Primary Site >> Stomach Cancer

Gene >> CD4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000011653
Start 6814204:6814204(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.277C>A
AA Mutation p.Pro93Thr(p.P93T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000011653
Start 6816157:6816157(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.709G>A
AA Mutation p.Glu237Lys(p.E237K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000011653
Start 6814213:6814213(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.286A>G
AA Mutation p.Ile96Val(p.I96V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000011653
Start 6816257:6816257(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.809C>A
AA Mutation p.Pro270His(p.P270H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000011653
Start 6816145:6816145(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.697A>T
AA Mutation p.Thr233Ser(p.T233S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000011653
Start 6814793:6814793(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.408G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000011653
Start 6817263:6817263(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1089T>C
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000011653
Start 6819323:6819323(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1371C>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000011653
Start 6800311:6800311(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.54C>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000011653
Start 6814877:6814877(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.498delG
AA Mutation p.Lys167ArgfsTer31(p.K167Rfs*31)
Mutation Classification Frame_Shift_Del
Feature Type Transcript