Colon Cancer: Gene >> PPP1CB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296122
Start	28776958:28776958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160T>G
AA Mutation	p.Leu54Val(p.L54V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296122
Start	28776869:28776869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.71G>A
AA Mutation	p.Gly24Glu(p.G24E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296122
Start	28776892:28776892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760562458
CDS Mutation	c.94G>A
AA Mutation	p.Ala32Thr(p.A32T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296122
Start	28778942:28778942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.318A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296122
Start	28788708:28788709(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.647dupG
AA Mutation	p.Glu217ArgfsTer3(p.E217Rfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PPP1CB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296122
Start	28776955:28776955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.157G>A
AA Mutation	p.Glu53Lys(p.E53K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296122
Start	28788668:28788668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.603T>C
Mutation Classification	Silent
Feature Type	Transcript