Colon Cancer: Gene >> PDP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297598
Start	93922871:93922871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.812G>T
AA Mutation	p.Gly271Val(p.G271V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297598
Start	93923397:93923397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1338A>G
AA Mutation	p.Ile446Met(p.I446M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000297598
Start	93923509:93923509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745958515
CDS Mutation	c.1450C>T
AA Mutation	p.Arg484Cys(p.R484C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000297598
Start	93922443:93922443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.384T>A
AA Mutation	p.Ser128Arg(p.S128R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000297598
Start	93923003:93923003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.944A>C
AA Mutation	p.Asn315Thr(p.N315T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297598
Start	93923022:93923022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.963A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297598
Start	93922953:93922953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.894G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297598
Start	93922536:93922536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.477C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297598
Start	93922356:93922356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.297A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000297598
Start	93922816:93922817(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.758_759dupTT
AA Mutation	p.Gly254LeufsTer70(p.G254Lfs*70)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PDP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297598
Start	93922584:93922584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.525G>T
AA Mutation	p.Glu175Asp(p.E175D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297598
Start	93923020:93923020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.961G>A
AA Mutation	p.Glu321Lys(p.E321K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000297598
Start	93923594:93923594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1535G>A
AA Mutation	p.Arg512Gln(p.R512Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000297598
Start	93922855:93922855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.796C>T
AA Mutation	p.Arg266Ter(p.R266*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000297598
Start	93923020:93923020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.961G>T
AA Mutation	p.Glu321Ter(p.E321*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript