Colon Cancer: Gene >> NAPSA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253719
Start	50361698:50361698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186910155
CDS Mutation	c.433C>T
AA Mutation	p.Arg145Trp(p.R145W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253719
Start	50358725:50358725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1091C>A
AA Mutation	p.Pro364His(p.P364H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000253719
Start	50359019:50359019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1027G>A
AA Mutation	p.Val343Ile(p.V343I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000253719
Start	50362303:50362303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.94C>A
AA Mutation	p.His32Asn(p.H32N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253719
Start	50365610:50365610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750561281
CDS Mutation	c.12A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253719
Start	50359856:50359856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.675T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253719
Start	50358625:50358625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1191C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000253719
Start	50359649:50359649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.792-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> NAPSA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253719
Start	50362031:50362031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.287A>G
AA Mutation	p.Asp96Gly(p.D96G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253719
Start	50362073:50362073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.245T>C
AA Mutation	p.Ile82Thr(p.I82T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253719
Start	50362199:50362199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199668068
CDS Mutation	c.198C>A
Mutation Classification	Silent
Feature Type	Transcript