Colon Cancer: Gene >> SLC35A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370155
Start	100007041:100007041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.350A>T
AA Mutation	p.Tyr117Phe(p.Y117F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370155
Start	100011520:100011520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.621A>C
AA Mutation	p.Arg207Ser(p.R207S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370155
Start	99999410:99999410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.337T>A
AA Mutation	p.Tyr113Asn(p.Y113N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370155
Start	99999318:99999318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.245T>C
AA Mutation	p.Met82Thr(p.M82T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370155
Start	100015397:100015397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.730A>G
AA Mutation	p.Thr244Ala(p.T244A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370155
Start	100022401:100022401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.903A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000370155
Start	100015352:100015352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.685G>T
AA Mutation	p.Glu229Ter(p.E229*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC35A3

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370155
Start	100017759:100017759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749734512
CDS Mutation	c.831G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370155
Start	100017786:100017786(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.862delT
AA Mutation	p.Trp288GlyfsTer18(p.W288Gfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript