Primary Site >> Stomach Cancer

Gene >> IFNGR1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000367739
Start 137219281:137219281(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.47G>A
AA Mutation p.Arg16Lys(p.R16K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000367739
Start 137200982:137200982(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.760G>A
AA Mutation p.Ala254Thr(p.A254T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000367739
Start 137203574:137203574(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.658G>C
AA Mutation p.Val220Leu(p.V220L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000367739
Start 137198585:137198585(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.916T>C
AA Mutation p.Ser306Pro(p.S306P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000367739
Start 137206998:137206998(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.165G>T
AA Mutation p.Gln55His(p.Q55H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000367739
Start 137204474:137204474(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.404G>A
AA Mutation p.Arg135Lys(p.R135K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000367739
Start 137204420:137204420(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.458A>G
AA Mutation p.Asn153Ser(p.N153S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000367739
Start 137198448:137198448(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1053T>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000367739
Start 137207073:137207073(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.90T>C
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000367739
Start 137203535:137203536(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.696dupA
AA Mutation p.Glu233ArgfsTer9(p.E233Rfs*9)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000367739
Start 137206181:137206182(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.327dupA
AA Mutation p.Glu110ArgfsTer22(p.E110Rfs*22)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript