Colon Cancer: Gene >> DCN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000052754
Start	91151690:91151690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.849A>C
AA Mutation	p.Arg283Ser(p.R283S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000052754
Start	91153171:91153171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144174426
CDS Mutation	c.671C>T
AA Mutation	p.Thr224Met(p.T224M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000052754
Start	91158409:91158409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.425A>C
AA Mutation	p.Lys142Thr(p.K142T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000052754
Start	91157164:91157164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.563G>T
AA Mutation	p.Ser188Ile(p.S188I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000052754
Start	91146093:91146093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200191955
CDS Mutation	c.1045G>A
AA Mutation	p.Val349Met(p.V349M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000052754
Start	91158385:91158385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.449A>C
AA Mutation	p.Lys150Thr(p.K150T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000052754
Start	91164646:91164646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283G>A
AA Mutation	p.Glu95Lys(p.E95K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000052754
Start	91157172:91157172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147765043
CDS Mutation	c.555G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000052754
Start	91178366:91178367(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.186dupT
AA Mutation	p.Arg63SerfsTer7(p.R63Sfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000052754
Start	91158391:91158392(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.442dupA
AA Mutation	p.Met148AsnfsTer12(p.M148Nfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DCN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000052754
Start	91164646:91164646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283G>A
AA Mutation	p.Glu95Lys(p.E95K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript