Colon Cancer: Gene >> MPG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000219431
Start	85640:85640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.760C>T
AA Mutation	p.Pro254Ser(p.P254S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000219431
Start	79563:79563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61753368
CDS Mutation	c.178C>T
AA Mutation	p.Arg60Cys(p.R60C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000219431
Start	79684:79684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.299G>A
AA Mutation	p.Arg100Gln(p.R100Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000219431
Start	85616:85616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.736C>T
AA Mutation	p.Arg246Cys(p.R246C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000219431
Start	85520:85520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.640C>T
AA Mutation	p.Leu214Phe(p.L214F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219431
Start	85405:85405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751887856
CDS Mutation	c.525C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000219431
Start	79300:79300(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.12delC
AA Mutation	p.Ala5LeufsTer4(p.A5Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MPG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000219431
Start	83134:83134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.398A>C
AA Mutation	p.Glu133Ala(p.E133A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript