Colon Cancer: Gene >> FUT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000391876
Start	48703309:48703309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760999180
CDS Mutation	c.353C>T
AA Mutation	p.Thr118Met(p.T118M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000391876
Start	48703614:48703614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765205410
CDS Mutation	c.658C>T
AA Mutation	p.Arg220Trp(p.R220W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000391876
Start	48703168:48703168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374416675
CDS Mutation	c.212G>A
AA Mutation	p.Arg71His(p.R71H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000391876
Start	48703626:48703626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.670C>A
AA Mutation	p.Gln224Lys(p.Q224K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000391876
Start	48703246:48703246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.290C>A
AA Mutation	p.Ala97Asp(p.A97D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000391876
Start	48703195:48703195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.239C>A
AA Mutation	p.Ala80Asp(p.A80D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000391876
Start	48703818:48703818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.862A>G
AA Mutation	p.Ile288Val(p.I288V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000391876
Start	48703820:48703820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.864T>G
AA Mutation	p.Ile288Met(p.I288M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000391876
Start	48703434:48703434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.478C>A
AA Mutation	p.Leu160Ile(p.L160I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391876
Start	48703826:48703826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535760048
CDS Mutation	c.870G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391876
Start	48703856:48703856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377331559
CDS Mutation	c.900C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391876
Start	48703872:48703872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.916C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391876
Start	48703151:48703151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770562907
CDS Mutation	c.195G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FUT2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391876
Start	48703379:48703379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150802597
CDS Mutation	c.423G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000391876
Start	48703598:48703598(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.646delG
AA Mutation	p.Val216TrpfsTer71(p.V216Wfs*71)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript