Primary Site >> Stomach Cancer

Gene >> CD226

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000280200
Start 69896003:69896003(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375997671
CDS Mutation c.425C>T
AA Mutation p.Ser142Leu(p.S142L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000280200
Start 69895961:69895961(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.467T>C
AA Mutation p.Met156Thr(p.M156T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000280200
Start 69895828:69895828(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.600C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000280200
Start 69895729:69895729(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.699C>G
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000280200
Start 69895735:69895735(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs192778937
CDS Mutation c.693C>T
Mutation Classification Silent
Feature Type Transcript