Primary Site >> Stomach Cancer

Gene >> CTSS

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368985
Start 150764750:150764750(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.14T>C
AA Mutation p.Val5Ala(p.V5A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000368985
Start 150751813:150751813(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775224994
CDS Mutation c.595G>A
AA Mutation p.Asp199Asn(p.D199N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000368985
Start 150750015:150750015(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.784T>C
AA Mutation p.Tyr262His(p.Y262H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000368985
Start 150750033:150750033(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.766C>T
AA Mutation p.His256Tyr(p.H256Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000368985
Start 150751837:150751837(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.571T>C
AA Mutation p.Tyr191His(p.Y191H)
Mutation Classification Missense_Mutation
Feature Type Transcript