Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TRA2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000453386
Start	185921144:185921144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.682C>T
AA Mutation	p.Arg228Trp(p.R228W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000453386
Start	185922089:185922089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.560G>A
AA Mutation	p.Arg187His(p.R187H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000453386
Start	185923936:185923936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.382T>C
AA Mutation	p.Tyr128His(p.Y128H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000453386
Start	185925465:185925465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.332G>T
AA Mutation	p.Arg111Leu(p.R111L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000453386
Start	185925581:185925581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.216G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000453386
Start	185925604:185925604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.193C>T
AA Mutation	p.Arg65Ter(p.R65*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000453386
Start	185919471:185919472(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs779996960
CDS Mutation	c.745_747dupGGA
AA Mutation	p.Gly249dup(p.G249dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TRA2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000453386
Start	185925534:185925534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.263G>A
AA Mutation	p.Arg88Gln(p.R88Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000453386
Start	185922090:185922090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.559C>T
AA Mutation	p.Arg187Cys(p.R187C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000453386
Start	185925603:185925603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777354455
CDS Mutation	c.194G>A
AA Mutation	p.Arg65Gln(p.R65Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000453386
Start	185922033:185922033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.616A>C
AA Mutation	p.Ile206Leu(p.I206L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript