Primary Site >> Stomach Cancer

Gene >> TMPRSS2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000332149
Start 41489528:41489528(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.304G>A
AA Mutation p.Ala102Thr(p.A102T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000332149
Start 41480578:41480578(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.470T>G
AA Mutation p.Ile157Ser(p.I157S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000332149
Start 41468515:41468515(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs185312677
CDS Mutation c.1195G>A
AA Mutation p.Ala399Thr(p.A399T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000332149
Start 41494437:41494437(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753509316
CDS Mutation c.157G>A
AA Mutation p.Ala53Thr(p.A53T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000332149
Start 41494393:41494393(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.201G>A
Mutation Classification Silent
Feature Type Transcript