Primary Site >> Stomach Cancer

Gene >> CTSF

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000310325
Start 66568009:66568009(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.287G>A
AA Mutation p.Arg96Gln(p.R96Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000310325
Start 66567304:66567304(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.549G>A
AA Mutation p.Met183Ile(p.M183I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000310325
Start 66563949:66563949(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs397514733
CDS Mutation c.1439C>T
AA Mutation p.Ser480Leu(p.S480L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000310325
Start 66565894:66565894(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.901A>T
AA Mutation p.Thr301Ser(p.T301S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000310325
Start 66564749:66564749(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1223G>A
AA Mutation p.Gly408Asp(p.G408D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000310325
Start 66567601:66567601(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.374G>A
AA Mutation p.Gly125Asp(p.G125D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000310325
Start 66564957:66564957(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1095C>A
Mutation Classification Silent
Feature Type Transcript