Mutation

Primary Site >> Stomach Cancer

Gene >> TRIM3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6457002:6457002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763067089
CDS Mutation	c.724C>T
AA Mutation	p.Arg242Cys(p.R242C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6456125:6456125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1480G>A
AA Mutation	p.Ala494Thr(p.A494T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6456467:6456467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1259G>A
AA Mutation	p.Arg420His(p.R420H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6457706:6457706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.505G>A
AA Mutation	p.Val169Met(p.V169M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6449174:6449174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778812981
CDS Mutation	c.2089G>A
AA Mutation	p.Asp697Asn(p.D697N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6456810:6456810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.916C>T
AA Mutation	p.Arg306Trp(p.R306W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000345851
Start	6456669:6456669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1057C>T
AA Mutation	p.Arg353Trp(p.R353W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345851
Start	6456511:6456511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766249286
CDS Mutation	c.1215C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345851
Start	6457329:6457329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.663C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345851
Start	6450575:6450575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1917G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000345851
Start	6451396:6451396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1576C>T
AA Mutation	p.Arg526Ter(p.R526*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345851
Start	6451305:6451306(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1666dupT
AA Mutation	p.Trp556LeufsTer8(p.W556Lfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript