Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.132327305T>ACA467807701SETXc.4293A>T (p.Pro1431=)
n.4477A>T
9g.132327305T>CCA467807702SETXc.4293A>G (p.Pro1431=)
n.4477A>G
9g.132327305T>GCA467807703SETXc.4293A>C (p.Pro1431=)
n.4477A>C
9g.132327306G>ACA375326641SETXc.4292C>T (p.Pro1431Leu)
n.4476C>T
dbSNP gnomAD v4
9g.132327306G>CCA375326642SETXc.4292C>G (p.Pro1431Arg)
n.4476C>G
9g.132327306G=CA1882147284SETXc.4292C= (p.Pro1431=)
n.4476C=
9g.132327306G>TCA375326643SETXc.4292C>A (p.Pro1431Gln)
n.4476C>A
9g.132327307G>ACA375326648SETXc.4291C>T (p.Pro1431Ser)
n.4475C>T
dbSNP gnomAD v2 gnomAD v4
9g.132327307G>CCA5297229SETXc.4291C>G (p.Pro1431Ala)
n.4475C>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.132327307G=CA1882147285SETXc.4291C= (p.Pro1431=)
n.4475C=
9g.132327307G>TCA375326646SETXc.4291C>A (p.Pro1431Thr)
n.4475C>A
9g.132327308A>CCA467807706SETXc.4290T>G (p.Ser1430=)
n.4474T>G
9g.132327308A>GCA467807705SETXc.4290T>C (p.Ser1430=)
n.4474T>C
9g.132327308A>TCA467807704SETXc.4290T>A (p.Ser1430=)
n.4474T>A
9g.132327309G>ACA375326649SETXc.4289C>T (p.Ser1430Phe)
n.4473C>T
9g.132327309G>CCA375326651SETXc.4289C>G (p.Ser1430Cys)
n.4473C>G
9g.132327309G>TCA375326653SETXc.4289C>A (p.Ser1430Tyr)
n.4473C>A
gnomAD v4
9g.132327310A>CCA375326655SETXc.4288T>G (p.Ser1430Ala)
n.4472T>G
9g.132327310A>GCA375326656SETXc.4288T>C (p.Ser1430Pro)
n.4472T>C
9g.132327310A>TCA375326658SETXc.4288T>A (p.Ser1430Thr)
n.4472T>A
9g.132327311C>ACA467807707SETXc.4287G>T (p.Gly1429=)
n.4471G>T
9g.132327311C=CA1882147286SETXc.4287G= (p.Gly1429=)
n.4471G=
9g.132327311C>GCA467807708SETXc.4287G>C (p.Gly1429=)
n.4471G>C
9g.132327311C>TCA200807146SETXc.4287G>A (p.Gly1429=)
n.4471G>A
dbSNP gnomAD v3 gnomAD v4
9g.132327312C>ACA375326661SETXc.4286G>T (p.Gly1429Val)
n.4470G>T
9g.132327312C>GCA375326663SETXc.4286G>C (p.Gly1429Ala)
n.4470G>C
9g.132327312C>TCA375326662SETXc.4286G>A (p.Gly1429Glu)
n.4470G>A
9g.132327313C>ACA375326665SETXc.4285G>T (p.Gly1429Trp)
n.4469G>T
9g.132327313C>GCA375326667SETXc.4285G>C (p.Gly1429Arg)
n.4469G>C
9g.132327313C>TCA375326668SETXc.4285G>A (p.Gly1429Arg)
n.4469G>A
9g.132327314A=CA1882147287SETXc.4284T= (p.His1428=)
n.4468T=
9g.132327314A>CCA375326669SETXc.4284T>G (p.His1428Gln)
n.4468T>G
9g.132327314A>GCA467807709SETXc.4284T>C (p.His1428=)
n.4468T>C
dbSNP
9g.132327314A>TCA375326671SETXc.4284T>A (p.His1428Gln)
n.4468T>A
9g.132327315T>ACA375326673SETXc.4283A>T (p.His1428Leu)
n.4467A>T
9g.132327315T>CCA5297230SETXc.4283A>G (p.His1428Arg)
n.4467A>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.132327315T>GCA375326675SETXc.4283A>C (p.His1428Pro)
n.4467A>C
9g.132327315T=CA1882147288SETXc.4283A= (p.His1428=)
n.4467A=
9g.132327316G>ACA375326677SETXc.4282C>T (p.His1428Tyr)
n.4466C>T
9g.132327316G>CCA375326678SETXc.4282C>G (p.His1428Asp)
n.4466C>G
9g.132327316G>TCA375326680SETXc.4282C>A (p.His1428Asn)
n.4466C>A
9g.132327317T>ACA375326683SETXc.4281A>T (p.Lys1427Asn)
n.4465A>T
9g.132327317T>CCA467807710SETXc.4281A>G (p.Lys1427=)
n.4465A>G
9g.132327317T>GCA375326681SETXc.4281A>C (p.Lys1427Asn)
n.4465A>C
9g.132327318T>ACA375326684SETXc.4280A>T (p.Lys1427Ile)
n.4464A>T
9g.132327318T>CCA375326686SETXc.4280A>G (p.Lys1427Arg)
n.4464A>G
9g.132327318T>GCA375326685SETXc.4280A>C (p.Lys1427Thr)
n.4464A>C
9g.132327319T>ACA375326687SETXc.4279A>T (p.Lys1427Ter)
n.4463A>T
9g.132327319T>CCA375326689SETXc.4279A>G (p.Lys1427Glu)
n.4463A>G
9g.132327319T>GCA375326690SETXc.4279A>C (p.Lys1427Gln)
n.4463A>C
9g.132327320T>ACA467807713SETXc.4278A>T (p.Ala1426=)
n.4462A>T
9g.132327320T>CCA467807712SETXc.4278A>G (p.Ala1426=)
n.4462A>G
9g.132327320T>GCA467807711SETXc.4278A>C (p.Ala1426=)
n.4462A>C
9g.132327321G>ACA375326692SETXc.4277C>T (p.Ala1426Val)
n.4461C>T
dbSNP
9g.132327321G>CCA375326694SETXc.4277C>G (p.Ala1426Gly)
n.4461C>G
9g.132327321G>TCA375326696SETXc.4277C>A (p.Ala1426Glu)
n.4461C>A
9g.132327322C>ACA375326697SETXc.4276G>T (p.Ala1426Ser)
n.4460G>T
dbSNP
9g.132327322C>GCA375326698SETXc.4276G>C (p.Ala1426Pro)
n.4460G>C
9g.132327322C>TCA375326700SETXc.4276G>A (p.Ala1426Thr)
n.4460G>A
gnomAD v4
9g.132327323T>ACA375326702SETXc.4275A>T (p.Lys1425Asn)
n.4459A>T
gnomAD v4
9g.132327323T>CCA467807714SETXc.4275A>G (p.Lys1425=)
n.4459A>G
dbSNP
9g.132327323T>GCA375326703SETXc.4275A>C (p.Lys1425Asn)
n.4459A>C
9g.132327323T=CA1882147289SETXc.4275A= (p.Lys1425=)
n.4459A=
9g.132327324_132327328delCA2692256380SETXc.4271_4275del (p.Ile1424SerfsTer9)
n.4455_4459del
gnomAD v4
9g.132327324T>ACA375326708SETXc.4274A>T (p.Lys1425Ile)
n.4458A>T
9g.132327324T>CCA375326706SETXc.4274A>G (p.Lys1425Arg)
n.4458A>G
9g.132327324T>GCA375326705SETXc.4274A>C (p.Lys1425Thr)
n.4458A>C
9g.132327325T>ACA375326710SETXc.4273A>T (p.Lys1425Ter)
n.4457A>T
9g.132327325T>CCA233102SETXc.4273A>G (p.Lys1425Glu)
n.4457A>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.132327325T>GCA375326712SETXc.4273A>C (p.Lys1425Gln)
n.4457A>C
9g.132327325T=CA1882147290SETXc.4273A= (p.Lys1425=)
n.4457A=
9g.132327326T>ACA467807715SETXc.4272A>T (p.Ile1424=)
n.4456A>T
9g.132327326T>CCA375326714SETXc.4272A>G (p.Ile1424Met)
n.4456A>G
9g.132327326T>GCA467807716SETXc.4272A>C (p.Ile1424=)
n.4456A>C
gnomAD v4
9g.132327327A>CCA375326715SETXc.4271T>G (p.Ile1424Arg)
n.4455T>G
9g.132327327A>GCA375326716SETXc.4271T>C (p.Ile1424Thr)
n.4455T>C
gnomAD v4
9g.132327327A>TCA375326718SETXc.4271T>A (p.Ile1424Lys)
n.4455T>A
9g.132327328T>ACA375326719SETXc.4270A>T (p.Ile1424Leu)
n.4454A>T
9g.132327328T>CCA5297231SETXc.4270A>G (p.Ile1424Val)
n.4454A>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.132327328T>GCA375326721SETXc.4270A>C (p.Ile1424Leu)
n.4454A>C
9g.132327328T=CA1882147291SETXc.4270A= (p.Ile1424=)
n.4454A=
9g.132327329G>ACA467807717SETXc.4269C>T (p.Thr1423=)
n.4453C>T
9g.132327329G>CCA467807718SETXc.4269C>G (p.Thr1423=)
n.4453C>G
9g.132327329G>TCA467807719SETXc.4269C>A (p.Thr1423=)
n.4453C>A
9g.132327330G>ACA375326722SETXc.4268C>T (p.Thr1423Ile)
n.4452C>T
dbSNP gnomAD v3 gnomAD v4
9g.132327330G>CCA375326724SETXc.4268C>G (p.Thr1423Ser)
n.4452C>G
9g.132327330G=CA1882147292SETXc.4268C= (p.Thr1423=)
n.4452C=
9g.132327330G>TCA375326725SETXc.4268C>A (p.Thr1423Asn)
n.4452C>A
9g.132327331T>ACA375326731SETXc.4267A>T (p.Thr1423Ser)
n.4451A>T
9g.132327331T>CCA375326729SETXc.4267A>G (p.Thr1423Ala)
n.4451A>G
dbSNP gnomAD v4
9g.132327331T>GCA375326727SETXc.4267A>C (p.Thr1423Pro)
n.4451A>C
9g.132327331T=CA1882147293SETXc.4267A= (p.Thr1423=)
n.4451A=
9g.132327332T>ACA375326734SETXc.4266A>T (p.Glu1422Asp)
n.4450A>T
9g.132327332T>CCA467807720SETXc.4266A>G (p.Glu1422=)
n.4450A>G
9g.132327332T>GCA375326732SETXc.4266A>C (p.Glu1422Asp)
n.4450A>C
9g.132327333T>ACA375326738SETXc.4265A>T (p.Glu1422Val)
n.4449A>T
9g.132327333T>CCA375326736SETXc.4265A>G (p.Glu1422Gly)
n.4449A>G
9g.132327333T>GCA375326739SETXc.4265A>C (p.Glu1422Ala)
n.4449A>C
gnomAD v4
9g.132327334C>ACA375326741SETXc.4264G>T (p.Glu1422Ter)
n.4448G>T
9g.132327334C>GCA375326742SETXc.4264G>C (p.Glu1422Gln)
n.4448G>C
9g.132327334C>TCA375326744SETXc.4264G>A (p.Glu1422Lys)
n.4448G>A
9g.132327335T>ACA467807721SETXc.4263A>T (p.Pro1421=)
n.4447A>T
9g.132327335T>CCA467807722SETXc.4263A>G (p.Pro1421=)
n.4447A>G
9g.132327335T>GCA5297232SETXc.4263A>C (p.Pro1421=)
n.4447A>C
dbSNP ExAC gnomAD v2
9g.132327335T=CA1882147294SETXc.4263A= (p.Pro1421=)
n.4447A=
9g.132327336G>ACA375326747SETXc.4262C>T (p.Pro1421Leu)
n.4446C>T
9g.132327336G>CCA200807172SETXc.4262C>G (p.Pro1421Arg)
n.4446C>G
ClinVar dbSNP gnomAD v3 gnomAD v4
9g.132327336G=CA1882147295SETXc.4262C= (p.Pro1421=)
n.4446C=
9g.132327336G>TCA375326750SETXc.4262C>A (p.Pro1421Gln)
n.4446C>A
9g.132327337G>ACA375326752SETXc.4261C>T (p.Pro1421Ser)
n.4445C>T
gnomAD v4
9g.132327337G>CCA375326759SETXc.4261C>G (p.Pro1421Ala)
n.4445C>G
dbSNP gnomAD v4
9g.132327337G>TCA375326761SETXc.4261C>A (p.Pro1421Thr)
n.4445C>A
9g.132327338T>ACA375326765SETXc.4260A>T (p.Glu1420Asp)
n.4444A>T
gnomAD v4
9g.132327338T>CCA467807723SETXc.4260A>G (p.Glu1420=)
n.4444A>G
gnomAD v4
9g.132327338T>GCA375326767SETXc.4260A>C (p.Glu1420Asp)
n.4444A>C
9g.132327339T>ACA375326773SETXc.4259A>T (p.Glu1420Val)
n.4443A>T
9g.132327339T>CCA375326768SETXc.4259A>G (p.Glu1420Gly)
n.4443A>G
ClinVar
9g.132327339T>GCA375326770SETXc.4259A>C (p.Glu1420Ala)
n.4443A>C
dbSNP gnomAD v3 gnomAD v4
9g.132327339T=CA1882147296SETXc.4259A= (p.Glu1420=)
n.4443A=
9g.132327340C>ACA375326775SETXc.4258G>T (p.Glu1420Ter)
n.4442G>T
9g.132327340C>GCA375326777SETXc.4258G>C (p.Glu1420Gln)
n.4442G>C
9g.132327340C>TCA375326778SETXc.4258G>A (p.Glu1420Lys)
n.4442G>A
9g.132327341A>CCA467807724SETXc.4257T>G (p.Ser1419=)
n.4441T>G
9g.132327341A>GCA467807725SETXc.4257T>C (p.Ser1419=)
n.4441T>C
9g.132327341A>TCA467807726SETXc.4257T>A (p.Ser1419=)
n.4441T>A
9g.132327342G>ACA375326780SETXc.4256C>T (p.Ser1419Phe)
n.4440C>T
gnomAD v4
9g.132327342G>CCA375326782SETXc.4256C>G (p.Ser1419Cys)
n.4440C>G
9g.132327342G>TCA375326784SETXc.4256C>A (p.Ser1419Tyr)
n.4440C>A
9g.132327343A>CCA375326785SETXc.4255T>G (p.Ser1419Ala)
n.4439T>G
9g.132327343A>GCA375326787SETXc.4255T>C (p.Ser1419Pro)
n.4439T>C
9g.132327343A>TCA375326788SETXc.4255T>A (p.Ser1419Thr)
n.4439T>A
9g.132327344A>CCA467807727SETXc.4254T>G (p.Pro1418=)
n.4438T>G
9g.132327344A>GCA467807728SETXc.4254T>C (p.Pro1418=)
n.4438T>C
9g.132327344A>TCA467807729SETXc.4254T>A (p.Pro1418=)
n.4438T>A
9g.132327345G>ACA375326790SETXc.4253C>T (p.Pro1418Leu)
n.4437C>T
dbSNP gnomAD v4
9g.132327345G>CCA375326793SETXc.4253C>G (p.Pro1418Arg)
n.4437C>G
dbSNP gnomAD v2 gnomAD v4
9g.132327345G=CA1882147297SETXc.4253C= (p.Pro1418=)
n.4437C=
9g.132327345G>TCA375326795SETXc.4253C>A (p.Pro1418His)
n.4437C>A
dbSNP
9g.132327346G>ACA375326798SETXc.4252C>T (p.Pro1418Ser)
n.4436C>T
9g.132327346G>CCA5297233SETXc.4252C>G (p.Pro1418Ala)
n.4436C>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.132327346G=CA1882147298SETXc.4252C= (p.Pro1418=)
n.4436C=
9g.132327346G>TCA375326797SETXc.4252C>A (p.Pro1418Thr)
n.4436C>A
9g.132327347C>ACA375326803SETXc.4251G>T (p.Met1417Ile)
n.4435G>T
9g.132327347C=CA1882147299SETXc.4251G= (p.Met1417=)
n.4435G=
9g.132327347C>GCA375326799SETXc.4251G>C (p.Met1417Ile)
n.4435G>C
dbSNP
9g.132327347C>TCA375326801SETXc.4251G>A (p.Met1417Ile)
n.4435G>A
9g.132327348A>CCA375326804SETXc.4250T>G (p.Met1417Arg)
n.4434T>G
9g.132327348A>GCA375326805SETXc.4250T>C (p.Met1417Thr)
n.4434T>C
9g.132327348A>TCA375326809SETXc.4250T>A (p.Met1417Lys)
n.4434T>A
9g.132327349T>ACA375326814SETXc.4249A>T (p.Met1417Leu)
n.4433A>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.132327349T>CCA375326813SETXc.4249A>G (p.Met1417Val)
n.4433A>G
dbSNP
9g.132327349T>GCA375326811SETXc.4249A>C (p.Met1417Leu)
n.4433A>C
9g.132327349T=CA1882147300SETXc.4249A= (p.Met1417=)
n.4433A=
9g.132327350G>ACA5297235SETXc.4248C>T (p.Cys1416=)
n.4432C>T
dbSNP ExAC gnomAD v2 gnomAD v4
9g.132327350G>CCA5297234SETXc.4248C>G (p.Cys1416Trp)
n.4432C>G
dbSNP ExAC gnomAD v2
9g.132327350G=CA1882147301SETXc.4248C= (p.Cys1416=)
n.4432C=
9g.132327350G>TCA375326817SETXc.4248C>A (p.Cys1416Ter)
n.4432C>A
9g.132327351C>ACA375326818SETXc.4247G>T (p.Cys1416Phe)
n.4431G>T
9g.132327351C>GCA375326819SETXc.4247G>C (p.Cys1416Ser)
n.4431G>C
9g.132327351C>TCA375326820SETXc.4247G>A (p.Cys1416Tyr)
n.4431G>A
COSMIC COSMIC
9g.132327352A=CA1882147302SETXc.4246T= (p.Cys1416=)
n.4430T=
9g.132327352A>CCA375326822SETXc.4246T>G (p.Cys1416Gly)
n.4430T>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.132327352A>GCA375326825SETXc.4246T>C (p.Cys1416Arg)
n.4430T>C
9g.132327352A>TCA5297236SETXc.4246T>A (p.Cys1416Ser)
n.4430T>A
dbSNP ExAC gnomAD v2 gnomAD v4
9g.132327353T>ACA375326827SETXc.4245A>T (p.Lys1415Asn)
n.4429A>T
9g.132327353T>CCA467807730SETXc.4245A>G (p.Lys1415=)
n.4429A>G
9g.132327353T>GCA375326828SETXc.4245A>C (p.Lys1415Asn)
n.4429A>C
9g.132327354T>ACA375326830SETXc.4244A>T (p.Lys1415Ile)
n.4428A>T
9g.132327354T>CCA375326831SETXc.4244A>G (p.Lys1415Arg)
n.4428A>G
gnomAD v4
9g.132327354T>GCA375326834SETXc.4244A>C (p.Lys1415Thr)
n.4428A>C
9g.132327355T>ACA375326840SETXc.4243A>T (p.Lys1415Ter)
n.4427A>T
9g.132327355T>CCA375326843SETXc.4243A>G (p.Lys1415Glu)
n.4427A>G
9g.132327355T>GCA375326845SETXc.4243A>C (p.Lys1415Gln)
n.4427A>C
9g.132327356T>ACA467807731SETXc.4242A>T (p.Ile1414=)
n.4426A>T
9g.132327356T>CCA375326846SETXc.4242A>G (p.Ile1414Met)
n.4426A>G
gnomAD v4
9g.132327356T>GCA467807732SETXc.4242A>C (p.Ile1414=)
n.4426A>C
9g.132327357A>CCA375326847SETXc.4241T>G (p.Ile1414Arg)
n.4425T>G
9g.132327357A>GCA375326848SETXc.4241T>C (p.Ile1414Thr)
n.4425T>C
9g.132327357A>TCA375326849SETXc.4241T>A (p.Ile1414Lys)
n.4425T>A
9g.132327358T>ACA375326853SETXc.4240A>T (p.Ile1414Leu)
n.4424A>T
9g.132327358T>CCA5297237SETXc.4240A>G (p.Ile1414Val)
n.4424A>G
dbSNP ExAC gnomAD v2 gnomAD v4
9g.132327358T>GCA375326851SETXc.4240A>C (p.Ile1414Leu)
n.4424A>C
9g.132327358T=CA1882147303SETXc.4240A= (p.Ile1414=)
n.4424A=
9g.132327359T>ACA375326855SETXc.4239A>T (p.Leu1413Phe)
n.4423A>T
9g.132327359T>CCA467807733SETXc.4239A>G (p.Leu1413=)
n.4423A>G
9g.132327359T>GCA375326856SETXc.4239A>C (p.Leu1413Phe)
n.4423A>C
9g.132327359_132327364delinsTAACTGCA1882147304SETXc.4234_4239delinsCAGTTA (p.Gln1412=)
n.4418_4423delinsCAGTTA
9g.132327360A=CA1882147305SETXc.4238T= (p.Leu1413=)
n.4422T=
9g.132327360A>CCA375326859SETXc.4238T>G (p.Leu1413Ter)
n.4422T>G
9g.132327360A>GCA375326860SETXc.4238T>C (p.Leu1413Ser)
n.4422T>C
dbSNP gnomAD v2 gnomAD v4
9g.132327360A>TCA375326862SETXc.4238T>A (p.Leu1413Ter)
n.4422T>A
dbSNP gnomAD v2 gnomAD v4
9g.132327360_132327364delCA1129644153SETXc.4234_4238del (p.Gln1412AsnfsTer7)
n.4418_4422del
dbSNP gnomAD v3 gnomAD v4
9g.132327361A>CCA375326864SETXc.4237T>G (p.Leu1413Val)
n.4421T>G
9g.132327361A>GCA467807734SETXc.4237T>C (p.Leu1413=)
n.4421T>C
9g.132327361A>TCA375326866SETXc.4237T>A (p.Leu1413Ile)
n.4421T>A
9g.132327362C>ACA375326867SETXc.4236G>T (p.Gln1412His)
n.4420G>T
9g.132327362C>GCA375326869SETXc.4236G>C (p.Gln1412His)
n.4420G>C
9g.132327362C>TCA467807735SETXc.4236G>A (p.Gln1412=)
n.4420G>A
9g.132327363T>ACA5297238SETXc.4235A>T (p.Gln1412Leu)
n.4419A>T
dbSNP ExAC gnomAD v2 gnomAD v4
9g.132327363T>CCA375326871SETXc.4235A>G (p.Gln1412Arg)
n.4419A>G
dbSNP gnomAD v2 gnomAD v4
9g.132327363T>GCA375326873SETXc.4235A>C (p.Gln1412Pro)
n.4419A>C
9g.132327363T=CA1882147306SETXc.4235A= (p.Gln1412=)
n.4419A=
9g.132327364G>ACA375326876SETXc.4234C>T (p.Gln1412Ter)
n.4418C>T
9g.132327364G>CCA375326878SETXc.4234C>G (p.Gln1412Glu)
n.4418C>G
dbSNP gnomAD v2 gnomAD v4
9g.132327364G=CA1882147307SETXc.4234C= (p.Gln1412=)
n.4418C=
9g.132327364G>TCA375326880SETXc.4234C>A (p.Gln1412Lys)
n.4418C>A
9g.132327365T>ACA375326882SETXc.4233A>T (p.Lys1411Asn)
n.4417A>T
9g.132327365T>CCA5297239SETXc.4233A>G (p.Lys1411=)
n.4417A>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.132327365T>GCA375326883SETXc.4233A>C (p.Lys1411Asn)
n.4417A>C
9g.132327365T=CA1882147308SETXc.4233A= (p.Lys1411=)
n.4417A=
9g.132327368delCA2579491636SETXc.4233del (p.Lys1411AsnfsTer3)
n.4417del
9g.132327366T>ACA375326886SETXc.4232A>T (p.Lys1411Ile)
n.4416A>T
9g.132327366T>CCA375326887SETXc.4232A>G (p.Lys1411Arg)
n.4416A>G
9g.132327366T>GCA375326889SETXc.4232A>C (p.Lys1411Thr)
n.4416A>C
9g.132327367T>ACA375326891SETXc.4231A>T (p.Lys1411Ter)
n.4415A>T
9g.132327367T>CCA5297240SETXc.4231A>G (p.Lys1411Glu)
n.4415A>G
dbSNP ExAC gnomAD v2 gnomAD v4
9g.132327367T>GCA375326893SETXc.4231A>C (p.Lys1411Gln)
n.4415A>C
9g.132327367T=CA1882147309SETXc.4231A= (p.Lys1411=)
n.4415A=
9g.132327368T>ACA375326895SETXc.4230A>T (p.Arg1410Ser)
n.4414A>T
9g.132327368T>CCA467807736SETXc.4230A>G (p.Arg1410=)
n.4414A>G
9g.132327368T>GCA5297241SETXc.4230A>C (p.Arg1410Ser)
n.4414A>C
dbSNP ExAC gnomAD v2 gnomAD v4
9g.132327368T=CA1882147310SETXc.4230A= (p.Arg1410=)
n.4414A=
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

Number of alleles fetched