Primary Site >> Stomach Cancer

Gene >> ANO5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000324559
Start 22250809:22250809(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1082A>T
AA Mutation p.Asp361Val(p.D361V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000324559
Start 22236197:22236197(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.683T>C
AA Mutation p.Ile228Thr(p.I228T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000324559
Start 22279566:22279566(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2543T>G
AA Mutation p.Phe848Cys(p.F848C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000324559
Start 22236253:22236253(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.739T>A
AA Mutation p.Ser247Thr(p.S247T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000324559
Start 22270334:22270334(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372674175
CDS Mutation c.1921C>T
AA Mutation p.Arg641Cys(p.R641C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000324559
Start 22259531:22259531(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750702622
CDS Mutation c.1420G>A
AA Mutation p.Val474Ile(p.V474I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000324559
Start 22272847:22272847(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2093T>C
AA Mutation p.Leu698Pro(p.L698P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000324559
Start 22236215:22236215(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749374398
CDS Mutation c.701G>A
AA Mutation p.Arg234Lys(p.R234K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000324559
Start 22272955:22272955(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2201T>G
AA Mutation p.Leu734Arg(p.L734R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000324559
Start 22227308:22227308(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.370G>A
AA Mutation p.Glu124Lys(p.E124K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000324559
Start 22250336:22250336(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.978T>G
AA Mutation p.Ile326Met(p.I326M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000324559
Start 22211287:22211287(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.111C>G
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000324559
Start 22221101:22221101(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.191delA
AA Mutation p.Asn64IlefsTer27(p.N64Ifs*27)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000324559
Start 22255379:22255379(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1193delT
AA Mutation p.Leu398TrpfsTer29(p.L398Wfs*29)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence stop_gained
Transcription ID ENST00000324559
Start 22270436:22270436(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2023G>T
AA Mutation p.Glu675Ter(p.E675*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence splice_donor_variant
Transcription ID ENST00000324559
Start 22263045:22263045(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1898+2T>C
Mutation Classification Splice_Site
Feature Type Transcript