Colon Cancer: Gene >> FAR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354817
Start	13714634:13714634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1081G>A
AA Mutation	p.Ala361Thr(p.A361T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354817
Start	13712019:13712019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753671320
CDS Mutation	c.860C>T
AA Mutation	p.Ala287Val(p.A287V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354817
Start	13700369:13700369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.242C>T
AA Mutation	p.Ala81Val(p.A81V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354817
Start	13707950:13707950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.416C>T
AA Mutation	p.Ala139Val(p.A139V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000354817
Start	13727574:13727574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1276C>T
AA Mutation	p.Arg426Trp(p.R426W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000354817
Start	13707978:13707978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.444C>A
AA Mutation	p.Phe148Leu(p.F148L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354817
Start	13727591:13727591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150400003
CDS Mutation	c.1293A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354817
Start	13711778:13711778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.738C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354817
Start	13714546:13714546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.993C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FAR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354817
Start	13694799:13694799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.34A>C
AA Mutation	p.Asn12His(p.N12H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354817
Start	13700360:13700360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.233A>T
AA Mutation	p.Lys78Ile(p.K78I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript