Colon Cancer: Gene >> PPM1G

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344034
Start	27384009:27384009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.909G>T
AA Mutation	p.Glu303Asp(p.E303D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344034
Start	27384751:27384751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.747T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344034
Start	27386263:27386263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138207162
CDS Mutation	c.207G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000344034
Start	27383389:27383389(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1178delG
AA Mutation	p.Gly393AlafsTer25(p.G393Afs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000344034
Start	27383508:27383508(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1059delA
AA Mutation	p.Ser354LeufsTer7(p.S354Lfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PPM1G

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344034
Start	27381628:27381628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770886509
CDS Mutation	c.1612G>A
AA Mutation	p.Asp538Asn(p.D538N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344034
Start	27384730:27384730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.768C>A
AA Mutation	p.Phe256Leu(p.F256L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript