Colon Cancer: Gene >> PPP1CC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335007
Start	110721146:110721146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.902A>C
AA Mutation	p.Lys301Thr(p.K301T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335007
Start	110742680:110742680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.28G>A
AA Mutation	p.Asp10Asn(p.D10N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335007
Start	110730639:110730639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.308C>T
AA Mutation	p.Thr103Met(p.T103M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335007
Start	110730599:110730599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.348G>T
AA Mutation	p.Glu116Asp(p.E116D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PPP1CC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335007
Start	110722609:110722609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.610C>A
AA Mutation	p.Leu204Ile(p.L204I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335007
Start	110730713:110730713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767247849
CDS Mutation	c.234C>T
Mutation Classification	Silent
Feature Type	Transcript