3191A= (p.Gln1064=)
c.1973A= (p.Gln658=)
15g.73322907_73322914delCA2629370535HCN4c.3184_3191del (p.Pro1062GlyfsTer?)
c.1966_1973del (p.Pro656GlyfsTer?)
 gnomAD v4
15g.73322903G>ACA393086042HCN4c.3190C>T (p.Gln1064Ter)
c.1972C>T (p.Gln658Ter)
 gnomAD v4
15g.73322903G>CCA393086043HCN4c.3190C>G (p.Gln1064Glu)
c.1972C>G (p.Gln658Glu)
 gnomAD v4
15g.73322903G=CA2187186950HCN4c.3190C= (p.Gln1064=)
c.1972C= (p.Gln658=)
15g.73322903G>TCA393086044HCN4c.3190C>A (p.Gln1064Lys)
c.1972C>A (p.Gln658Lys)
 gnomAD v4
15g.73322904_73322906dupCA2804714144HCN4c.3188_3190dup (p.Pro1063_Gln1064insPro)
c.1970_1972dup (p.Pro657_Gln658insPro)
15g.73322906delCA2575783820HCN4c.3190del (p.Gln1064ArgfsTer?)
c.1972del (p.Gln658ArgfsTer?)
 gnomAD v4
15g.73322904G>ACA491477944HCN4c.3189C>T (p.Pro1063=)
c.1971C>T (p.Pro657=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73322904G>CCA491477945HCN4c.3189C>G (p.Pro1063=)
c.1971C>G (p.Pro657=)
15g.73322904G=CA2187186953HCN4c.3189C= (p.Pro1063=)
c.1971C= (p.Pro657=)
15g.73322904G>TCA491477946HCN4c.3189C>A (p.Pro1063=)
c.1971C>A (p.Pro657=)
 dbSNP gnomAD v2 gnomAD v4
15g.73322904_73322924dupCA619410586HCN4c.3169_3189dup (p.Pro1063_Gln1064insAlaSerSerProProProPro)
c.1951_1971dup (p.Pro657_Gln658insAlaSerSerProProProPro)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73322905G>ACA393086045HCN4c.3188C>T (p.Pro1063Leu)
c.1970C>T (p.Pro657Leu)
 gnomAD v4
15g.73322905G>CCA393086046HCN4c.3188C>G (p.Pro1063Arg)
c.1970C>G (p.Pro657Arg)
 gnomAD v4
15g.73322905G=CA2187186957HCN4c.3188C= (p.Pro1063=)
c.1970C= (p.Pro657=)
15g.73322905G>TCA393086047HCN4c.3188C>A (p.Pro1063His)
c.1970C>A (p.Pro657His)
 dbSNP gnomAD v4
15g.73322906G>ACA393086048HCN4c.3187C>T (p.Pro1063Ser)
c.1969C>T (p.Pro657Ser)
 ClinVar gnomAD v4
15g.73322906G>CCA393086049HCN4c.3187C>G (p.Pro1063Ala)
c.1969C>G (p.Pro657Ala)
15g.73322906G=CA2187186960HCN4c.3187C= (p.Pro1063=)
c.1969C= (p.Pro657=)
15g.73322906G>TCA7648874HCN4c.3187C>A (p.Pro1063Thr)
c.1969C>A (p.Pro657Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322907T>ACA491477949HCN4c.3186A>T (p.Pro1062=)
c.1968A>T (p.Pro656=)
15g.73322907T>CCA491477950HCN4c.3186A>G (p.Pro1062=)
c.1968A>G (p.Pro656=)
 ClinVar gnomAD v4
15g.73322907T>GCA491477948HCN4c.3186A>C (p.Pro1062=)
c.1968A>C (p.Pro656=)
 dbSNP gnomAD v3 gnomAD v4
15g.73322907T=CA2187186963HCN4c.3186A= (p.Pro1062=)
c.1968A= (p.Pro656=)
15g.73322910_73322920delCA2629370536HCN4c.3176_3186del (p.Ser1059ThrfsTer?)
c.1958_1968del (p.Ser653ThrfsTer?)
 gnomAD v4
15g.73322908G>ACA393086050HCN4c.3185C>T (p.Pro1062Leu)
c.1967C>T (p.Pro656Leu)
 dbSNP gnomAD v2 gnomAD v4
15g.73322908G>CCA393086051HCN4c.3185C>G (p.Pro1062Arg)
c.1967C>G (p.Pro656Arg)
15g.73322908G=CA2187186965HCN4c.3185C= (p.Pro1062=)
c.1967C= (p.Pro656=)
15g.73322908G>TCA393086052HCN4c.3185C>A (p.Pro1062Gln)
c.1967C>A (p.Pro656Gln)
 gnomAD v4
15g.73322909delCA2575783821HCN4c.3185del (p.Pro1062HisfsTer?)
c.1967del (p.Pro656HisfsTer?)
15g.73322913_73322930delCA2629370537HCN4c.3168_3185del (p.Ala1057_Pro1062del)
c.1950_1967del (p.Ala651_Pro656del)
 gnomAD v4
15g.73322909G>ACA393086055HCN4c.3184C>T (p.Pro1062Ser)
c.1966C>T (p.Pro656Ser)
 ClinVar dbSNP gnomAD v4
15g.73322909G>CCA393086053HCN4c.3184C>G (p.Pro1062Ala)
c.1966C>G (p.Pro656Ala)
 ClinVar
15g.73322909G=CA2187186968HCN4c.3184C= (p.Pro1062=)
c.1966C= (p.Pro656=)
15g.73322909G>TCA393086054HCN4c.3184C>A (p.Pro1062Thr)
c.1966C>A (p.Pro656Thr)
 ClinVar gnomAD v4
15g.73322910T>ACA491477953HCN4c.3183A>T (p.Pro1061=)
c.1965A>T (p.Pro655=)
15g.73322910T>CCA491477957HCN4c.3183A>G (p.Pro1061=)
c.1965A>G (p.Pro655=)
 dbSNP gnomAD v2 gnomAD v4
15g.73322910T>GCA491477955HCN4c.3183A>C (p.Pro1061=)
c.1965A>C (p.Pro655=)
 dbSNP gnomAD v3 gnomAD v4
15g.73322910T=CA2187186970HCN4c.3183A= (p.Pro1061=)
c.1965A= (p.Pro655=)

Number of alleles fetched