Primary Site >> Stomach Cancer

Gene >> HLA-G

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000360323
Start 29828185:29828185(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.212C>T
AA Mutation p.Pro71Leu(p.P71L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000360323
Start 29828217:29828217(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.244G>A
AA Mutation p.Glu82Lys(p.E82K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000360323
Start 29828149:29828149(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.176G>A
AA Mutation p.Arg59Gln(p.R59Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000360323
Start 29828210:29828210(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.237G>T
AA Mutation p.Glu79Asp(p.E79D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000360323
Start 29828743:29828743(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.544G>A
AA Mutation p.Ala182Thr(p.A182T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000360323
Start 29828673:29828673(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.474C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000360323
Start 29828138:29828138(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.165G>A
Mutation Classification Silent
Feature Type Transcript