Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.169540947_169541054delCA2746577665F5c.4052_4159del (p.Ala1351_Pro1386del)
c.4067_4174del (p.Ala1356_Pro1391del)
c.3641_3748del (p.Ala1214_Pro1249del)
1g.169540947_169541055delinsCTGACTGAGTTCTGGAGAGAGGTTTGTCTGGCTGAGGTCTAGAGAAAGGGTTGTATGGCTGGGGTCTGGAGAAAGGGGCATCTGACCGAGGGCTGGGGAAAGGTTTGTTCA1206140002F5c.4035_4143delinsAACAAACCTTTCCCCAGCCCTCGGTCAGATGCCCCTTTCTCCAGACCCCAGCCATACAACCCTTTCTCTAGACCTCAGCCAGACAAACCTCTCTCCAGAACTCAGTCAG (p.Gln1345=)
c.4050_4158delinsAACAAACCTTTCCCCAGCCCTCGGTCAGATGCCCCTTTCTCCAGACCCCAGCCATACAACCCTTTCTCTAGACCTCAGCCAGACAAACCTCTCTCCAGAACTCAGTCAG (p.Gln1350=)
c.3624_3732delinsAACAAACCTTTCCCCAGCCCTCGGTCAGATGCCCCTTTCTCCAGACCCCAGCCATACAACCCTTTCTCTAGACCTCAGCCAGACAAACCTCTCTCCAGAACTCAGTCAG (p.Gln1208=)
1g.169540982_169541089delCA1233749F5c.4035_4142del (p.Thr1346_Gln1381del)
c.4050_4157del (p.Thr1351_Gln1386del)
c.3624_3731del (p.Thr1209_Gln1244del)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.169540982_169541090delinsGGTCTAGAGAAAGGGTTGTATGGCTGGGGTCTGGAGAAAGGGGCATCTGACCGAGGGCTGGGGAAAGGTTTGTTTGACTGAGTTCTGGAGAGAGGTTTGTCTGGCTGAACA1206140016F5c.4000_4108delinsTTCAGCCAGACAAACCTCTCTCCAGAACTCAGTCAAACAAACCTTTCCCCAGCCCTCGGTCAGATGCCCCTTTCTCCAGACCCCAGCCATACAACCCTTTCTCTAGACC (p.Phe1334=)
c.4015_4123delinsTTCAGCCAGACAAACCTCTCTCCAGAACTCAGTCAAACAAACCTTTCCCCAGCCCTCGGTCAGATGCCCCTTTCTCCAGACCCCAGCCATACAACCCTTTCTCTAGACC (p.Phe1339=)
c.3589_3697delinsTTCAGCCAGACAAACCTCTCTCCAGAACTCAGTCAAACAAACCTTTCCCCAGCCCTCGGTCAGATGCCCCTTTCTCCAGACCCCAGCCATACAACCCTTTCTCTAGACC (p.Phe1197=)
1g.169541008_169541115delCA1233755F5c.4000_4107del (p.Phe1334_Asp1369del)
c.4015_4122del (p.Phe1339_Asp1374del)
c.3589_3696del (p.Phe1197_Asp1232del)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.169541054_169541055insCTGACTGAGTTCTGGAGAGAGGTTTGTCTGGCTGAGGTCTAGAGAAAGAGTTGTATGGCTGGGGTCTGGAGAAAGGGGCATCTGACCGAGGGCTGGGGAAAGGTTTGTCA1008977749F5c.4094_4095insTCTTTCTCTAGACCTCAGCCAGACAAACCTCTCTCCAGAACTCAGTCAGACAAACCTTTCCCCAGCCCTCGGTCAGATGCCCCTTTCTCCAGACCCCAGCCATACAAC (p.Thr1365_Leu1366insLeuSerLeuAspLeuSerGlnThrAsnLeuSerProGluLeuSerGlnThrAsnLeuSerProAlaLeuGlyGlnMetProLeuSerProAspProSerHisThrThr)
c.4109_4110insTCTTTCTCTAGACCTCAGCCAGACAAACCTCTCTCCAGAACTCAGTCAGACAAACCTTTCCCCAGCCCTCGGTCAGATGCCCCTTTCTCCAGACCCCAGCCATACAAC (p.Thr1370_Leu1371insLeuSerLeuAspLeuSerGlnThrAsnLeuSerProGluLeuSerGlnThrAsnLeuSerProAlaLeuGlyGlnMetProLeuSerProAspProSerHisThrThr)
c.3683_3684insTCTTTCTCTAGACCTCAGCCAGACAAACCTCTCTCCAGAACTCAGTCAGACAAACCTTTCCCCAGCCCTCGGTCAGATGCCCCTTTCTCCAGACCCCAGCCATACAAC (p.Thr1228_Leu1229insLeuSerLeuAspLeuSerGlnThrAsnLeuSerProGluLeuSerGlnThrAsnLeuSerProAlaLeuGlyGlnMetProLeuSerProAspProSerHisThrThr)
dbSNP gnomAD v3 gnomAD v4
1g.169541008_169541116delinsGGGTCTGGAGAAAGGGGCATCTGACCGAGGGCTGGGGAAAGGTTTGTTTGACTGAGTTCTGGAGAGAGGTTTGTCTGGCTGAAGTCTAGAGAAAGGGTTGTATGGCTGACA1206140029F5c.3974_4082delinsTCAGCCATACAACCCTTTCTCTAGACTTCAGCCAGACAAACCTCTCTCCAGAACTCAGTCAAACAAACCTTTCCCCAGCCCTCGGTCAGATGCCCCTTTCTCCAGACCC (p.Leu1325=)
c.3989_4097delinsTCAGCCATACAACCCTTTCTCTAGACTTCAGCCAGACAAACCTCTCTCCAGAACTCAGTCAAACAAACCTTTCCCCAGCCCTCGGTCAGATGCCCCTTTCTCCAGACCC (p.Leu1330=)
c.3563_3671delinsTCAGCCATACAACCCTTTCTCTAGACTTCAGCCAGACAAACCTCTCTCCAGAACTCAGTCAAACAAACCTTTCCCCAGCCCTCGGTCAGATGCCCCTTTCTCCAGACCC (p.Leu1188=)
1g.169541021_169541128delCA1008977761F5c.3974_4081del (p.Leu1325_Asp1360del)
c.3989_4096del (p.Leu1330_Asp1365del)
c.3563_3670del (p.Leu1188_Asp1223del)
dbSNP gnomAD v3 gnomAD v4
1g.169541013T>ACA421930070F5c.4077A>T (p.Pro1359=)
c.4092A>T (p.Pro1364=)
c.3666A>T (p.Pro1222=)
1g.169541013T>CCA421930068F5c.4077A>G (p.Pro1359=)
c.4092A>G (p.Pro1364=)
c.3666A>G (p.Pro1222=)
1g.169541013T>GCA421930067F5c.4077A>C (p.Pro1359=)
c.4092A>C (p.Pro1364=)
c.3666A>C (p.Pro1222=)
1g.169541014G>ACA343145736F5c.4076C>T (p.Pro1359Leu)
c.4091C>T (p.Pro1364Leu)
c.3665C>T (p.Pro1222Leu)
1g.169541014G>CCA343145738F5c.4076C>G (p.Pro1359Arg)
c.4091C>G (p.Pro1364Arg)
c.3665C>G (p.Pro1222Arg)
1g.169541014G>TCA343145740F5c.4076C>A (p.Pro1359Gln)
c.4091C>A (p.Pro1364Gln)
c.3665C>A (p.Pro1222Gln)
1g.169541015G>ACA343145742F5c.4075C>T (p.Pro1359Ser)
c.4090C>T (p.Pro1364Ser)
c.3664C>T (p.Pro1222Ser)
dbSNP gnomAD v2 gnomAD v4 COSMIC
1g.169541015G>CCA343145745F5c.4075C>G (p.Pro1359Ala)
c.4090C>G (p.Pro1364Ala)
c.3664C>G (p.Pro1222Ala)
dbSNP gnomAD v2 gnomAD v4
1g.169541015G=CA1206140032F5c.4075C= (p.Pro1359=)
c.4090C= (p.Pro1364=)
c.3664C= (p.Pro1222=)
1g.169541015G>TCA343145747F5c.4075C>A (p.Pro1359Thr)
c.4090C>A (p.Pro1364Thr)
c.3664C>A (p.Pro1222Thr)
1g.169541016A>CCA421930073F5c.4074T>G (p.Ser1358=)
c.4089T>G (p.Ser1363=)
c.3663T>G (p.Ser1221=)
1g.169541016A>GCA421930077F5c.4074T>C (p.Ser1358=)
c.4089T>C (p.Ser1363=)
c.3663T>C (p.Ser1221=)
1g.169541016A>TCA421930075F5c.4074T>A (p.Ser1358=)
c.4089T>A (p.Ser1363=)
c.3663T>A (p.Ser1221=)
1g.169541017G>ACA343145758F5c.4073C>T (p.Ser1358Phe)
c.4088C>T (p.Ser1363Phe)
c.3662C>T (p.Ser1221Phe)
1g.169541017G>CCA343145760F5c.4073C>G (p.Ser1358Cys)
c.4088C>G (p.Ser1363Cys)
c.3662C>G (p.Ser1221Cys)
1g.169541017G=CA1206140033F5c.4073C= (p.Ser1358=)
c.4088C= (p.Ser1363=)
c.3662C= (p.Ser1221=)
1g.169541017G>TCA343145769F5c.4073C>A (p.Ser1358Tyr)
c.4088C>A (p.Ser1363Tyr)
c.3662C>A (p.Ser1221Tyr)
dbSNP gnomAD v2 gnomAD v4
1g.169541018A>CCA343145770F5c.4072T>G (p.Ser1358Ala)
c.4087T>G (p.Ser1363Ala)
c.3661T>G (p.Ser1221Ala)
1g.169541018A>GCA343145771F5c.4072T>C (p.Ser1358Pro)
c.4087T>C (p.Ser1363Pro)
c.3661T>C (p.Ser1221Pro)
ClinVar gnomAD v4
1g.169541018A>TCA343145772F5c.4072T>A (p.Ser1358Thr)
c.4087T>A (p.Ser1363Thr)
c.3661T>A (p.Ser1221Thr)
1g.169541019A>CCA421930088F5c.4071T>G (p.Leu1357=)
c.4086T>G (p.Leu1362=)
c.3660T>G (p.Leu1220=)
1g.169541019A>GCA421930089F5c.4071T>C (p.Leu1357=)
c.4086T>C (p.Leu1362=)
c.3660T>C (p.Leu1220=)
gnomAD v3 gnomAD v4
1g.169541019A>TCA421930090F5c.4071T>A (p.Leu1357=)
c.4086T>A (p.Leu1362=)
c.3660T>A (p.Leu1220=)
1g.169541020A>CCA343145780F5c.4070T>G (p.Leu1357Arg)
c.4085T>G (p.Leu1362Arg)
c.3659T>G (p.Leu1220Arg)
1g.169541020A>GCA343145776F5c.4070T>C (p.Leu1357Pro)
c.4085T>C (p.Leu1362Pro)
c.3659T>C (p.Leu1220Pro)
1g.169541020A>TCA343145778F5c.4070T>A (p.Leu1357His)
c.4085T>A (p.Leu1362His)
c.3659T>A (p.Leu1220His)
1g.169541021G>ACA343145781F5c.4069C>T (p.Leu1357Phe)
c.4084C>T (p.Leu1362Phe)
c.3658C>T (p.Leu1220Phe)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.169541021G>CCA343145782F5c.4069C>G (p.Leu1357Val)
c.4084C>G (p.Leu1362Val)
c.3658C>G (p.Leu1220Val)
dbSNP gnomAD v3 gnomAD v4
1g.169541021G=CA1206140035F5c.4069C= (p.Leu1357=)
c.4084C= (p.Leu1362=)
c.3658C= (p.Leu1220=)
1g.169541021G>TCA343145783F5c.4069C>A (p.Leu1357Ile)
c.4084C>A (p.Leu1362Ile)
c.3658C>A (p.Leu1220Ile)
dbSNP gnomAD v3 gnomAD v4 COSMIC
1g.169541021_169541129delinsGGGGCATCTGACCGAGGGCTGGGGAAAGGTTTGTTTGACTGAGTTCTGGAGAGAGGTTTGTCTGGCTGAAGTCTAGAGAAAGGGTTGTATGGCTGAGGTCTGGAGAAATCA1206140034F5c.3961_4069delinsATTTCTCCAGACCTCAGCCATACAACCCTTTCTCTAGACTTCAGCCAGACAAACCTCTCTCCAGAACTCAGTCAAACAAACCTTTCCCCAGCCCTCGGTCAGATGCCCC (p.Ile1321=)
c.3976_4084delinsATTTCTCCAGACCTCAGCCATACAACCCTTTCTCTAGACTTCAGCCAGACAAACCTCTCTCCAGAACTCAGTCAAACAAACCTTTCCCCAGCCCTCGGTCAGATGCCCC (p.Ile1326=)
c.3550_3658delinsATTTCTCCAGACCTCAGCCATACAACCCTTTCTCTAGACTTCAGCCAGACAAACCTCTCTCCAGAACTCAGTCAAACAAACCTTTCCCCAGCCCTCGGTCAGATGCCCC (p.Ile1184=)
1g.169541022G>ACA1233765F5c.4068C>T (p.Pro1356=)
c.4083C>T (p.Pro1361=)
c.3657C>T (p.Pro1219=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.169541022G>CCA421930099F5c.4068C>G (p.Pro1356=)
c.4083C>G (p.Pro1361=)
c.3657C>G (p.Pro1219=)
1g.169541022G=CA1206140036F5c.4068C= (p.Pro1356=)
c.4083C= (p.Pro1361=)
c.3657C= (p.Pro1219=)
1g.169541022G>TCA421930103F5c.4068C>A (p.Pro1356=)
c.4083C>A (p.Pro1361=)
c.3657C>A (p.Pro1219=)
1g.169541055_169541162delCA1233764F5c.3961_4068del (p.Ile1321_Pro1356del)
c.3976_4083del (p.Ile1326_Pro1361del)
c.3550_3657del (p.Ile1184_Pro1219del)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.169541023G>ACA343145790F5c.4067C>T (p.Pro1356Leu)
c.4082C>T (p.Pro1361Leu)
c.3656C>T (p.Pro1219Leu)
dbSNP
1g.169541023G>CCA343145792F5c.4067C>G (p.Pro1356Arg)
c.4082C>G (p.Pro1361Arg)
c.3656C>G (p.Pro1219Arg)
1g.169541023G=CA1206140037F5c.4067C= (p.Pro1356=)
c.4082C= (p.Pro1361=)
c.3656C= (p.Pro1219=)
1g.169541023G>TCA343145794F5c.4067C>A (p.Pro1356His)
c.4082C>A (p.Pro1361His)
c.3656C>A (p.Pro1219His)
1g.169541024G>ACA343145798F5c.4066C>T (p.Pro1356Ser)
c.4081C>T (p.Pro1361Ser)
c.3655C>T (p.Pro1219Ser)
dbSNP gnomAD v2 gnomAD v4
1g.169541024G>CCA343145800F5c.4066C>G (p.Pro1356Ala)
c.4081C>G (p.Pro1361Ala)
c.3655C>G (p.Pro1219Ala)
gnomAD v4

Number of alleles fetched