Primary Site >> Stomach Cancer

Gene >> CXCL9

ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000264888
Start 76004809:76004809(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.276G>T
AA Mutation p.Gln92His(p.Q92H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264888
Start 76003635:76003635(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139830877
CDS Mutation c.341G>A
AA Mutation p.Arg114Gln(p.R114Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000264888
Start 76006240:76006240(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377485242
CDS Mutation c.99C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000264888
Start 76003673:76003673(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.303T>C
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000264888
Start 76003663:76003664(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.312dupA
AA Mutation p.His105ThrfsTer51(p.H105Tfs*51)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript