Colon Cancer: Gene >> PDK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000503176
Start	50110093:50110093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1220G>A
AA Mutation	p.Ser407Asn(p.S407N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000503176
Start	50095472:50095472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.37C>A
AA Mutation	p.Leu13Met(p.L13M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000503176
Start	50110087:50110087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1214G>A
AA Mutation	p.Arg405His(p.R405H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000503176
Start	50095513:50095513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.78C>A
AA Mutation	p.Phe26Leu(p.F26L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000503176
Start	50097426:50097426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.122C>T
AA Mutation	p.Ser41Phe(p.S41F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000503176
Start	50108388:50108388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832G>A
AA Mutation	p.Ala278Thr(p.A278T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000503176
Start	50095479:50095479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.44G>A
AA Mutation	p.Gly15Glu(p.G15E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000503176
Start	50109968:50109968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760337566
CDS Mutation	c.1095G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000503176
Start	50108688:50108688(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.943delC
AA Mutation	p.Gln315SerfsTer142(p.Q315Sfs*142)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PDK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000503176
Start	50109395:50109395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1078C>A
AA Mutation	p.Leu360Ile(p.L360I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript