Mutation

Primary Site >> Stomach Cancer

Gene >> TNFRSF8

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263932
Start	12138329:12138329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1436A>G
AA Mutation	p.Tyr479Cys(p.Y479C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263932
Start	12110124:12110124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749228869
CDS Mutation	c.596G>A
AA Mutation	p.Arg199His(p.R199H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263932
Start	12084540:12084540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757905742
CDS Mutation	c.140G>A
AA Mutation	p.Arg47His(p.R47H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263932
Start	12084489:12084489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.89A>T
AA Mutation	p.His30Leu(p.H30L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263932
Start	12110118:12110118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.590G>A
AA Mutation	p.Gly197Asp(p.G197D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263932
Start	12109572:12109572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766265540
CDS Mutation	c.428C>T
AA Mutation	p.Ala143Val(p.A143V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263932
Start	12142411:12142411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1668T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263932
Start	12104508:12104520(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.400_412delGGGATGATTGTCA
AA Mutation	p.Gly134SerfsTer57(p.G134Sfs*57)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263932
Start	12138366:12138367(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1478dupG
AA Mutation	p.Ser495LeufsTer8(p.S495Lfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript