Colon Cancer: Gene >> FUT8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360689
Start	65561685:65561685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771685724
CDS Mutation	c.122G>A
AA Mutation	p.Arg41Gln(p.R41Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360689
Start	65616226:65616226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.335A>G
AA Mutation	p.His112Arg(p.H112R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360689
Start	65733293:65733293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758856033
CDS Mutation	c.1322G>A
AA Mutation	p.Arg441Gln(p.R441Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360689
Start	65669383:65669383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.738G>T
AA Mutation	p.Gln246His(p.Q246H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360689
Start	65742361:65742361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1679A>G
AA Mutation	p.Glu560Gly(p.E560G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000360689
Start	65742357:65742357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769250336
CDS Mutation	c.1675C>T
AA Mutation	p.Arg559Ter(p.R559*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000360689
Start	65721920:65721920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.981G>A
AA Mutation	p.Trp327Ter(p.W327*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360689
Start	65616077:65616078(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.303_304insCTCACTTTCT
AA Mutation	p.Lys102LeufsTer4(p.K102Lfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FUT8

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360689
Start	65669296:65669296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.651C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000360689
Start	65721972:65721972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1033G>T
AA Mutation	p.Glu345Ter(p.E345*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000360689
Start	65742357:65742357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769250336
CDS Mutation	c.1675C>T
AA Mutation	p.Arg559Ter(p.R559*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000360689
Start	65742099:65742099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1417C>T
AA Mutation	p.Arg473Ter(p.R473*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript