Colon Cancer: Gene >> FUT5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252675
Start	5867671:5867671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755351741
CDS Mutation	c.55G>A
AA Mutation	p.Gly19Arg(p.G19R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000252675
Start	5867065:5867065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781634935
CDS Mutation	c.661C>T
AA Mutation	p.Arg221Cys(p.R221C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000252675
Start	5867100:5867100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374990298
CDS Mutation	c.626C>T
AA Mutation	p.Ala209Val(p.A209V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000252675
Start	5867374:5867374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752890602
CDS Mutation	c.352G>A
AA Mutation	p.Ala118Thr(p.A118T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000252675
Start	5866746:5866746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.980C>G
AA Mutation	p.Ala327Gly(p.A327G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FUT5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252675
Start	5866758:5866758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768406993
CDS Mutation	c.968A>G
AA Mutation	p.Asp323Gly(p.D323G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript