Primary Site >> Stomach Cancer

Gene >> HCCS

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000321143
Start 11117277:11117277(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.263C>A
AA Mutation p.Pro88Gln(p.P88Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000321143
Start 11118517:11118517(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.418G>A
AA Mutation p.Glu140Lys(p.E140K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000321143
Start 11114928:11114928(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.194A>C
AA Mutation p.Glu65Ala(p.E65A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000321143
Start 11120975:11120975(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776172899
CDS Mutation c.590G>A
AA Mutation p.Arg197Gln(p.R197Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000321143
Start 11114932:11114932(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.198T>C
Mutation Classification Silent
Feature Type Transcript