Colon Cancer: Gene >> PCK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216780
Start	24103935:24103935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1894G>A
AA Mutation	p.Ala632Thr(p.A632T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216780
Start	24103523:24103523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1482G>A
AA Mutation	p.Met494Ile(p.M494I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216780
Start	24099594:24099594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.889T>A
AA Mutation	p.Tyr297Asn(p.Y297N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216780
Start	24098238:24098238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765912476
CDS Mutation	c.311G>A
AA Mutation	p.Arg104Gln(p.R104Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000216780
Start	24103647:24103647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763930692
CDS Mutation	c.1606C>T
AA Mutation	p.Arg536Trp(p.R536W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216780
Start	24103730:24103730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1689G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PCK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216780
Start	24102858:24102858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1340A>G
AA Mutation	p.Asp447Gly(p.D447G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216780
Start	24098579:24098579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377444905
CDS Mutation	c.565C>T
AA Mutation	p.Arg189Cys(p.R189C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript