Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.49457976A=CA1627395391MMUTc.468T= (p.Asp156=)
6g.49457976A>CCA364404667MMUTc.468T>G (p.Asp156Glu)
6g.49457976A>GCA450608655MMUTc.468T>C (p.Asp156=)
gnomAD v4
6g.49457976A>TCA364404668MMUTc.468T>A (p.Asp156Glu)
dbSNP
6g.49457977T>ACA3847103MMUTc.467A>T (p.Asp156Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
6g.49457977T>CCA364404669MMUTc.467A>G (p.Asp156Gly)
dbSNP gnomAD v3 gnomAD v4
6g.49457977T>GCA364404670MMUTc.467A>C (p.Asp156Ala)
6g.49457977T=CA1627395396MMUTc.467A= (p.Asp156=)
6g.49457978C>ACA364404671MMUTc.466G>T (p.Asp156Tyr)
6g.49457978C>GCA364404672MMUTc.466G>C (p.Asp156His)
6g.49457978C>TCA364404673MMUTc.466G>A (p.Asp156Asn)
ClinVar gnomAD v4
6g.49457981_49457983delCA2695206689MMUTc.464_466del (p.Gly155del)
6g.49457979A>CCA450608658MMUTc.465T>G (p.Gly155=)
6g.49457979A>GCA450608659MMUTc.465T>C (p.Gly155=)
6g.49457979A>TCA450608660MMUTc.465T>A (p.Gly155=)
6g.49457980C>ACA364404674MMUTc.464G>T (p.Gly155Val)
gnomAD v4
6g.49457980C=CA1627395403MMUTc.464G= (p.Gly155=)
6g.49457980C>GCA364404675MMUTc.464G>C (p.Gly155Ala)
6g.49457980C>TCA3847104MMUTc.464G>A (p.Gly155Asp)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49457981C>ACA364404677MMUTc.463G>T (p.Gly155Cys)
gnomAD v4
6g.49457981C>GCA364404678MMUTc.463G>C (p.Gly155Arg)
6g.49457981C>TCA364404676MMUTc.463G>A (p.Gly155Ser)
6g.49457982A>CCA450608661MMUTc.462T>G (p.Arg154=)
6g.49457982A>GCA450608662MMUTc.462T>C (p.Arg154=)
6g.49457982A>TCA450608663MMUTc.462T>A (p.Arg154=)
gnomAD v4
6g.49457983C>ACA364404680MMUTc.461G>T (p.Arg154Leu)
gnomAD v4
6g.49457983C=CA1627395411MMUTc.461G= (p.Arg154=)
6g.49457983C>GCA364404679MMUTc.461G>C (p.Arg154Pro)
6g.49457983C>TCA3847105MMUTc.461G>A (p.Arg154His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49457984G>ACA364404681MMUTc.460C>T (p.Arg154Cys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.49457984G>CCA364404682MMUTc.460C>G (p.Arg154Gly)
6g.49457984G=CA1627395419MMUTc.460C= (p.Arg154=)
6g.49457984G>TCA364404683MMUTc.460C>A (p.Arg154Ser)
gnomAD v4
6g.49457985A>CCA450608665MMUTc.459T>G (p.Val153=)
6g.49457985A>GCA450608666MMUTc.459T>C (p.Val153=)
6g.49457985A>TCA450608667MMUTc.459T>A (p.Val153=)
6g.49457986delCA2695206690MMUTc.459del (p.Arg154ValfsTer26)
6g.49457986A>CCA364404684MMUTc.458T>G (p.Val153Gly)
6g.49457986A>GCA364404685MMUTc.458T>C (p.Val153Ala)
6g.49457986A>TCA364404686MMUTc.458T>A (p.Val153Asp)
6g.49457987C>ACA364404687MMUTc.457G>T (p.Val153Phe)
6g.49457987C=CA1627395424MMUTc.457G= (p.Val153=)
6g.49457987C>GCA364404688MMUTc.457G>C (p.Val153Leu)
6g.49457987C>TCA364404689MMUTc.457G>A (p.Val153Ile)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.49457988T>ACA450608670MMUTc.456A>T (p.Arg152=)
6g.49457988T>CCA450608669MMUTc.456A>G (p.Arg152=)
6g.49457988T>GCA450608668MMUTc.456A>C (p.Arg152=)
6g.49457989C>ACA364404691MMUTc.455G>T (p.Arg152Leu)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.49457989C=CA1627395431MMUTc.455G= (p.Arg152=)
6g.49457989C>GCA364404690MMUTc.455G>C (p.Arg152Pro)
6g.49457989C>TCA3847106MMUTc.455G>A (p.Arg152Gln)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.49457990G>ACA3847107MMUTc.454C>T (p.Arg152Ter)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49457990G>CCA364404692MMUTc.454C>G (p.Arg152Gly)
6g.49457990G=CA1627395439MMUTc.454C= (p.Arg152=)
6g.49457990G>TCA450608671MMUTc.454C>A (p.Arg152=)
6g.49457991A>CCA450608672MMUTc.453T>G (p.Pro151=)
6g.49457991A>GCA450608673MMUTc.453T>C (p.Pro151=)
6g.49457991A>TCA450608674MMUTc.453T>A (p.Pro151=)
6g.49457992G>ACA364404693MMUTc.452C>T (p.Pro151Leu)
ClinVar dbSNP gnomAD v3 gnomAD v4
6g.49457992G>CCA364404694MMUTc.452C>G (p.Pro151Arg)
gnomAD v4
6g.49457992G=CA1627395441MMUTc.452C= (p.Pro151=)
6g.49457992G>TCA364404695MMUTc.452C>A (p.Pro151His)
6g.49457993G>ACA364404696MMUTc.451C>T (p.Pro151Ser)
gnomAD v4 COSMIC
6g.49457993G>CCA364404697MMUTc.451C>G (p.Pro151Ala)
6g.49457993G>TCA364404698MMUTc.451C>A (p.Pro151Thr)
6g.49457994G>ACA450608675MMUTc.450C>T (p.Asn150=)
ClinVar dbSNP gnomAD v4
6g.49457994G>CCA364404699MMUTc.450C>G (p.Asn150Lys)
6g.49457994G=CA1627395443MMUTc.450C= (p.Asn150=)
6g.49457994G>TCA364404700MMUTc.450C>A (p.Asn150Lys)
6g.49457995T>ACA364404701MMUTc.449A>T (p.Asn150Ile)
6g.49457995T>CCA138799965MMUTc.449A>G (p.Asn150Ser)
dbSNP gnomAD v3 gnomAD v4
6g.49457995T>GCA364404702MMUTc.449A>C (p.Asn150Thr)
6g.49457995T=CA1627395447MMUTc.449A= (p.Asn150=)
6g.49457996T>ACA364404704MMUTc.448A>T (p.Asn150Tyr)
6g.49457996T>CCA364404705MMUTc.448A>G (p.Asn150Asp)
6g.49457996T>GCA364404703MMUTc.448A>C (p.Asn150His)
6g.49457997G>ACA450608676MMUTc.447C>T (p.Asp149=)
gnomAD v4
6g.49457997G>CCA364404706MMUTc.447C>G (p.Asp149Glu)
6g.49457997G=CA1627395449MMUTc.447C= (p.Asp149=)
6g.49457997G>TCA364404707MMUTc.447C>A (p.Asp149Glu)
ClinVar
6g.49457998T>ACA364404708MMUTc.446A>T (p.Asp149Val)
ClinVar dbSNP
6g.49457998T>CCA364404709MMUTc.446A>G (p.Asp149Gly)
ClinVar dbSNP gnomAD v3 gnomAD v4
6g.49457998T>GCA364404710MMUTc.446A>C (p.Asp149Ala)
6g.49457998T=CA1627395460MMUTc.446A= (p.Asp149=)
6g.49457998dupCA1139659603MMUTc.446dup (p.Asp149GlufsTer8)
ClinVar dbSNP
6g.49457999C>ACA364404711MMUTc.445G>T (p.Asp149Tyr)
6g.49457999C>GCA364404712MMUTc.445G>C (p.Asp149His)
6g.49457999C>TCA364404713MMUTc.445G>A (p.Asp149Asn)
6g.49458000T>ACA450608677MMUTc.444A>T (p.Ser148=)
6g.49458000T>CCA450608678MMUTc.444A>G (p.Ser148=)
6g.49458000T>GCA450608679MMUTc.444A>C (p.Ser148=)
dbSNP gnomAD v2 gnomAD v4
6g.49458000T=CA1627395465MMUTc.444A= (p.Ser148=)
6g.49458001G>ACA364404714MMUTc.443C>T (p.Ser148Leu)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.49458001G>CCA364404715MMUTc.443C>G (p.Ser148Ter)
dbSNP gnomAD v2 gnomAD v4
6g.49458001G=CA1627395469MMUTc.443C= (p.Ser148=)
6g.49458001G>TCA364404716MMUTc.443C>A (p.Ser148Ter)
6g.49458002A>CCA364404717MMUTc.442T>G (p.Ser148Ala)
6g.49458002A>GCA364404718MMUTc.442T>C (p.Ser148Pro)
6g.49458002A>TCA364404719MMUTc.442T>A (p.Ser148Thr)
6g.49458003A>CCA364404721MMUTc.441T>G (p.Asp147Glu)
6g.49458003A>GCA450608680MMUTc.441T>C (p.Asp147=)
gnomAD v4
6g.49458003A>TCA364404720MMUTc.441T>A (p.Asp147Glu)
6g.49458004T>ACA364404722MMUTc.440A>T (p.Asp147Val)
6g.49458004T>CCA364404723MMUTc.440A>G (p.Asp147Gly)
6g.49458004T>GCA364404724MMUTc.440A>C (p.Asp147Ala)
6g.49458005C>ACA364404725MMUTc.439G>T (p.Asp147Tyr)
gnomAD v4
6g.49458005C>GCA364404726MMUTc.439G>C (p.Asp147His)
6g.49458005C>TCA364404727MMUTc.439G>A (p.Asp147Asn)
6g.49458006delCA2582341703MMUTc.438del (p.Tyr146Ter)
ClinVar
6g.49458006A=CA1627395472MMUTc.438T= (p.Tyr146=)
6g.49458006A>CCA364404729MMUTc.438T>G (p.Tyr146Ter)
6g.49458006A>GCA3847108MMUTc.438T>C (p.Tyr146=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49458006A>TCA364404728MMUTc.438T>A (p.Tyr146Ter)
ClinVar dbSNP
6g.49458007T>ACA364404730MMUTc.437A>T (p.Tyr146Phe)
6g.49458007T>CCA3847109MMUTc.437A>G (p.Tyr146Cys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49458007T>GCA364404731MMUTc.437A>C (p.Tyr146Ser)
6g.49458007T=CA1627395476MMUTc.437A= (p.Tyr146=)
6g.49458008A>CCA364404732MMUTc.436T>G (p.Tyr146Asp)
6g.49458008A>GCA364404733MMUTc.436T>C (p.Tyr146His)
6g.49458008A>TCA364404734MMUTc.436T>A (p.Tyr146Asn)
6g.49458008dupCA2695206691MMUTc.436dup (p.Tyr146LeufsTer2)
6g.49458009G>ACA450608681MMUTc.435C>T (p.Gly145=)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
6g.49458009G>CCA450608682MMUTc.435C>G (p.Gly145=)
6g.49458009G=CA1627395481MMUTc.435C= (p.Gly145=)
6g.49458009G>TCA450608683MMUTc.435C>A (p.Gly145=)
6g.49458010C>ACA364404736MMUTc.434G>T (p.Gly145Val)
dbSNP gnomAD v2 gnomAD v4
6g.49458010C=CA1627395482MMUTc.434G= (p.Gly145=)
6g.49458010C>GCA364404737MMUTc.434G>C (p.Gly145Ala)
6g.49458010C>TCA364404735MMUTc.434G>A (p.Gly145Asp)
gnomAD v4 COSMIC
6g.49458011C>ACA364404738MMUTc.433G>T (p.Gly145Cys)
dbSNP gnomAD v2
6g.49458011C=CA1627395484MMUTc.433G= (p.Gly145=)
6g.49458011C>GCA364404740MMUTc.433G>C (p.Gly145Arg)
6g.49458011C>TCA364404739MMUTc.433G>A (p.Gly145Ser)
dbSNP gnomAD v4
6g.49458012A>CCA450608684MMUTc.432T>G (p.Arg144=)
6g.49458012A>GCA450608685MMUTc.432T>C (p.Arg144=)
6g.49458012A>TCA450608686MMUTc.432T>A (p.Arg144=)
6g.49458013C>ACA364404741MMUTc.431G>T (p.Arg144Leu)
6g.49458013C=CA1627395489MMUTc.431G= (p.Arg144=)
6g.49458013C>GCA364404742MMUTc.431G>C (p.Arg144Pro)
6g.49458013C>TCA3847110MMUTc.431G>A (p.Arg144His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49458014G>ACA364404743MMUTc.430C>T (p.Arg144Cys)
ClinVar gnomAD v4
6g.49458014G>CCA364404745MMUTc.430C>G (p.Arg144Gly)
gnomAD v4
6g.49458014G>TCA364404744MMUTc.430C>A (p.Arg144Ser)
6g.49458015A>CCA364404746MMUTc.429T>G (p.His143Gln)
6g.49458015A>GCA450608687MMUTc.429T>C (p.His143=)
6g.49458015A>TCA364404747MMUTc.429T>A (p.His143Gln)
6g.49458016T>ACA364404748MMUTc.428A>T (p.His143Leu)
6g.49458016T>CCA364404749MMUTc.428A>G (p.His143Arg)
gnomAD v4
6g.49458016T>GCA364404750MMUTc.428A>C (p.His143Pro)
6g.49458017_49458020delCA2578675210MMUTc.425_428del (p.Thr142IlefsTer?)
6g.49458017G>ACA364404751MMUTc.427C>T (p.His143Tyr)
gnomAD v4
6g.49458017G>CCA364404752MMUTc.427C>G (p.His143Asp)
6g.49458017G>TCA364404753MMUTc.427C>A (p.His143Asn)
6g.49458018delCA2573140887MMUTc.426del (p.His143IlefsTer?)
ClinVar dbSNP gnomAD v4
6g.49458018T>ACA450608688MMUTc.426A>T (p.Thr142=)
6g.49458018T>CCA450608689MMUTc.426A>G (p.Thr142=)
gnomAD v4
6g.49458018T>GCA450608690MMUTc.426A>C (p.Thr142=)
6g.49458019G>ACA364404754MMUTc.425C>T (p.Thr142Ile)
6g.49458019G>CCA364404755MMUTc.425C>G (p.Thr142Arg)
6g.49458019G>TCA364404756MMUTc.425C>A (p.Thr142Lys)
gnomAD v4
6g.49458020T>ACA364404759MMUTc.424A>T (p.Thr142Ser)
6g.49458020T>CCA364404758MMUTc.424A>G (p.Thr142Ala)
ClinVar
6g.49458020T>GCA364404757MMUTc.424A>C (p.Thr142Pro)
6g.49458021C>ACA450608691MMUTc.423G>T (p.Ala141=)
ClinVar dbSNP
6g.49458021C=CA1627395492MMUTc.423G= (p.Ala141=)
6g.49458021C>GCA450608692MMUTc.423G>C (p.Ala141=)
6g.49458021C>TCA3847111MMUTc.423G>A (p.Ala141=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49458021_49458022insAAACA2578675211MMUTc.422_423insTTT (p.Ala141_Thr142insLeu)
6g.49458022G>ACA3847112MMUTc.422C>T (p.Ala141Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
6g.49458022G>CCA364404760MMUTc.422C>G (p.Ala141Gly)
6g.49458022G=CA1627395501MMUTc.422C= (p.Ala141=)
6g.49458022G>TCA3847113MMUTc.422C>A (p.Ala141Glu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49458022_49458023delinsGCCA1627395509MMUTc.421_422delinsGC (p.Ala141=)
6g.49458023C>ACA364404761MMUTc.421G>T (p.Ala141Ser)
6g.49458023C=CA1627395521MMUTc.421G= (p.Ala141=)
6g.49458023C>GCA364404762MMUTc.421G>C (p.Ala141Pro)
6g.49458023C>TCA364404763MMUTc.421G>A (p.Ala141Thr)
ClinVar dbSNP
6g.49458024delCA1139659605MMUTc.421del (p.Ala141ArgfsTer?)
ClinVar dbSNP
6g.49458024C>ACA450608693MMUTc.420G>T (p.Leu140=)
6g.49458024C=CA1627395532MMUTc.420G= (p.Leu140=)
6g.49458024C>GCA450608694MMUTc.420G>C (p.Leu140=)
6g.49458024C>TCA3847114MMUTc.420G>A (p.Leu140=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49458025A>CCA364404764MMUTc.419T>G (p.Leu140Arg)
6g.49458025A>GCA364404765MMUTc.419T>C (p.Leu140Pro)
6g.49458025A>TCA364404766MMUTc.419T>A (p.Leu140Gln)
6g.49458026G>ACA450608695MMUTc.418C>T (p.Leu140=)
gnomAD v4
6g.49458026G>CCA364404767MMUTc.418C>G (p.Leu140Val)
6g.49458026G>TCA364404768MMUTc.418C>A (p.Leu140Met)
gnomAD v4
6g.49458027A>CCA364404770MMUTc.417T>G (p.Asp139Glu)
6g.49458027A>GCA450608696MMUTc.417T>C (p.Asp139=)
gnomAD v4
6g.49458027A>TCA364404769MMUTc.417T>A (p.Asp139Glu)
6g.49458028T>ACA364404771MMUTc.416A>T (p.Asp139Val)
6g.49458028T>CCA364404772MMUTc.416A>G (p.Asp139Gly)
6g.49458028T>GCA364404773MMUTc.416A>C (p.Asp139Ala)
6g.49458029C>ACA364404774MMUTc.415G>T (p.Asp139Tyr)
6g.49458029C=CA1627395536MMUTc.415G= (p.Asp139=)
6g.49458029C>GCA364404775MMUTc.415G>C (p.Asp139His)
6g.49458029C>TCA10575882MMUTc.415G>A (p.Asp139Asn)
ClinVar dbSNP
6g.49458030A>CCA364404777MMUTc.414T>G (p.Phe138Leu)
6g.49458030A>GCA450608697MMUTc.414T>C (p.Phe138=)
ClinVar dbSNP gnomAD v4
6g.49458030A>TCA364404776MMUTc.414T>A (p.Phe138Leu)
6g.49458030_49458048delinsGTGGCTTTATATATTCA2580075487MMUTc.396_414delinsAATATATAAAGCCAC (p.Gly133IlefsTer?)
ClinVar
6g.49458031A>CCA364404778MMUTc.413T>G (p.Phe138Cys)
6g.49458031A>GCA364404779MMUTc.413T>C (p.Phe138Ser)
6g.49458031A>TCA364404780MMUTc.413T>A (p.Phe138Tyr)
gnomAD v4
6g.49458032A>CCA364404781MMUTc.412T>G (p.Phe138Val)
6g.49458032A>GCA364404782MMUTc.412T>C (p.Phe138Leu)
6g.49458032A>TCA364404783MMUTc.412T>A (p.Phe138Ile)
6g.49458033G>ACA450608698MMUTc.411C>T (p.Ala137=)
6g.49458033G>CCA450608699MMUTc.411C>G (p.Ala137=)
6g.49458033G>TCA450608700MMUTc.411C>A (p.Ala137=)
6g.49458034G>ACA364404785MMUTc.410C>T (p.Ala137Val)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
6g.49458034G>CCA138800018MMUTc.410C>G (p.Ala137Gly)
ClinVar dbSNP
6g.49458034G=CA1627395545MMUTc.410C= (p.Ala137=)
6g.49458034G>TCA364404784MMUTc.410C>A (p.Ala137Asp)
6g.49458035C>ACA364404786MMUTc.409G>T (p.Ala137Ser)
6g.49458035C>GCA364404787MMUTc.409G>C (p.Ala137Pro)
6g.49458035C>TCA364404788MMUTc.409G>A (p.Ala137Thr)
6g.49458036A=CA1627395549MMUTc.408T= (p.Val136=)
6g.49458036A>CCA450608702MMUTc.408T>G (p.Val136=)
dbSNP gnomAD v2
6g.49458036A>GCA450608703MMUTc.408T>C (p.Val136=)
6g.49458036A>TCA450608701MMUTc.408T>A (p.Val136=)
6g.49458037A>CCA364404789MMUTc.407T>G (p.Val136Gly)
COSMIC
6g.49458037A>GCA364404790MMUTc.407T>C (p.Val136Ala)
6g.49458037A>TCA364404791MMUTc.407T>A (p.Val136Asp)
gnomAD v4
6g.49458038delCA2679047070MMUTc.406del (p.Val136LeufsTer?)
gnomAD v4
6g.49458038C>ACA364404792MMUTc.406G>T (p.Val136Phe)
ClinVar dbSNP
6g.49458038C=CA1627395556MMUTc.406G= (p.Val136=)
6g.49458038C>GCA364404793MMUTc.406G>C (p.Val136Leu)
6g.49458038C>TCA364404794MMUTc.406G>A (p.Val136Ile)
ClinVar dbSNP gnomAD v3 gnomAD v4
6g.49458039T>ACA450608706MMUTc.405A>T (p.Ser135=)
6g.49458039T>CCA450608705MMUTc.405A>G (p.Ser135=)
ClinVar dbSNP
6g.49458039T>GCA450608704MMUTc.405A>C (p.Ser135=)
6g.49458040G>ACA364404795MMUTc.404C>T (p.Ser135Leu)
ClinVar gnomAD v4
6g.49458040G>CCA364404796MMUTc.404C>G (p.Ser135Ter)
6g.49458040G>TCA364404797MMUTc.404C>A (p.Ser135Ter)
6g.49458041A>CCA364404798MMUTc.403T>G (p.Ser135Ala)
6g.49458041A>GCA364404800MMUTc.403T>C (p.Ser135Pro)
6g.49458041A>TCA364404799MMUTc.403T>A (p.Ser135Thr)
6g.49458042T>ACA364404801MMUTc.402A>T (p.Leu134Phe)
6g.49458042T>CCA450608707MMUTc.402A>G (p.Leu134=)
6g.49458042T>GCA364404802MMUTc.402A>C (p.Leu134Phe)
6g.49458043A=CA1627395565MMUTc.401T= (p.Leu134=)
6g.49458043A>CCA364404803MMUTc.401T>G (p.Leu134Ter)
6g.49458043A>GCA364404804MMUTc.401T>C (p.Leu134Ser)
6g.49458043A>TCA364404805MMUTc.401T>A (p.Leu134Ter)
ClinVar dbSNP
6g.49458044A=CA1627395571MMUTc.400T= (p.Leu134=)
6g.49458044A>CCA364404806MMUTc.400T>G (p.Leu134Val)
6g.49458044A>GCA450608708MMUTc.400T>C (p.Leu134=)
dbSNP
6g.49458044A>TCA364404807MMUTc.400T>A (p.Leu134Ile)
6g.49458045T>ACA450608709MMUTc.399A>T (p.Gly133=)
6g.49458045T>CCA450608710MMUTc.399A>G (p.Gly133=)
ClinVar dbSNP gnomAD v4
6g.49458045T>GCA450608711MMUTc.399A>C (p.Gly133=)
6g.49458045_49458046delCA2695206692MMUTc.398_399del (p.Gly133ValfsTer6)
6g.49458046C>ACA364404808MMUTc.398G>T (p.Gly133Val)
ClinVar
6g.49458046C>GCA364404809MMUTc.398G>C (p.Gly133Ala)
gnomAD v4
6g.49458046C>TCA364404810MMUTc.398G>A (p.Gly133Glu)
ClinVar dbSNP
6g.49458047C>ACA364404811MMUTc.397G>T (p.Gly133Ter)
ClinVar dbSNP
6g.49458047C=CA1627395575MMUTc.397G= (p.Gly133=)
6g.49458047C>GCA364404812MMUTc.397G>C (p.Gly133Arg)
6g.49458047C>TCA10575883MMUTc.397G>A (p.Gly133Arg)
ClinVar dbSNP gnomAD v4
6g.49458048C>ACA364404814MMUTc.396G>T (p.Gln132His)
6g.49458048C>GCA364404813MMUTc.396G>C (p.Gln132His)
6g.49458048C>TCA450608712MMUTc.396G>A (p.Gln132=)
ClinVar
6g.49458049T>ACA364404815MMUTc.395A>T (p.Gln132Leu)
ClinVar dbSNP gnomAD v4
6g.49458049T>CCA3847115MMUTc.395A>G (p.Gln132Arg)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49458049T>GCA364404816MMUTc.395A>C (p.Gln132Pro)
6g.49458049T=CA1627395583MMUTc.395A= (p.Gln132=)
6g.49458050G>ACA364404817MMUTc.394C>T (p.Gln132Ter)
ClinVar dbSNP gnomAD v4
6g.49458050G>CCA364404818MMUTc.394C>G (p.Gln132Glu)
6g.49458050G=CA1627395590MMUTc.394C= (p.Gln132=)
6g.49458050G>TCA364404819MMUTc.394C>A (p.Gln132Lys)
6g.49458051C>ACA364404820MMUTc.393G>T (p.Gln131His)
ClinVar
6g.49458051C=CA1627395595MMUTc.393G= (p.Gln131=)
6g.49458051C>GCA364404821MMUTc.393G>C (p.Gln131His)
6g.49458051C>TCA243129MMUTc.393G>A (p.Gln131=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49458052T>ACA3847116MMUTc.392A>T (p.Gln131Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.49458052T>CCA364404822MMUTc.392A>G (p.Gln131Arg)
6g.49458052T>GCA364404823MMUTc.392A>C (p.Gln131Pro)
6g.49458052T=CA1627395599MMUTc.392A= (p.Gln131=)
6g.49458053G>ACA364404825MMUTc.391C>T (p.Gln131Ter)
6g.49458053G>CCA364404826MMUTc.391C>G (p.Gln131Glu)
6g.49458053G>TCA364404824MMUTc.391C>A (p.Gln131Lys)
gnomAD v4
6g.49458054A>CCA450608713MMUTc.390T>G (p.Gly130=)
6g.49458054A>GCA450608714MMUTc.390T>C (p.Gly130=)
6g.49458054A>TCA450608715MMUTc.390T>A (p.Gly130=)
6g.49458055C>ACA364404827MMUTc.389G>T (p.Gly130Val)
6g.49458055C>GCA364404828MMUTc.389G>C (p.Gly130Ala)
6g.49458055C>TCA364404829MMUTc.389G>A (p.Gly130Asp)
gnomAD v4
6g.49458056C>ACA364404830MMUTc.388G>T (p.Gly130Cys)
gnomAD v4
6g.49458056C>GCA364404831MMUTc.388G>C (p.Gly130Arg)
6g.49458056C>TCA364404832MMUTc.388G>A (p.Gly130Ser)
6g.49458057A>CCA450608717MMUTc.387T>G (p.Ala129=)
6g.49458057A>GCA450608718MMUTc.387T>C (p.Ala129=)
6g.49458057A>TCA450608716MMUTc.387T>A (p.Ala129=)
6g.49458058G>ACA364404833MMUTc.386C>T (p.Ala129Val)
dbSNP gnomAD v2 gnomAD v4
6g.49458058G>CCA364404834MMUTc.386C>G (p.Ala129Gly)
6g.49458058G=CA1627395607MMUTc.386C= (p.Ala129=)
6g.49458058G>TCA364404835MMUTc.386C>A (p.Ala129Asp)
gnomAD v4
6g.49458059C>ACA364404836MMUTc.386-1G>T (n.386-1G>T)
6g.49458059C>GCA364404837MMUTc.386-1G>C (n.386-1G>C)
6g.49458059C>TCA364404838MMUTc.386-1G>A (n.386-1G>A)
ClinVar dbSNP
6g.49458060T>ACA364404840MMUTc.386-2A>T (n.386-2A>T)
6g.49458060T>CCA364404841MMUTc.386-2A>G (n.386-2A>G)
6g.49458060T>GCA364404839MMUTc.386-2A>C (n.386-2A>C)
6g.49458062A>CCA2740091362MMUTc.386-4T>G (n.386-4T>G)
ClinVar
6g.49458065A>GCA2499218334MMUTc.386-7T>C (n.386-7T>C)
ClinVar dbSNP gnomAD v4
6g.49458066T>ACA2679047088MMUTc.386-8A>T (n.386-8A>T)
gnomAD v4
6g.49458066T>CCA1627395610MMUTc.386-8A>G (n.386-8A>G)
dbSNP gnomAD v4
6g.49458066T=CA1627395611MMUTc.386-8A= (n.386-8A=)
6g.49458067A=CA1627395613MMUTc.386-9T= (n.386-9T=)
6g.49458067A>GCA567155979MMUTc.386-9T>C (n.386-9T>C)
dbSNP gnomAD v2 gnomAD v4
6g.49458068T>CCA2580075490MMUTc.386-10A>G (n.386-10A>G)
ClinVar
6g.49458069_49458072delinsAAAGCA1627395616MMUTc.386-14_386-11delinsCTTT (n.386-14_386-11delinsCTTT)
6g.49458070A=CA1627395619MMUTc.386-12T= (n.386-12T=)
6g.49458070A>CCA567155980MMUTc.386-12T>G (n.386-12T>G)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.49458070A>GCA2711532910MMUTc.386-12T>C (n.386-12T>C)
dbSNP
6g.49458072_49458074delCA1627395618MMUTc.386-14_386-12del (n.386-14_386-12del)
dbSNP
6g.49458072G>ACA650898858MMUTc.386-14C>T (n.386-14C>T)
COSMIC
6g.49458072G=CA1627395621MMUTc.386-14C= (n.386-14C=)
6g.49458072G>TCA2516811258MMUTc.386-14C>A (n.386-14C>A)
ClinVar
6g.49458077_49458078insAAAAAAAACA1627395623MMUTc.386-15_386-14insTTTTTTTT (n.386-15_386-14insTTTTTTTT)
dbSNP
6g.49458074A=CA1627395625MMUTc.386-16T= (n.386-16T=)
6g.49458074A>CCA3847117MMUTc.386-16T>G (n.386-16T>G)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.49458076A=CA1627395626MMUTc.386-18T= (n.386-18T=)
6g.49458076A>CCA138800083MMUTc.386-18T>G (n.386-18T>G)
dbSNP

Number of alleles fetched