Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.79983913C>ACA16604726ANTXR2c.1144G>T (p.Gly382Cys)
c.913G>T (p.Gly305Cys)
c.835G>T (p.Gly279Cys)
c.*294G>T (n.*294G>T)
ClinVar dbSNP
4g.79983913C=CA1471254589ANTXR2c.1144G= (p.Gly382=)
c.913G= (p.Gly305=)
c.835G= (p.Gly279=)
c.*294G= (n.*294G=)
4g.79983913C>GCA357471461ANTXR2c.1144G>C (p.Gly382Arg)
c.913G>C (p.Gly305Arg)
c.835G>C (p.Gly279Arg)
c.*294G>C (n.*294G>C)
4g.79983913C>TCA357471460ANTXR2c.1144G>A (p.Gly382Ser)
c.913G>A (p.Gly305Ser)
c.835G>A (p.Gly279Ser)
c.*294G>A (n.*294G>A)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.79983914A>CCA357471462ANTXR2c.1143T>G (p.Tyr381Ter)
c.912T>G (p.Tyr304Ter)
c.834T>G (p.Tyr278Ter)
c.*293T>G (n.*293T>G)
4g.79983914A>GCA440062320ANTXR2c.1143T>C (p.Tyr381=)
c.912T>C (p.Tyr304=)
c.834T>C (p.Tyr278=)
c.*293T>C (n.*293T>C)
4g.79983914A>TCA357471463ANTXR2c.1143T>A (p.Tyr381Ter)
c.912T>A (p.Tyr304Ter)
c.834T>A (p.Tyr278Ter)
c.*293T>A (n.*293T>A)
4g.79983915T>ACA2981694ANTXR2c.1142A>T (p.Tyr381Phe)
c.911A>T (p.Tyr304Phe)
c.833A>T (p.Tyr278Phe)
c.*292A>T (n.*292A>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.79983915T>CCA252343ANTXR2c.1142A>G (p.Tyr381Cys)
c.911A>G (p.Tyr304Cys)
c.833A>G (p.Tyr278Cys)
c.*292A>G (n.*292A>G)
ClinVar dbSNP
4g.79983915T>GCA357471464ANTXR2c.1142A>C (p.Tyr381Ser)
c.911A>C (p.Tyr304Ser)
c.833A>C (p.Tyr278Ser)
c.*292A>C (n.*292A>C)
4g.79983915T=CA1471254594ANTXR2c.1142A= (p.Tyr381=)
c.911A= (p.Tyr304=)
c.833A= (p.Tyr278=)
c.*292A= (n.*292A=)
4g.79983916A>CCA357471465ANTXR2c.1141T>G (p.Tyr381Asp)
c.910T>G (p.Tyr304Asp)
c.832T>G (p.Tyr278Asp)
c.*291T>G (n.*291T>G)
4g.79983916A>GCA357471466ANTXR2c.1141T>C (p.Tyr381His)
c.910T>C (p.Tyr304His)
c.832T>C (p.Tyr278His)
c.*291T>C (n.*291T>C)
4g.79983916A>TCA357471467ANTXR2c.1141T>A (p.Tyr381Asn)
c.910T>A (p.Tyr304Asn)
c.832T>A (p.Tyr278Asn)
c.*291T>A (n.*291T>A)
gnomAD v4
4g.79983917A>CCA357471468ANTXR2c.1140T>G (p.Tyr380Ter)
c.909T>G (p.Tyr303Ter)
c.831T>G (p.Tyr277Ter)
c.*290T>G (n.*290T>G)
4g.79983917A>GCA440062321ANTXR2c.1140T>C (p.Tyr380=)
c.909T>C (p.Tyr303=)
c.831T>C (p.Tyr277=)
c.*290T>C (n.*290T>C)
4g.79983917A>TCA357471469ANTXR2c.1140T>A (p.Tyr380Ter)
c.909T>A (p.Tyr303Ter)
c.831T>A (p.Tyr277Ter)
c.*290T>A (n.*290T>A)
4g.79983918delCA2582342654ANTXR2c.1139del (p.Tyr380PhefsTer29)
c.908del (p.Tyr303PhefsTer29)
c.830del (p.Tyr277PhefsTer29)
c.*289del (n.*289del)
ClinVar
4g.79983918T>ACA357471470ANTXR2c.1139A>T (p.Tyr380Phe)
c.908A>T (p.Tyr303Phe)
c.830A>T (p.Tyr277Phe)
c.*289A>T (n.*289A>T)
4g.79983918T>CCA357471471ANTXR2c.1139A>G (p.Tyr380Cys)
c.908A>G (p.Tyr303Cys)
c.830A>G (p.Tyr277Cys)
c.*289A>G (n.*289A>G)
4g.79983918T>GCA357471472ANTXR2c.1139A>C (p.Tyr380Ser)
c.908A>C (p.Tyr303Ser)
c.830A>C (p.Tyr277Ser)
c.*289A>C (n.*289A>C)
4g.79983919A>CCA357471474ANTXR2c.1138T>G (p.Tyr380Asp)
c.907T>G (p.Tyr303Asp)
c.829T>G (p.Tyr277Asp)
c.*288T>G (n.*288T>G)
4g.79983919A>GCA357471475ANTXR2c.1138T>C (p.Tyr380His)
c.907T>C (p.Tyr303His)
c.829T>C (p.Tyr277His)
c.*288T>C (n.*288T>C)
gnomAD v4
4g.79983919A>TCA357471473ANTXR2c.1138T>A (p.Tyr380Asn)
c.907T>A (p.Tyr303Asn)
c.829T>A (p.Tyr277Asn)
c.*288T>A (n.*288T>A)
4g.79983920G>ACA440062322ANTXR2c.1137C>T (p.Ser379=)
c.906C>T (p.Ser302=)
c.828C>T (p.Ser276=)
c.*287C>T (n.*287C>T)
4g.79983920G>CCA440062324ANTXR2c.1137C>G (p.Ser379=)
c.906C>G (p.Ser302=)
c.828C>G (p.Ser276=)
c.*287C>G (n.*287C>G)
4g.79983920G>TCA440062323ANTXR2c.1137C>A (p.Ser379=)
c.906C>A (p.Ser302=)
c.828C>A (p.Ser276=)
c.*287C>A (n.*287C>A)
4g.79983921G>ACA357471476ANTXR2c.1136C>T (p.Ser379Phe)
c.905C>T (p.Ser302Phe)
c.827C>T (p.Ser276Phe)
c.*286C>T (n.*286C>T)
4g.79983921G>CCA357471478ANTXR2c.1136C>G (p.Ser379Cys)
c.905C>G (p.Ser302Cys)
c.827C>G (p.Ser276Cys)
c.*286C>G (n.*286C>G)
4g.79983921G>TCA357471477ANTXR2c.1136C>A (p.Ser379Tyr)
c.905C>A (p.Ser302Tyr)
c.827C>A (p.Ser276Tyr)
c.*286C>A (n.*286C>A)
4g.79983922A>CCA357471479ANTXR2c.1135T>G (p.Ser379Ala)
c.904T>G (p.Ser302Ala)
c.826T>G (p.Ser276Ala)
c.*285T>G (n.*285T>G)
4g.79983922A>GCA357471481ANTXR2c.1135T>C (p.Ser379Pro)
c.904T>C (p.Ser302Pro)
c.826T>C (p.Ser276Pro)
c.*285T>C (n.*285T>C)
gnomAD v4
4g.79983922A>TCA357471480ANTXR2c.1135T>A (p.Ser379Thr)
c.904T>A (p.Ser302Thr)
c.826T>A (p.Ser276Thr)
c.*285T>A (n.*285T>A)
4g.79983923A=CA1471254599ANTXR2c.1134T= (p.Ala378=)
c.903T= (p.Ala301=)
c.825T= (p.Ala275=)
c.*284T= (n.*284T=)
4g.79983923A>CCA440062325ANTXR2c.1134T>G (p.Ala378=)
c.903T>G (p.Ala301=)
c.825T>G (p.Ala275=)
c.*284T>G (n.*284T>G)
4g.79983923A>GCA440062326ANTXR2c.1134T>C (p.Ala378=)
c.903T>C (p.Ala301=)
c.825T>C (p.Ala275=)
c.*284T>C (n.*284T>C)
dbSNP gnomAD v2 gnomAD v4
4g.79983923A>TCA440062327ANTXR2c.1134T>A (p.Ala378=)
c.903T>A (p.Ala301=)
c.825T>A (p.Ala275=)
c.*284T>A (n.*284T>A)
4g.79983924G>ACA357471482ANTXR2c.1133C>T (p.Ala378Val)
c.902C>T (p.Ala301Val)
c.824C>T (p.Ala275Val)
c.*283C>T (n.*283C>T)
gnomAD v4
4g.79983924G>CCA357471483ANTXR2c.1133C>G (p.Ala378Gly)
c.902C>G (p.Ala301Gly)
c.824C>G (p.Ala275Gly)
c.*283C>G (n.*283C>G)
4g.79983924G>TCA357471484ANTXR2c.1133C>A (p.Ala378Asp)
c.902C>A (p.Ala301Asp)
c.824C>A (p.Ala275Asp)
c.*283C>A (n.*283C>A)
COSMIC COSMIC
4g.79983925C>ACA357471485ANTXR2c.1132G>T (p.Ala378Ser)
c.901G>T (p.Ala301Ser)
c.823G>T (p.Ala275Ser)
c.*282G>T (n.*282G>T)
4g.79983925C>GCA357471486ANTXR2c.1132G>C (p.Ala378Pro)
c.901G>C (p.Ala301Pro)
c.823G>C (p.Ala275Pro)
c.*282G>C (n.*282G>C)
4g.79983925C>TCA357471487ANTXR2c.1132G>A (p.Ala378Thr)
c.901G>A (p.Ala301Thr)
c.823G>A (p.Ala275Thr)
c.*282G>A (n.*282G>A)
4g.79983926A>CCA357471488ANTXR2c.1131T>G (p.Asp377Glu)
c.900T>G (p.Asp300Glu)
c.822T>G (p.Asp274Glu)
c.*281T>G (n.*281T>G)
4g.79983926A>GCA440062328ANTXR2c.1131T>C (p.Asp377=)
c.900T>C (p.Asp300=)
c.822T>C (p.Asp274=)
c.*281T>C (n.*281T>C)
4g.79983926A>TCA357471489ANTXR2c.1131T>A (p.Asp377Glu)
c.900T>A (p.Asp300Glu)
c.822T>A (p.Asp274Glu)
c.*281T>A (n.*281T>A)
4g.79983927T>ACA357471490ANTXR2c.1130A>T (p.Asp377Val)
c.899A>T (p.Asp300Val)
c.821A>T (p.Asp274Val)
c.*280A>T (n.*280A>T)
COSMIC
4g.79983927T>CCA357471491ANTXR2c.1130A>G (p.Asp377Gly)
c.899A>G (p.Asp300Gly)
c.821A>G (p.Asp274Gly)
c.*280A>G (n.*280A>G)
4g.79983927T>GCA357471492ANTXR2c.1130A>C (p.Asp377Ala)
c.899A>C (p.Asp300Ala)
c.821A>C (p.Asp274Ala)
c.*280A>C (n.*280A>C)
4g.79983928C>ACA357471493ANTXR2c.1129G>T (p.Asp377Tyr)
c.898G>T (p.Asp300Tyr)
c.820G>T (p.Asp274Tyr)
c.*279G>T (n.*279G>T)
dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched