Primary Site >> Esophagus Cancer

Gene >> ARID1A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000324856
Start 26780157:26780157(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6259G>A
AA Mutation p.Gly2087Arg(p.G2087R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000324856
Start 26762273:26762273(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2373C>A
AA Mutation p.Asn791Lys(p.N791K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000324856
Start 26731177:26731177(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1376C>T
AA Mutation p.Pro459Leu(p.P459L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000324856
Start 26761388:26761388(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2166C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000324856
Start 26774868:26774868(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4641C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000324856
Start 26762191:26762191(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2296delC
AA Mutation p.Gln766SerfsTer67(p.Q766Sfs*67)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000324856
Start 26780425:26780425(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.6527delA
AA Mutation p.Gln2176ArgfsTer24(p.Q2176Rfs*24)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000324856
Start 26760926:26760926(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1991delC
AA Mutation p.Ser664Ter(p.S664*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000324856
Start 26731443:26731443(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1642C>T
AA Mutation p.Gln548Ter(p.Q548*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000324856
Start 26773833:26773833(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4036C>T
AA Mutation p.Gln1346Ter(p.Q1346*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000324856
Start 26779578:26779578(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5680C>T
AA Mutation p.Gln1894Ter(p.Q1894*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000324856
Start 26731481:26731481(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1680C>A
AA Mutation p.Tyr560Ter(p.Y560*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence stop_gained
Transcription ID ENST00000324856
Start 26774761:26774761(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4534C>T
AA Mutation p.Gln1512Ter(p.Q1512*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000324856
Start 26771130:26771131(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.3216dupA
AA Mutation p.Trp1073MetfsTer32(p.W1073Mfs*32)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000324856
Start 26780479:26780480(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.6583dupC
AA Mutation p.Leu2195ProfsTer30(p.L2195Pfs*30)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000324856
Start 26763040:26763041(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2489dupG
AA Mutation p.Gly831ArgfsTer41(p.G831Rfs*41)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000324856
Start 26772970:26772971(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.3699_3700dupTG
AA Mutation p.Gly1234ValfsTer4(p.G1234Vfs*4)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript