Colon Cancer: Gene >> PPM1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395076
Start	60282800:60282800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.97C>T
AA Mutation	p.Arg33Cys(p.R33C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000395076
Start	60289838:60289838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756924885
CDS Mutation	c.985G>A
AA Mutation	p.Asp329Asn(p.D329N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000395076
Start	60283127:60283127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.424A>G
AA Mutation	p.Ile142Val(p.I142V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000395076
Start	60282801:60282801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.98G>A
AA Mutation	p.Arg33His(p.R33H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000395076
Start	60282729:60282729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.26A>C
AA Mutation	p.Lys9Thr(p.K9T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000395076
Start	60283046:60283046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.343A>G
AA Mutation	p.Met115Val(p.M115V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000395076
Start	60289857:60289857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755451132
CDS Mutation	c.1004G>A
AA Mutation	p.Arg335His(p.R335H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PPM1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395076
Start	60292471:60292471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1138G>A
AA Mutation	p.Asp380Asn(p.D380N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000395076
Start	60289832:60289832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746894375
CDS Mutation	c.979G>A
AA Mutation	p.Val327Ile(p.V327I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395076
Start	60282859:60282859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149289409
CDS Mutation	c.156G>A
Mutation Classification	Silent
Feature Type	Transcript