Colon Cancer: Gene >> UNG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242576
Start	109098595:109098595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.296A>T
AA Mutation	p.Lys99Met(p.K99M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000242576
Start	109109832:109109832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143034537
CDS Mutation	c.805C>T
AA Mutation	p.Arg269Trp(p.R269W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000242576
Start	109103450:109103450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.640G>A
AA Mutation	p.Ala214Thr(p.A214T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000242576
Start	109097725:109097725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.46G>A
AA Mutation	p.Ala16Thr(p.A16T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242576
Start	109101937:109101937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780271583
CDS Mutation	c.471T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained;protein_altering_variant
Transcription ID	ENST00000242576
Start	109103495:109103496(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.685_686insTAAATCCAT
AA Mutation	p.Arg229delinsLeuAsnProTer(p.R229delinsLNP*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000242576
Start	109098608:109098609(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.313dupG
AA Mutation	p.Glu105GlyfsTer38(p.E105Gfs*38)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> UNG

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242576
Start	109103548:109103548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs187858476
CDS Mutation	c.738G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242576
Start	109098599:109098599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773617744
CDS Mutation	c.300G>A
Mutation Classification	Silent
Feature Type	Transcript