Colon Cancer: Gene >> PPP4C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000279387
Start	30084988:30084988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.850A>G
AA Mutation	p.Ile284Val(p.I284V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000279387
Start	30084767:30084767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.706C>A
AA Mutation	p.Arg236Ser(p.R236S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000279387
Start	30083455:30083455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.365A>G
AA Mutation	p.Gln122Arg(p.Q122R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000279387
Start	30083755:30083755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.578G>A
AA Mutation	p.Cys193Tyr(p.C193Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000279387
Start	30083669:30083669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373650531
CDS Mutation	c.492C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000279387
Start	30082814:30082814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373393404
CDS Mutation	c.270C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000279387
Start	30085020:30085020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.882G>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PPP4C

No Mutation Annotation!