Primary Site >> Stomach Cancer

Gene >> CTAG2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000247306
Start 154653253:154653253(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.263T>A
AA Mutation p.Leu88His(p.L88H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000247306
Start 154652354:154652354(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.547C>T
AA Mutation p.Pro183Ser(p.P183S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000247306
Start 154652422:154652422(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.479C>T
AA Mutation p.Pro160Leu(p.P160L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000247306
Start 154652429:154652429(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199533324
CDS Mutation c.472G>A
AA Mutation p.Ala158Thr(p.A158T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000247306
Start 154652538:154652538(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.363G>A
Mutation Classification Silent
Feature Type Transcript