Colon Cancer: Gene >> PPP1CA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376745
Start	67400699:67400699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.408C>A
AA Mutation	p.Phe136Leu(p.F136L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376745
Start	67398789:67398789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.815A>G
AA Mutation	p.Tyr272Cys(p.Y272C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376745
Start	67399656:67399656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.428G>A
AA Mutation	p.Arg143His(p.R143H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376745
Start	67398725:67398725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.879C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376745
Start	67398613:67398613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.915G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant;splice_donor_variant;intron_variant
Transcription ID	ENST00000376745
Start	67398646:67398721(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.883-1_882+1delGTGAGTGTGGGGAAGAAAGGAGCCGCTAGGCCCTGTGGCTCAGCCCCATGAGCCTGACCAACACTGTCTCTTTTAG
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PPP1CA

No Mutation Annotation!