Colon Cancer: Gene >> CTPS2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000359276
Start	16698923:16698923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.337G>T
AA Mutation	p.Val113Phe(p.V113F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359276
Start	16702883:16702883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200869248
CDS Mutation	c.20C>T
AA Mutation	p.Thr7Met(p.T7M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359276
Start	16689504:16689504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.818C>T
AA Mutation	p.Pro273Leu(p.P273L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359276
Start	16689474:16689474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.848T>A
AA Mutation	p.Phe283Tyr(p.F283Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359276
Start	16639176:16639176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1364C>A
AA Mutation	p.Thr455Asn(p.T455N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359276
Start	16683195:16683195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.904G>A
AA Mutation	p.Ala302Thr(p.A302T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359276
Start	16609569:16609569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1663T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359276
Start	16617235:16617236(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1460_1461insT
AA Mutation	p.Leu488ProfsTer6(p.L488Pfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000359276
Start	16617247:16617247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1450-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000359276
Start	16693460:16693461(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.465_466insTACTTATCT
AA Mutation	p.Glu155_Gly156insTyrLeuSer(p.E155_G156insYLS)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CTPS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359276
Start	16683112:16683112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.987C>A
AA Mutation	p.Asn329Lys(p.N329K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359276
Start	16693407:16693407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.519G>T
AA Mutation	p.Glu173Asp(p.E173D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359276
Start	16689484:16689484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.838A>G
AA Mutation	p.Asn280Asp(p.N280D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript