Mutation

Primary Site >> Stomach Cancer

Gene >> TRAF3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392745
Start	102905237:102905237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1160G>A
AA Mutation	p.Arg387Gln(p.R387Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392745
Start	102875679:102875679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749373923
CDS Mutation	c.353G>A
AA Mutation	p.Arg118Gln(p.R118Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392745
Start	102875654:102875654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.328A>C
AA Mutation	p.Ile110Leu(p.I110L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392745
Start	102876443:102876443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774090745
CDS Mutation	c.488G>A
AA Mutation	p.Arg163Gln(p.R163Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000392745
Start	102876461:102876461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.506C>T
AA Mutation	p.Ala169Val(p.A169V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000392745
Start	102905776:102905776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1699G>A
AA Mutation	p.Asp567Asn(p.D567N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000392745
Start	102905661:102905661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1584G>A
AA Mutation	p.Met528Ile(p.M528I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392745
Start	102905760:102905760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1683T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392745
Start	102871941:102871941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149018928
CDS Mutation	c.270G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392745
Start	102905336:102905336(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1260delG
AA Mutation	p.Trp420Ter(p.W420*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392745
Start	102905700:102905701(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1624_1625delGT
AA Mutation	p.Val542SerfsTer8(p.V542Sfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000392745
Start	102905590:102905590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1513C>T
AA Mutation	p.Arg505Ter(p.R505*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript