Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.132327369C>ACA375326897SETXc.4229G>T (p.Arg1410Ile)
n.4413G>T
9g.132327369C=CA1882147311SETXc.4229G= (p.Arg1410=)
n.4413G=
9g.132327369C>GCA375326899SETXc.4229G>C (p.Arg1410Thr)
n.4413G>C
dbSNP
9g.132327369C>TCA375326900SETXc.4229G>A (p.Arg1410Lys)
n.4413G>A
9g.132327370T>ACA375326902SETXc.4228A>T (p.Arg1410Ter)
n.4412A>T
9g.132327370T>CCA375326903SETXc.4228A>G (p.Arg1410Gly)
n.4412A>G
dbSNP gnomAD v4
9g.132327370T>GCA467807737SETXc.4228A>C (p.Arg1410=)
n.4412A>C
9g.132327370T=CA1882147312SETXc.4228A= (p.Arg1410=)
n.4412A=
9g.132327371G>ACA467807738SETXc.4227C>T (p.Asn1409=)
n.4411C>T
gnomAD v4
9g.132327371G>CCA375326905SETXc.4227C>G (p.Asn1409Lys)
n.4411C>G
gnomAD v4
9g.132327371G>TCA375326907SETXc.4227C>A (p.Asn1409Lys)
n.4411C>A
9g.132327372T>ACA375326909SETXc.4226A>T (p.Asn1409Ile)
n.4410A>T
9g.132327372T>CCA375326910SETXc.4226A>G (p.Asn1409Ser)
n.4410A>G
9g.132327372T>GCA375326912SETXc.4226A>C (p.Asn1409Thr)
n.4410A>C
9g.132327373T>ACA233099SETXc.4225A>T (p.Asn1409Tyr)
n.4409A>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.132327373T>CCA5297242SETXc.4225A>G (p.Asn1409Asp)
n.4409A>G
dbSNP ExAC gnomAD v2 gnomAD v4
9g.132327373T>GCA375326915SETXc.4225A>C (p.Asn1409His)
n.4409A>C
9g.132327373T=CA1882147313SETXc.4225A= (p.Asn1409=)
n.4409A=
9g.132327374A>CCA375326917SETXc.4224T>G (p.Ser1408Arg)
n.4408T>G
9g.132327374A>GCA467807739SETXc.4224T>C (p.Ser1408=)
n.4408T>C
9g.132327374A>TCA375326919SETXc.4224T>A (p.Ser1408Arg)
n.4408T>A
9g.132327375C>ACA375326921SETXc.4223G>T (p.Ser1408Ile)
n.4407G>T
9g.132327375C=CA1882147314SETXc.4223G= (p.Ser1408=)
n.4407G=
9g.132327375C>GCA375326922SETXc.4223G>C (p.Ser1408Thr)
n.4407G>C
dbSNP
9g.132327375C>TCA375326924SETXc.4223G>A (p.Ser1408Asn)
n.4407G>A
9g.132327376T>ACA375326928SETXc.4222A>T (p.Ser1408Cys)
n.4406A>T
9g.132327376T>CCA200807217SETXc.4222A>G (p.Ser1408Gly)
n.4406A>G
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.132327376T>GCA375326927SETXc.4222A>C (p.Ser1408Arg)
n.4406A>C
dbSNP gnomAD v4
9g.132327376T=CA1882147315SETXc.4222A= (p.Ser1408=)
n.4406A=
9g.132327377G>ACA467807740SETXc.4221C>T (p.Asn1407=)
n.4405C>T
9g.132327377G>CCA375326929SETXc.4221C>G (p.Asn1407Lys)
n.4405C>G
9g.132327377G>TCA375326931SETXc.4221C>A (p.Asn1407Lys)
n.4405C>A
gnomAD v4
9g.132327378T>ACA375326933SETXc.4220A>T (p.Asn1407Ile)
n.4404A>T
9g.132327378T>CCA5297243SETXc.4220A>G (p.Asn1407Ser)
n.4404A>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.132327378T>GCA375326935SETXc.4220A>C (p.Asn1407Thr)
n.4404A>C
9g.132327378T=CA1882147316SETXc.4220A= (p.Asn1407=)
n.4404A=
9g.132327379T>ACA375326937SETXc.4219A>T (p.Asn1407Tyr)
n.4403A>T
9g.132327379T>CCA375326938SETXc.4219A>G (p.Asn1407Asp)
n.4403A>G
9g.132327379T>GCA375326939SETXc.4219A>C (p.Asn1407His)
n.4403A>C
9g.132327380G>ACA467807741SETXc.4218C>T (p.Ala1406=)
n.4402C>T
9g.132327380G>CCA467807742SETXc.4218C>G (p.Ala1406=)
n.4402C>G
9g.132327380G>TCA467807743SETXc.4218C>A (p.Ala1406=)
n.4402C>A
9g.132327381G>ACA375326940SETXc.4217C>T (p.Ala1406Val)
n.4401C>T
9g.132327381G>CCA200807227SETXc.4217C>G (p.Ala1406Gly)
n.4401C>G
ClinVar dbSNP gnomAD v4
9g.132327381G=CA1882147317SETXc.4217C= (p.Ala1406=)
n.4401C=
9g.132327381G>TCA5297244SETXc.4217C>A (p.Ala1406Asp)
n.4401C>A
dbSNP ExAC gnomAD v2 gnomAD v4
9g.132327382C>ACA375326943SETXc.4216G>T (p.Ala1406Ser)
n.4400G>T
9g.132327382C=CA1882147318SETXc.4216G= (p.Ala1406=)
n.4400G=
9g.132327382C>GCA375326942SETXc.4216G>C (p.Ala1406Pro)
n.4400G>C
9g.132327382C>TCA5297245SETXc.4216G>A (p.Ala1406Thr)
n.4400G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.132327383A>CCA467807746SETXc.4215T>G (p.Leu1405=)
n.4399T>G
9g.132327383A>GCA467807744SETXc.4215T>C (p.Leu1405=)
n.4399T>C
dbSNP
9g.132327383A>TCA467807745SETXc.4215T>A (p.Leu1405=)
n.4399T>A
9g.132327384A>CCA375326944SETXc.4214T>G (p.Leu1405Arg)
n.4398T>G
9g.132327384A>GCA375326946SETXc.4214T>C (p.Leu1405Pro)
n.4398T>C
gnomAD v4
9g.132327384A>TCA375326945SETXc.4214T>A (p.Leu1405His)
n.4398T>A
9g.132327385G>ACA5297246SETXc.4213C>T (p.Leu1405Phe)
n.4397C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.132327385G>CCA375326948SETXc.4213C>G (p.Leu1405Val)
n.4397C>G
dbSNP
9g.132327385G=CA1882147319SETXc.4213C= (p.Leu1405=)
n.4397C=
9g.132327385G>TCA375326947SETXc.4213C>A (p.Leu1405Ile)
n.4397C>A
9g.132327386T>ACA467807747SETXc.4212A>T (p.Val1404=)
n.4396A>T
9g.132327386T>CCA467807748SETXc.4212A>G (p.Val1404=)
n.4396A>G
gnomAD v4
9g.132327386T>GCA467807749SETXc.4212A>C (p.Val1404=)
n.4396A>C
9g.132327387A>CCA375326950SETXc.4211T>G (p.Val1404Gly)
n.4395T>G
9g.132327387A>GCA375326951SETXc.4211T>C (p.Val1404Ala)
n.4395T>C
9g.132327387A>TCA375326952SETXc.4211T>A (p.Val1404Glu)
n.4395T>A
9g.132327388C>ACA375326954SETXc.4210G>T (p.Val1404Leu)
n.4394G>T
9g.132327388C=CA1882147320SETXc.4210G= (p.Val1404=)
n.4394G=
9g.132327388C>GCA375326956SETXc.4210G>C (p.Val1404Leu)
n.4394G>C
9g.132327388C>TCA375326957SETXc.4210G>A (p.Val1404Ile)
n.4394G>A
ClinVar dbSNP gnomAD v4
9g.132327389C>ACA375326958SETXc.4209G>T (p.Glu1403Asp)
n.4393G>T
9g.132327389C=CA1882147321SETXc.4209G= (p.Glu1403=)
n.4393G=
9g.132327389C>GCA375326961SETXc.4209G>C (p.Glu1403Asp)
n.4393G>C
9g.132327389C>TCA467807750SETXc.4209G>A (p.Glu1403=)
n.4393G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.132327389_132327390insAACAAATGAAGTAACA918568264SETXc.4208_4209insTTACTTCATTTGTT (p.Glu1403AspfsTer16)
n.4392_4393insTTACTTCATTTGTT
dbSNP
9g.132327390T>ACA375326963SETXc.4208A>T (p.Glu1403Val)
n.4392A>T
9g.132327390T>CCA375326964SETXc.4208A>G (p.Glu1403Gly)
n.4392A>G
9g.132327390T>GCA375326966SETXc.4208A>C (p.Glu1403Ala)
n.4392A>C
9g.132327391C>ACA375326968SETXc.4207G>T (p.Glu1403Ter)
n.4391G>T
9g.132327391C>GCA375326970SETXc.4207G>C (p.Glu1403Gln)
n.4391G>C
9g.132327391C>TCA375326969SETXc.4207G>A (p.Glu1403Lys)
n.4391G>A
9g.132327392A>CCA467807751SETXc.4206T>G (p.Thr1402=)
n.4390T>G
9g.132327392A>GCA467807752SETXc.4206T>C (p.Thr1402=)
n.4390T>C
9g.132327392A>TCA467807753SETXc.4206T>A (p.Thr1402=)
n.4390T>A
9g.132327393G>ACA375326973SETXc.4205C>T (p.Thr1402Ile)
n.4389C>T
dbSNP gnomAD v4
9g.132327393G>CCA375326975SETXc.4205C>G (p.Thr1402Ser)
n.4389C>G
9g.132327393G>TCA375326976SETXc.4205C>A (p.Thr1402Asn)
n.4389C>A
9g.132327394T>ACA5297247SETXc.4204A>T (p.Thr1402Ser)
n.4388A>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.132327394T>CCA375326979SETXc.4204A>G (p.Thr1402Ala)
n.4388A>G
9g.132327394T>GCA375326982SETXc.4204A>C (p.Thr1402Pro)
n.4388A>C
9g.132327394T=CA1882147322SETXc.4204A= (p.Thr1402=)
n.4388A=
9g.132327395T>ACA467807754SETXc.4203A>T (p.Gly1401=)
n.4387A>T
9g.132327395T>CCA467807756SETXc.4203A>G (p.Gly1401=)
n.4387A>G
9g.132327395T>GCA467807755SETXc.4203A>C (p.Gly1401=)
n.4387A>C
gnomAD v4
9g.132327396C>ACA5297248SETXc.4202G>T (p.Gly1401Val)
n.4386G>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.132327396C=CA1882147323SETXc.4202G= (p.Gly1401=)
n.4386G=
9g.132327396C>GCA375326984SETXc.4202G>C (p.Gly1401Ala)
n.4386G>C
9g.132327396C>TCA375326985SETXc.4202G>A (p.Gly1401Glu)
n.4386G>A
9g.132327397C>ACA375326987SETXc.4201G>T (p.Gly1401Ter)
n.4385G>T
9g.132327397C>GCA375326988SETXc.4201G>C (p.Gly1401Arg)
n.4385G>C
9g.132327397C>TCA375326986SETXc.4201G>A (p.Gly1401Arg)
n.4385G>A
9g.132327398T>ACA467807757SETXc.4200A>T (p.Gly1400=)
n.4384A>T
9g.132327398T>CCA467807758SETXc.4200A>G (p.Gly1400=)
n.4384A>G
9g.132327398T>GCA5297249SETXc.4200A>C (p.Gly1400=)
n.4384A>C
dbSNP ExAC gnomAD v2 gnomAD v4
9g.132327398T=CA1882147324SETXc.4200A= (p.Gly1400=)
n.4384A=
9g.132327399C>ACA375326990SETXc.4199G>T (p.Gly1400Val)
n.4383G>T
dbSNP gnomAD v3 gnomAD v4
9g.132327399C=CA1882147325SETXc.4199G= (p.Gly1400=)
n.4383G=
9g.132327399C>GCA375326991SETXc.4199G>C (p.Gly1400Ala)
n.4383G>C
9g.132327399C>TCA375326993SETXc.4199G>A (p.Gly1400Glu)
n.4383G>A
9g.132327400C>ACA375326995SETXc.4198G>T (p.Gly1400Ter)
n.4382G>T
9g.132327400C>GCA375326996SETXc.4198G>C (p.Gly1400Arg)
n.4382G>C
9g.132327400C>TCA375326998SETXc.4198G>A (p.Gly1400Arg)
n.4382G>A
gnomAD v4
9g.132327401T>ACA467807759SETXc.4197A>T (p.Thr1399=)
n.4381A>T
9g.132327401T>CCA5297250SETXc.4197A>G (p.Thr1399=)
n.4381A>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.132327401T>GCA467807760SETXc.4197A>C (p.Thr1399=)
n.4381A>C
9g.132327401T=CA1882147326SETXc.4197A= (p.Thr1399=)
n.4381A=
9g.132327402G>ACA375327000SETXc.4196C>T (p.Thr1399Ile)
n.4380C>T
dbSNP gnomAD v2 gnomAD v4
9g.132327402G>CCA375327002SETXc.4196C>G (p.Thr1399Arg)
n.4380C>G
9g.132327402G=CA1882147327SETXc.4196C= (p.Thr1399=)
n.4380C=
9g.132327402G>TCA375327003SETXc.4196C>A (p.Thr1399Lys)
n.4380C>A
9g.132327402_132327404delCA2692256381SETXc.4194_4196del (p.Cys1398Ter)
n.4378_4380del
gnomAD v4
9g.132327403T>ACA375327005SETXc.4195A>T (p.Thr1399Ser)
n.4379A>T
9g.132327403T>CCA375327006SETXc.4195A>G (p.Thr1399Ala)
n.4379A>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.132327403T>GCA375327004SETXc.4195A>C (p.Thr1399Pro)
n.4379A>C
9g.132327403T=CA1882147328SETXc.4195A= (p.Thr1399=)
n.4379A=
9g.132327404A=CA1882147329SETXc.4194T= (p.Cys1398=)
n.4378T=
9g.132327404A>CCA375327007SETXc.4194T>G (p.Cys1398Trp)
n.4378T>G
dbSNP
9g.132327404A>GCA5297251SETXc.4194T>C (p.Cys1398=)
n.4378T>C
dbSNP ExAC gnomAD v4
9g.132327404A>TCA375327009SETXc.4194T>A (p.Cys1398Ter)
n.4378T>A
9g.132327405C>ACA5297252SETXc.4193G>T (p.Cys1398Phe)
n.4377G>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.132327405C=CA1882147330SETXc.4193G= (p.Cys1398=)
n.4377G=
9g.132327405C>GCA375327011SETXc.4193G>C (p.Cys1398Ser)
n.4377G>C
9g.132327405C>TCA375327013SETXc.4193G>A (p.Cys1398Tyr)
n.4377G>A
dbSNP
9g.132327406A=CA1882147331SETXc.4192T= (p.Cys1398=)
n.4376T=
9g.132327406A>CCA375327015SETXc.4192T>G (p.Cys1398Gly)
n.4376T>G
9g.132327406A>GCA375327018SETXc.4192T>C (p.Cys1398Arg)
n.4376T>C
9g.132327406A>TCA375327017SETXc.4192T>A (p.Cys1398Ser)
n.4376T>A
dbSNP gnomAD v2
9g.132327407_132327410dupCA2692256382SETXc.4189_4192dup (p.Cys1398Ter)
n.4373_4376dup
gnomAD v4
9g.132327407A=CA1882147332SETXc.4191T= (p.Asn1397=)
n.4375T=
9g.132327407A>CCA375327020SETXc.4191T>G (p.Asn1397Lys)
n.4375T>G
9g.132327407A>GCA467807761SETXc.4191T>C (p.Asn1397=)
n.4375T>C
dbSNP gnomAD v2 gnomAD v4
9g.132327407A>TCA375327022SETXc.4191T>A (p.Asn1397Lys)
n.4375T>A
9g.132327408T>ACA375327024SETXc.4190A>T (p.Asn1397Ile)
n.4374A>T
9g.132327408T>CCA375327025SETXc.4190A>G (p.Asn1397Ser)
n.4374A>G
9g.132327408T>GCA375327026SETXc.4190A>C (p.Asn1397Thr)
n.4374A>C
9g.132327409T>ACA375327030SETXc.4189A>T (p.Asn1397Tyr)
n.4373A>T
9g.132327409T>CCA5297253SETXc.4189A>G (p.Asn1397Asp)
n.4373A>G
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC
9g.132327409T>GCA375327029SETXc.4189A>C (p.Asn1397His)
n.4373A>C
9g.132327409T=CA1882147333SETXc.4189A= (p.Asn1397=)
n.4373A=
9g.132327410A>CCA375327035SETXc.4188T>G (p.Tyr1396Ter)
n.4372T>G
9g.132327410A>GCA467806892SETXc.4188T>C (p.Tyr1396=)
n.4372T>C
gnomAD v4
9g.132327410A>TCA375327033SETXc.4188T>A (p.Tyr1396Ter)
n.4372T>A
9g.132327411T>ACA375327036SETXc.4187A>T (p.Tyr1396Phe)
n.4371A>T
9g.132327411T>CCA375327038SETXc.4187A>G (p.Tyr1396Cys)
n.4371A>G
ClinVar dbSNP gnomAD v4
9g.132327411T>GCA375327040SETXc.4187A>C (p.Tyr1396Ser)
n.4371A>C
9g.132327411T=CA1882147334SETXc.4187A= (p.Tyr1396=)
n.4371A=
9g.132327412A=CA1882147335SETXc.4186T= (p.Tyr1396=)
n.4370T=
9g.132327412A>CCA375327041SETXc.4186T>G (p.Tyr1396Asp)
n.4370T>G
dbSNP gnomAD v4
9g.132327412A>GCA375327043SETXc.4186T>C (p.Tyr1396His)
n.4370T>C
9g.132327412A>TCA375327045SETXc.4186T>A (p.Tyr1396Asn)
n.4370T>A
gnomAD v4
9g.132327413A>CCA375327046SETXc.4185T>G (p.Asp1395Glu)
n.4369T>G
9g.132327413A>GCA467806895SETXc.4185T>C (p.Asp1395=)
n.4369T>C
9g.132327413A>TCA375327047SETXc.4185T>A (p.Asp1395Glu)
n.4369T>A
9g.132327414T>ACA200807279SETXc.4184A>T (p.Asp1395Val)
n.4368A>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.132327414T>CCA5297254SETXc.4184A>G (p.Asp1395Gly)
n.4368A>G
dbSNP ExAC gnomAD v2 gnomAD v4
9g.132327414T>GCA375327051SETXc.4184A>C (p.Asp1395Ala)
n.4368A>C
9g.132327414T=CA1882147336SETXc.4184A= (p.Asp1395=)
n.4368A=
9g.132327415C>ACA375327055SETXc.4183G>T (p.Asp1395Tyr)
n.4367G>T
9g.132327415C>GCA375327057SETXc.4183G>C (p.Asp1395His)
n.4367G>C
9g.132327415C>TCA375327053SETXc.4183G>A (p.Asp1395Asn)
n.4367G>A
gnomAD v4
9g.132327416T>ACA467806896SETXc.4182A>T (p.Ser1394=)
n.4366A>T
9g.132327416T>CCA5297255SETXc.4182A>G (p.Ser1394=)
n.4366A>G
dbSNP ExAC gnomAD v2 gnomAD v4
9g.132327416T>GCA467806897SETXc.4182A>C (p.Ser1394=)
n.4366A>C
9g.132327416T=CA1882147337SETXc.4182A= (p.Ser1394=)
n.4366A=
9g.132327417G>ACA375327059SETXc.4181C>T (p.Ser1394Leu)
n.4365C>T
ClinVar COSMIC COSMIC
9g.132327417G>CCA375327060SETXc.4181C>G (p.Ser1394Ter)
n.4365C>G
gnomAD v4
9g.132327417G>TCA375327062SETXc.4181C>A (p.Ser1394Ter)
n.4365C>A
9g.132327418A=CA1882147338SETXc.4180T= (p.Ser1394=)
n.4364T=
9g.132327418A>CCA375327065SETXc.4180T>G (p.Ser1394Ala)
n.4364T>G
9g.132327418A>GCA5297256SETXc.4180T>C (p.Ser1394Pro)
n.4364T>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.132327418A>TCA375327063SETXc.4180T>A (p.Ser1394Thr)
n.4364T>A
9g.132327419C>ACA375327067SETXc.4179G>T (p.Arg1393Ser)
n.4363G>T
9g.132327419C=CA1882147339SETXc.4179G= (p.Arg1393=)
n.4363G=
9g.132327419C>GCA375327069SETXc.4179G>C (p.Arg1393Ser)
n.4363G>C
9g.132327419C>TCA467806898SETXc.4179G>A (p.Arg1393=)
n.4363G>A
dbSNP gnomAD v4
9g.132327420C>ACA375327071SETXc.4178G>T (p.Arg1393Met)
n.4362G>T
9g.132327420C>GCA375327074SETXc.4178G>C (p.Arg1393Thr)
n.4362G>C
9g.132327420C>TCA375327075SETXc.4178G>A (p.Arg1393Lys)
n.4362G>A
gnomAD v4
9g.132327421T>ACA375327077SETXc.4177A>T (p.Arg1393Trp)
n.4361A>T
9g.132327421T>CCA5297257SETXc.4177A>G (p.Arg1393Gly)
n.4361A>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.132327421T>GCA467806899SETXc.4177A>C (p.Arg1393=)
n.4361A>C
9g.132327421T=CA1882147340SETXc.4177A= (p.Arg1393=)
n.4361A=
9g.132327422A>CCA375327080SETXc.4176T>G (p.Asp1392Glu)
n.4360T>G
9g.132327422A>GCA467806900SETXc.4176T>C (p.Asp1392=)
n.4360T>C
9g.132327422A>TCA375327081SETXc.4176T>A (p.Asp1392Glu)
n.4360T>A
9g.132327423T>ACA375327083SETXc.4175A>T (p.Asp1392Val)
n.4359A>T
9g.132327423T>CCA375327087SETXc.4175A>G (p.Asp1392Gly)
n.4359A>G
dbSNP
9g.132327423T>GCA375327085SETXc.4175A>C (p.Asp1392Ala)
n.4359A>C
9g.132327423T=CA1882147341SETXc.4175A= (p.Asp1392=)
n.4359A=
9g.132327424_132327434dupCA2692256383SETXc.4165_4175dup (p.Arg1393GlnfsTer25)
n.4349_4359dup
gnomAD v4
9g.132327424C>ACA375327088SETXc.4174G>T (p.Asp1392Tyr)
n.4358G>T
9g.132327424C=CA1882147342SETXc.4174G= (p.Asp1392=)
n.4358G=
9g.132327424C>GCA375327089SETXc.4174G>C (p.Asp1392His)
n.4358G>C
9g.132327424C>TCA5297258SETXc.4174G>A (p.Asp1392Asn)
n.4358G>A
dbSNP ExAC gnomAD v2 gnomAD v4
9g.132327425A>CCA467806901SETXc.4173T>G (p.Ser1391=)
n.4357T>G
9g.132327425A>GCA467806902SETXc.4173T>C (p.Ser1391=)
n.4357T>C
9g.132327425A>TCA467806903SETXc.4173T>A (p.Ser1391=)
n.4357T>A
9g.132327426G>ACA375327091SETXc.4172C>T (p.Ser1391Phe)
n.4356C>T
9g.132327426G>CCA375327092SETXc.4172C>G (p.Ser1391Cys)
n.4356C>G
9g.132327426G>TCA375327094SETXc.4172C>A (p.Ser1391Tyr)
n.4356C>A
9g.132327427A>CCA375327095SETXc.4171T>G (p.Ser1391Ala)
n.4355T>G
9g.132327427A>GCA375327097SETXc.4171T>C (p.Ser1391Pro)
n.4355T>C
9g.132327427A>TCA375327098SETXc.4171T>A (p.Ser1391Thr)
n.4355T>A
9g.132327428T>ACA375327100SETXc.4170A>T (p.Glu1390Asp)
n.4354A>T
9g.132327428T>CCA467806904SETXc.4170A>G (p.Glu1390=)
n.4354A>G
9g.132327428T>GCA375327102SETXc.4170A>C (p.Glu1390Asp)
n.4354A>C
9g.132327429T>ACA375327107SETXc.4169A>T (p.Glu1390Val)
n.4353A>T
9g.132327429T>CCA375327105SETXc.4169A>G (p.Glu1390Gly)
n.4353A>G
9g.132327429T>GCA375327103SETXc.4169A>C (p.Glu1390Ala)
n.4353A>C
9g.132327430C>ACA375327109SETXc.4168G>T (p.Glu1390Ter)
n.4352G>T
9g.132327430C=CA1882147343SETXc.4168G= (p.Glu1390=)
n.4352G=
9g.132327430C>GCA375327110SETXc.4168G>C (p.Glu1390Gln)
n.4352G>C
dbSNP gnomAD v4
9g.132327430C>TCA375327111SETXc.4168G>A (p.Glu1390Lys)
n.4352G>A
9g.132327431T>ACA200807298SETXc.4167A>T (p.Pro1389=)
n.4351A>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.132327431T>CCA5297259SETXc.4167A>G (p.Pro1389=)
n.4351A>G
dbSNP ExAC gnomAD v2 gnomAD v4
9g.132327431T>GCA467806905SETXc.4167A>C (p.Pro1389=)
n.4351A>C
gnomAD v4
9g.132327431T=CA1882147344SETXc.4167A= (p.Pro1389=)
n.4351A=
9g.132327432G>ACA375327114SETXc.4166C>T (p.Pro1389Leu)
n.4350C>T
dbSNP
9g.132327432G>CCA375327116SETXc.4166C>G (p.Pro1389Arg)
n.4350C>G
9g.132327432G=CA1882147345SETXc.4166C= (p.Pro1389=)
n.4350C=
9g.132327432G>TCA375327117SETXc.4166C>A (p.Pro1389Gln)
n.4350C>A
9g.132327433G>ACA375327118SETXc.4165C>T (p.Pro1389Ser)
n.4349C>T
ClinVar dbSNP
9g.132327433G>CCA375327120SETXc.4165C>G (p.Pro1389Ala)
n.4349C>G
9g.132327433G=CA1882147346SETXc.4165C= (p.Pro1389=)
n.4349C=
9g.132327433G>TCA375327121SETXc.4165C>A (p.Pro1389Thr)
n.4349C>A
9g.132327434T>ACA467806906SETXc.4164A>T (p.Val1388=)
n.4348A>T
9g.132327434T>CCA467806908SETXc.4164A>G (p.Val1388=)
n.4348A>G
9g.132327434T>GCA467806907SETXc.4164A>C (p.Val1388=)
n.4348A>C
9g.132327435A>CCA375327123SETXc.4163T>G (p.Val1388Gly)
n.4347T>G
9g.132327435A>GCA375327125SETXc.4163T>C (p.Val1388Ala)
n.4347T>C
ClinVar gnomAD v4
9g.132327435A>TCA375327126SETXc.4163T>A (p.Val1388Glu)
n.4347T>A
9g.132327436C>ACA375327130SETXc.4162G>T (p.Val1388Leu)
n.4346G>T
9g.132327436C=CA1882147347SETXc.4162G= (p.Val1388=)
n.4346G=
9g.132327436C>GCA375327132SETXc.4162G>C (p.Val1388Leu)
n.4346G>C
9g.132327436C>TCA375327129SETXc.4162G>A (p.Val1388Ile)
n.4346G>A
dbSNP gnomAD v4 COSMIC COSMIC
9g.132327437A>CCA375327134SETXc.4161T>G (p.Phe1387Leu)
n.4345T>G
9g.132327437A>GCA467806910SETXc.4161T>C (p.Phe1387=)
n.4345T>C
9g.132327437A>TCA375327136SETXc.4161T>A (p.Phe1387Leu)
n.4345T>A
9g.132327438A>CCA375327137SETXc.4160T>G (p.Phe1387Cys)
n.4344T>G
9g.132327438A>GCA375327138SETXc.4160T>C (p.Phe1387Ser)
n.4344T>C
9g.132327438A>TCA375327139SETXc.4160T>A (p.Phe1387Tyr)
n.4344T>A
9g.132327439A=CA1882147348SETXc.4159T= (p.Phe1387=)
n.4343T=
9g.132327439A>CCA375327141SETXc.4159T>G (p.Phe1387Val)
n.4343T>G
9g.132327439A>GCA375327143SETXc.4159T>C (p.Phe1387Leu)
n.4343T>C
dbSNP gnomAD v3 gnomAD v4
9g.132327439A>TCA375327144SETXc.4159T>A (p.Phe1387Ile)
n.4343T>A
9g.132327440T>ACA467806911SETXc.4158A>T (p.Ile1386=)
n.4342A>T
9g.132327440T>CCA375327145SETXc.4158A>G (p.Ile1386Met)
n.4342A>G
9g.132327440T>GCA467806912SETXc.4158A>C (p.Ile1386=)
n.4342A>C
9g.132327441A>CCA375327146SETXc.4157T>G (p.Ile1386Arg)
n.4341T>G
9g.132327441A>GCA375327147SETXc.4157T>C (p.Ile1386Thr)
n.4341T>C
gnomAD v4
9g.132327441A>TCA375327149SETXc.4157T>A (p.Ile1386Lys)
n.4341T>A
9g.132327442T>ACA375327151SETXc.4156A>T (p.Ile1386Leu)
n.4340A>T
dbSNP gnomAD v3 gnomAD v4
9g.132327442T>CCA148719SETXc.4156A>G (p.Ile1386Val)
n.4340A>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
9g.132327442T>GCA375327154SETXc.4156A>C (p.Ile1386Leu)
n.4340A>C
dbSNP gnomAD v2 gnomAD v4
9g.132327442T=CA1882147349SETXc.4156A= (p.Ile1386=)
n.4340A=
9g.132327442_132327443insCAGAATTCTGACGTATTTGTACCAGAATCTGATAGCA2692256384SETXc.4155_4156insCTATCAGATTCTGGTACAAATACGTCAGAATTCTG (p.Ile1386LeufsTer12)
n.4339_4340insCTATCAGATTCTGGTACAAATACGTCAGAATTCTG
gnomAD v4
9g.132327443G>ACA5297260SETXc.4155C>T (p.Asp1385=)
n.4339C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
9g.132327443G>CCA375327158SETXc.4155C>G (p.Asp1385Glu)
n.4339C>G
9g.132327443G=CA1882147350SETXc.4155C= (p.Asp1385=)
n.4339C=
9g.132327443G>TCA375327156SETXc.4155C>A (p.Asp1385Glu)
n.4339C>A
9g.132327444T>ACA375327161SETXc.4154A>T (p.Asp1385Val)
n.4338A>T
9g.132327444T>CCA375327162SETXc.4154A>G (p.Asp1385Gly)
n.4338A>G
9g.132327444T>GCA375327164SETXc.4154A>C (p.Asp1385Ala)
n.4338A>C
9g.132327445C>ACA375327166SETXc.4153G>T (p.Asp1385Tyr)
n.4337G>T
9g.132327445C>GCA375327167SETXc.4153G>C (p.Asp1385His)
n.4337G>C
9g.132327445C>TCA375327169SETXc.4153G>A (p.Asp1385Asn)
n.4337G>A
9g.132327446A>CCA467806925SETXc.4152T>G (p.Ser1384=)
n.4336T>G
9g.132327446A>GCA467806926SETXc.4152T>C (p.Ser1384=)
n.4336T>C
9g.132327446A>TCA467806928SETXc.4152T>A (p.Ser1384=)
n.4336T>A
9g.132327447G>ACA5297261SETXc.4151C>T (p.Ser1384Phe)
n.4335C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.132327447G>CCA375327172SETXc.4151C>G (p.Ser1384Cys)
n.4335C>G
gnomAD v4
9g.132327447G=CA1882147351SETXc.4151C= (p.Ser1384=)
n.4335C=
9g.132327447G>TCA375327173SETXc.4151C>A (p.Ser1384Tyr)
n.4335C>A
9g.132327448A=CA1882147352SETXc.4150T= (p.Ser1384=)
n.4334T=
9g.132327448A>CCA375327175SETXc.4150T>G (p.Ser1384Ala)
n.4334T>G
9g.132327448A>GCA375327177SETXc.4150T>C (p.Ser1384Pro)
n.4334T>C
9g.132327448A>TCA5297262SETXc.4150T>A (p.Ser1384Thr)
n.4334T>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.132327449A>CCA375327179SETXc.4149T>G (p.Asn1383Lys)
n.4333T>G
9g.132327449A>GCA467806937SETXc.4149T>C (p.Asn1383=)
n.4333T>C
9g.132327449A>TCA375327180SETXc.4149T>A (p.Asn1383Lys)
n.4333T>A
9g.132327450T>ACA375327185SETXc.4148A>T (p.Asn1383Ile)
n.4332A>T
9g.132327450T>CCA375327184SETXc.4148A>G (p.Asn1383Ser)
n.4332A>G
dbSNP
9g.132327450T>GCA375327183SETXc.4148A>C (p.Asn1383Thr)
n.4332A>C
9g.132327450T=CA1882147353SETXc.4148A= (p.Asn1383=)
n.4332A=
9g.132327451T>ACA375327186SETXc.4147A>T (p.Asn1383Tyr)
n.4331A>T
9g.132327451T>CCA375327188SETXc.4147A>G (p.Asn1383Asp)
n.4331A>G
9g.132327451T>GCA375327189SETXc.4147A>C (p.Asn1383His)
n.4331A>C
dbSNP gnomAD v2 gnomAD v4
9g.132327451T=CA1882147354SETXc.4147A= (p.Asn1383=)
n.4331A=
9g.132327452C>ACA375327191SETXc.4146G>T (p.Gln1382His)
n.4330G>T
gnomAD v4 COSMIC COSMIC
9g.132327452C=CA1882147355SETXc.4146G= (p.Gln1382=)
n.4330G=
9g.132327452C>GCA375327193SETXc.4146G>C (p.Gln1382His)
n.4330G>C
9g.132327452C>TCA5297263SETXc.4146G>A (p.Gln1382=)
n.4330G>A
dbSNP ExAC gnomAD v2 gnomAD v4
9g.132327453T>ACA375327198SETXc.4145A>T (p.Gln1382Leu)
n.4329A>T
9g.132327453T>CCA375327197SETXc.4145A>G (p.Gln1382Arg)
n.4329A>G
ClinVar
9g.132327453T>GCA375327195SETXc.4145A>C (p.Gln1382Pro)
n.4329A>C
9g.132327454G>ACA375327200SETXc.4144C>T (p.Gln1382Ter)
n.4328C>T
9g.132327454G>CCA375327201SETXc.4144C>G (p.Gln1382Glu)
n.4328C>G
gnomAD v4
9g.132327454G>TCA375327202SETXc.4144C>A (p.Gln1382Lys)
n.4328C>A
9g.132327455T>ACA467806952SETXc.4143A>T (p.Ala1381=)
n.4327A>T
9g.132327455T>CCA467806951SETXc.4143A>G (p.Ala1381=)
n.4327A>G
gnomAD v4
9g.132327455T>GCA200807327SETXc.4143A>C (p.Ala1381=)
n.4327A>C
dbSNP
9g.132327455T=CA1882147356SETXc.4143A= (p.Ala1381=)
n.4327A=
9g.132327456G>ACA200807334SETXc.4142C>T (p.Ala1381Val)
n.4326C>T
dbSNP
9g.132327456G>CCA375327203SETXc.4142C>G (p.Ala1381Gly)
n.4326C>G
9g.132327456G=CA1882147357SETXc.4142C= (p.Ala1381=)
n.4326C=
9g.132327456G>TCA375327204SETXc.4142C>A (p.Ala1381Glu)
n.4326C>A
9g.132327457C>ACA375327205SETXc.4141G>T (p.Ala1381Ser)
n.4325G>T
ClinVar
9g.132327457C>GCA375327207SETXc.4141G>C (p.Ala1381Pro)
n.4325G>C
9g.132327457C>TCA375327206SETXc.4141G>A (p.Ala1381Thr)
n.4325G>A
9g.132327458T>ACA467806959SETXc.4140A>T (p.Thr1380=)
n.4324A>T
9g.132327458T>CCA467806962SETXc.4140A>G (p.Thr1380=)
n.4324A>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.132327458T>GCA467806960SETXc.4140A>C (p.Thr1380=)
n.4324A>C
9g.132327458T=CA1882147358SETXc.4140A= (p.Thr1380=)
n.4324A=
9g.132327459G>ACA375327208SETXc.4139C>T (p.Thr1380Ile)
n.4323C>T
9g.132327459G>CCA375327209SETXc.4139C>G (p.Thr1380Arg)
n.4323C>G
9g.132327459G>TCA375327210SETXc.4139C>A (p.Thr1380Lys)
n.4323C>A
9g.132327460T>ACA375327211SETXc.4138A>T (p.Thr1380Ser)
n.4322A>T
9g.132327460T>CCA375327212SETXc.4138A>G (p.Thr1380Ala)
n.4322A>G
gnomAD v4
9g.132327460T>GCA375327213SETXc.4138A>C (p.Thr1380Pro)
n.4322A>C
gnomAD v4
9g.132327461A>CCA375327214SETXc.4137T>G (p.His1379Gln)
n.4321T>G
9g.132327461A>GCA467806969SETXc.4137T>C (p.His1379=)
n.4321T>C
gnomAD v4
9g.132327461A>TCA375327215SETXc.4137T>A (p.His1379Gln)
n.4321T>A
9g.132327462T>ACA375327216SETXc.4136A>T (p.His1379Leu)
n.4320A>T
9g.132327462T>CCA5297264SETXc.4136A>G (p.His1379Arg)
n.4320A>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.132327462T>GCA375327217SETXc.4136A>C (p.His1379Pro)
n.4320A>C
gnomAD v4
9g.132327462T=CA1882147359SETXc.4136A= (p.His1379=)
n.4320A=
9g.132327463G>ACA375327220SETXc.4135C>T (p.His1379Tyr)
n.4319C>T
gnomAD v4
9g.132327463G>CCA375327218SETXc.4135C>G (p.His1379Asp)
n.4319C>G
9g.132327463G>TCA375327219SETXc.4135C>A (p.His1379Asn)
n.4319C>A
9g.132327464T>ACA467806978SETXc.4134A>T (p.Ser1378=)
n.4318A>T
9g.132327464T>CCA467806980SETXc.4134A>G (p.Ser1378=)
n.4318A>G
gnomAD v4
9g.132327464T>GCA467806977SETXc.4134A>C (p.Ser1378=)
n.4318A>C
9g.132327465G>ACA375327221SETXc.4133C>T (p.Ser1378Leu)
n.4317C>T
dbSNP gnomAD v2 gnomAD v4
9g.132327465G>CCA375327222SETXc.4133C>G (p.Ser1378Ter)
n.4317C>G
9g.132327465G=CA1882147360SETXc.4133C= (p.Ser1378=)
n.4317C=
9g.132327465G>TCA375327223SETXc.4133C>A (p.Ser1378Ter)
n.4317C>A
9g.132327466A=CA1882147361SETXc.4132T= (p.Ser1378=)
n.4316T=
9g.132327466A>CCA5297265SETXc.4132T>G (p.Ser1378Ala)
n.4316T>G
dbSNP ExAC gnomAD v2 gnomAD v4
9g.132327466A>GCA375327224SETXc.4132T>C (p.Ser1378Pro)
n.4316T>C
9g.132327466A>TCA375327225SETXc.4132T>A (p.Ser1378Thr)
n.4316T>A
9g.132327467C>ACA467806990SETXc.4131G>T (p.Gly1377=)
n.4315G>T
9g.132327467C>GCA467806987SETXc.4131G>C (p.Gly1377=)
n.4315G>C
9g.132327467C>TCA467806988SETXc.4131G>A (p.Gly1377=)
n.4315G>A
9g.132327468C>ACA375327228SETXc.4130G>T (p.Gly1377Val)
n.4314G>T
9g.132327468C=CA1882147362SETXc.4130G= (p.Gly1377=)
n.4314G=
9g.132327468C>GCA375327227SETXc.4130G>C (p.Gly1377Ala)
n.4314G>C
dbSNP
9g.132327468C>TCA375327226SETXc.4130G>A (p.Gly1377Glu)
n.4314G>A
9g.132327469C>ACA375327229SETXc.4129G>T (p.Gly1377Trp)
n.4313G>T
9g.132327469C>GCA375327230SETXc.4129G>C (p.Gly1377Arg)
n.4313G>C
gnomAD v4
9g.132327469C>TCA375327231SETXc.4129G>A (p.Gly1377Arg)
n.4313G>A

Number of alleles fetched