Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.50625960dupCA916083827ARSAc.1087dup (p.Leu363ProfsTer?)
c.829dup (p.Leu277ProfsTer?)
ClinVar dbSNP
22g.50625960delCA645612057ARSAc.1087del (p.Leu363CysfsTer?)
c.829del (p.Leu277CysfsTer?)
c.1087del (p.Leu363CysfsTer12)
COSMIC
22g.50625957G>ACA515248839ARSAc.1086C>T (p.Pro362=)
c.828C>T (p.Pro276=)
ClinVar dbSNP gnomAD v3 gnomAD v4
22g.50625957G>CCA515248840ARSAc.1086C>G (p.Pro362=)
c.828C>G (p.Pro276=)
22g.50625957G=CA2410958756ARSAc.1086C= (p.Pro362=)
c.828C= (p.Pro276=)
22g.50625957G>TCA515248841ARSAc.1086C>A (p.Pro362=)
c.828C>A (p.Pro276=)
gnomAD v4
22g.50625958G>ACA412171348ARSAc.1085C>T (p.Pro362Leu)
c.827C>T (p.Pro276Leu)
22g.50625958G>CCA412171349ARSAc.1085C>G (p.Pro362Arg)
c.827C>G (p.Pro276Arg)
dbSNP gnomAD v2 gnomAD v4
22g.50625958G=CA2410958757ARSAc.1085C= (p.Pro362=)
c.827C= (p.Pro276=)
22g.50625958G>TCA412171353ARSAc.1085C>A (p.Pro362His)
c.827C>A (p.Pro276His)
gnomAD v4
22g.50625959G>ACA412171363ARSAc.1084C>T (p.Pro362Ser)
c.826C>T (p.Pro276Ser)
22g.50625959G>CCA412171383ARSAc.1084C>G (p.Pro362Ala)
c.826C>G (p.Pro276Ala)
22g.50625959G>TCA412171396ARSAc.1084C>A (p.Pro362Thr)
c.826C>A (p.Pro276Thr)
22g.50625959_50625961delinsGGCCA2410958758ARSAc.1082_1084delinsGCC (p.Ser361=)
c.824_826delinsGCC (p.Ser275=)
22g.50625960G>ACA515248842ARSAc.1083C>T (p.Ser361=)
c.825C>T (p.Ser275=)
22g.50625960G>CCA412171398ARSAc.1083C>G (p.Ser361Arg)
c.825C>G (p.Ser275Arg)
22g.50625960G=CA2410958759ARSAc.1083C= (p.Ser361=)
c.825C= (p.Ser275=)
22g.50625960G>TCA412171402ARSAc.1083C>A (p.Ser361Arg)
c.825C>A (p.Ser275Arg)
dbSNP gnomAD v4
22g.50625960_50625961delCA2410958760ARSAc.1082_1083del (p.Ser361ThrfsTer?)
c.824_825del (p.Ser275ThrfsTer?)
dbSNP
22g.50625961C>ACA412171417ARSAc.1082G>T (p.Ser361Ile)
c.824G>T (p.Ser275Ile)
gnomAD v4
22g.50625961C=CA2410958761ARSAc.1082G= (p.Ser361=)
c.824G= (p.Ser275=)
22g.50625961C>GCA412171428ARSAc.1082G>C (p.Ser361Thr)
c.824G>C (p.Ser275Thr)
22g.50625961C>TCA412171407ARSAc.1082G>A (p.Ser361Asn)
c.824G>A (p.Ser275Asn)
dbSNP
22g.50625962T>ACA412171433ARSAc.1081A>T (p.Ser361Cys)
c.823A>T (p.Ser275Cys)
22g.50625962T>CCA412171430ARSAc.1081A>G (p.Ser361Gly)
c.823A>G (p.Ser275Gly)
22g.50625962T>GCA412171431ARSAc.1081A>C (p.Ser361Arg)
c.823A>C (p.Ser275Arg)
22g.50625963G>ACA515248845ARSAc.1080C>T (p.Leu360=)
c.822C>T (p.Leu274=)
gnomAD v4
22g.50625963G>CCA515248843ARSAc.1080C>G (p.Leu360=)
c.822C>G (p.Leu274=)
22g.50625963G>TCA515248844ARSAc.1080C>A (p.Leu360=)
c.822C>A (p.Leu274=)
22g.50625964A=CA2410958763ARSAc.1079T= (p.Leu360=)
c.821T= (p.Leu274=)
22g.50625964A>CCA412171437ARSAc.1079T>G (p.Leu360Arg)
c.821T>G (p.Leu274Arg)
22g.50625964A>GCA412171445ARSAc.1079T>C (p.Leu360Pro)
c.821T>C (p.Leu274Pro)
ClinVar dbSNP
22g.50625964A>TCA412171448ARSAc.1079T>A (p.Leu360His)
c.821T>A (p.Leu274His)
22g.50625964_50625965delinsAGCA2410958762ARSAc.1078_1079delinsCT (p.Leu360=)
c.820_821delinsCT (p.Leu274=)
22g.50625965G>ACA412171454ARSAc.1078C>T (p.Leu360Phe)
c.820C>T (p.Leu274Phe)
22g.50625965G>CCA412171466ARSAc.1078C>G (p.Leu360Val)
c.820C>G (p.Leu274Val)
gnomAD v4
22g.50625965G=CA2410958765ARSAc.1078C= (p.Leu360=)
c.820C= (p.Leu274=)
22g.50625965G>TCA412171469ARSAc.1078C>A (p.Leu360Ile)
c.820C>A (p.Leu274Ile)
dbSNP gnomAD v4
22g.50625966delCA920392348ARSAc.1078del (p.Leu360SerfsTer?)
c.820del (p.Leu274SerfsTer?)
c.1078del (p.Leu360SerfsTer15)
dbSNP
22g.50625965_50625967delinsGGTCA2410958764ARSAc.1076_1078delinsACC (p.Asp359=)
c.818_820delinsACC (p.Asp273=)
22g.50625966G>ACA325531311ARSAc.1077C>T (p.Asp359=)
c.819C>T (p.Asp273=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
22g.50625966G>CCA412171472ARSAc.1077C>G (p.Asp359Glu)
c.819C>G (p.Asp273Glu)
22g.50625966G=CA2410958766ARSAc.1077C= (p.Asp359=)
c.819C= (p.Asp273=)
22g.50625966G>TCA412171476ARSAc.1077C>A (p.Asp359Glu)
c.819C>A (p.Asp273Glu)
22g.50625966_50625967delCA754068402ARSAc.1076_1077del (p.Asp359AlafsTer?)
c.818_819del (p.Asp273AlafsTer?)
dbSNP gnomAD v3 gnomAD v4
22g.50625967T>ACA412171489ARSAc.1076A>T (p.Asp359Val)
c.818A>T (p.Asp273Val)
22g.50625967T>CCA412171493ARSAc.1076A>G (p.Asp359Gly)
c.818A>G (p.Asp273Gly)
gnomAD v4
22g.50625967T>GCA412171495ARSAc.1076A>C (p.Asp359Ala)
c.818A>C (p.Asp273Ala)
22g.50625968C>ACA412171499ARSAc.1075G>T (p.Asp359Tyr)
c.817G>T (p.Asp273Tyr)
dbSNP gnomAD v2 gnomAD v4
22g.50625968C=CA2410958767ARSAc.1075G= (p.Asp359=)
c.817G= (p.Asp273=)

Number of alleles fetched