Colon Cancer: Gene >> PPP2R1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000527614
Start	111747983:111747983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1370C>T
AA Mutation	p.Ser457Phe(p.S457F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000527614
Start	111743463:111743463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1467G>T
AA Mutation	p.Trp489Cys(p.W489C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000527614
Start	111752207:111752207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1290G>T
AA Mutation	p.Arg430Ser(p.R430S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000527614
Start	111755329:111755329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781839059
CDS Mutation	c.809G>A
AA Mutation	p.Arg270His(p.R270H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000527614
Start	111754516:111754516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1012A>T
AA Mutation	p.Ile338Phe(p.I338F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000527614
Start	111742107:111742107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1735T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PPP2R1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000527614
Start	111748007:111748007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1346A>C
AA Mutation	p.Glu449Ala(p.E449A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000527614
Start	111748003:111748003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1350C>A
AA Mutation	p.Phe450Leu(p.F450L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript