Primary Site >> Stomach Cancer

Gene >> IREB2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000258886
Start 78465277:78465277(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.299C>T
AA Mutation p.Ala100Val(p.A100V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000258886
Start 78487794:78487794(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746547492
CDS Mutation c.1771G>A
AA Mutation p.Ala591Thr(p.A591T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000258886
Start 78485740:78485740(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755226126
CDS Mutation c.1609C>T
AA Mutation p.Arg537Cys(p.R537C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000258886
Start 78439800:78439800(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.25G>A
AA Mutation p.Ala9Thr(p.A9T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000258886
Start 78465345:78465345(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.367G>T
AA Mutation p.Asp123Tyr(p.D123Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000258886
Start 78484908:78484908(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs553171458
CDS Mutation c.1561A>G
AA Mutation p.Met521Val(p.M521V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000258886
Start 78498130:78498130(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375120202
CDS Mutation c.2879G>A
AA Mutation p.Arg960Gln(p.R960Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000258886
Start 78439860:78439860(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.85T>C
AA Mutation p.Ser29Pro(p.S29P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000258886
Start 78439870:78439870(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.95G>A
AA Mutation p.Gly32Asp(p.G32D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000258886
Start 78476304:78476304(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1140T>C
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000258886
Start 78476205:78476205(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1041A>G
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000258886
Start 78471752:78471752(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.711A>G
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000258886
Start 78470568:78470568(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199867160
CDS Mutation c.666C>T
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000258886
Start 78484792:78484792(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1449delA
AA Mutation p.Lys483AsnfsTer60(p.K483Nfs*60)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000258886
Start 78470593:78470593(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.696delT
AA Mutation p.Phe232LeufsTer13(p.F232Lfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000258886
Start 78462966:78462966(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.151C>T
AA Mutation p.Arg51Ter(p.R51*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence stop_gained
Transcription ID ENST00000258886
Start 78478356:78478356(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1255C>T
AA Mutation p.Arg419Ter(p.R419*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript