Primary Site >> Stomach Cancer

Gene >> TMEM25

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000313236
Start 118532180:118532180(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.101G>A
AA Mutation p.Gly34Asp(p.G34D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000313236
Start 118532974:118532974(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.440T>A
AA Mutation p.Leu147His(p.L147H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000313236
Start 118533133:118533133(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377765778
CDS Mutation c.599G>A
AA Mutation p.Arg200His(p.R200H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000313236
Start 118532970:118532970(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.436G>T
AA Mutation p.Gly146Cys(p.G146C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000313236
Start 118534066:118534066(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.874C>T
AA Mutation p.Pro292Ser(p.P292S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000313236
Start 118532290:118532290(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.211C>T
Mutation Classification Silent
Feature Type Transcript