Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SRR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344595
Start	2317891:2317891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761174722
CDS Mutation	c.190G>A
AA Mutation	p.Val64Ile(p.V64I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344595
Start	2321313:2321313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.407A>T
AA Mutation	p.Glu136Val(p.E136V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344595
Start	2315679:2315679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766468296
CDS Mutation	c.119G>A
AA Mutation	p.Arg40His(p.R40H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000344595
Start	2318875:2318875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.345A>C
AA Mutation	p.Lys115Asn(p.K115N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344595
Start	2321335:2321335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.429A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000344595
Start	2321581:2321581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.559G>T
AA Mutation	p.Gly187Ter(p.G187*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SRR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344595
Start	2323842:2323842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.992G>T
AA Mutation	p.Arg331Met(p.R331M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344595
Start	2315568:2315568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748628404
CDS Mutation	c.8C>T
AA Mutation	p.Ala3Val(p.A3V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000344595
Start	2321312:2321312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.406G>T
AA Mutation	p.Glu136Ter(p.E136*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript