Colon Cancer: Gene >> PLOD3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000223127
Start	101217259:101217259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.16C>T
AA Mutation	p.Pro6Ser(p.P6S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000223127
Start	101213162:101213162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141948483
CDS Mutation	c.722G>A
AA Mutation	p.Arg241Gln(p.R241Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000223127
Start	101211685:101211685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1264G>A
AA Mutation	p.Gly422Ser(p.G422S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000223127
Start	101216286:101216286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.379A>C
AA Mutation	p.Lys127Gln(p.K127Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000223127
Start	101212922:101212922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.799A>G
AA Mutation	p.Asn267Asp(p.N267D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000223127
Start	101211867:101211867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1211G>T
AA Mutation	p.Arg404Leu(p.R404L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223127
Start	101212917:101212917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202155755
CDS Mutation	c.804C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223127
Start	101215980:101215980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.543C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223127
Start	101215956:101215956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201040631
CDS Mutation	c.567C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223127
Start	101206854:101206854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs117761436
CDS Mutation	c.1986G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223127
Start	101217223:101217223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.52C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223127
Start	101210138:101210138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1638C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000223127
Start	101210092:101210092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1683+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PLOD3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000223127
Start	101208884:101208884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1757A>T
AA Mutation	p.His586Leu(p.H586L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000223127
Start	101215095:101215095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.673G>A
AA Mutation	p.Ala225Thr(p.A225T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript