Colon Cancer: Gene >> TYMS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323274
Start	670835:670835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.700A>G
AA Mutation	p.Thr234Ala(p.T234A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323274
Start	670822:670822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.687C>G
AA Mutation	p.Ser229Arg(p.S229R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000323274
Start	657939:657939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.197G>A
AA Mutation	p.Ser66Asn(p.S66N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323274
Start	669136:669136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770269195
CDS Mutation	c.519C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323274
Start	670771:670771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.636G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323274
Start	670769:670769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.634C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000323274
Start	669102:669103(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.486_487delAA
AA Mutation	p.Arg163SerfsTer3(p.R163Sfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TYMS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323274
Start	669144:669144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.527G>A
AA Mutation	p.Arg176Lys(p.R176K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000323274
Start	672902:672902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.847C>T
AA Mutation	p.Arg283Ter(p.R283*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript