Colon Cancer: Gene >> FUCA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374479
Start	23865525:23865525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.490T>A
AA Mutation	p.Leu164Met(p.L164M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374479
Start	23845849:23845849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1267A>T
AA Mutation	p.Met423Leu(p.M423L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374479
Start	23854458:23854458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.871C>T
AA Mutation	p.His291Tyr(p.H291Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374479
Start	23865511:23865511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.504G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374479
Start	23868068:23868068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.219C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374479
Start	23863241:23863244(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.552_555delACTC
AA Mutation	p.Leu185Ter(p.L185*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FUCA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374479
Start	23854538:23854538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778251523
CDS Mutation	c.791G>A
AA Mutation	p.Arg264Gln(p.R264Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000374479
Start	23854377:23854377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.952G>T
AA Mutation	p.Glu318Ter(p.E318*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript