Primary Site >> Stomach Cancer

Gene >> CTSB

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000345125
Start 11853352:11853352(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.103A>G
AA Mutation p.Asn35Asp(p.N35D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000345125
Start 11852641:11852641(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.181A>G
AA Mutation p.Thr61Ala(p.T61A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000345125
Start 11847815:11847815(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.540A>G
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000345125
Start 11845152:11845152(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764030312
CDS Mutation c.993C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000345125
Start 11845707:11845707(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.876C>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000345125
Start 11845779:11845779(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.804delA
AA Mutation p.Gln268HisfsTer7(p.Q268Hfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript