Colon Cancer: Gene >> PPM1H

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000228705
Start	62832203:62832203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.322G>A
AA Mutation	p.Gly108Arg(p.G108R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000228705
Start	62648604:62648604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540042623
CDS Mutation	c.1430G>A
AA Mutation	p.Arg477His(p.R477H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000228705
Start	62667181:62667181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1394A>G
AA Mutation	p.His465Arg(p.H465R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000228705
Start	62737572:62737572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.884G>T
AA Mutation	p.Arg295Ile(p.R295I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000228705
Start	62648572:62648572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752870905
CDS Mutation	c.1462C>T
AA Mutation	p.Arg488Trp(p.R488W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228705
Start	62801972:62801972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.600C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228705
Start	62802128:62802128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.444G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228705
Start	62648572:62648572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1462C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000228705
Start	62801894:62801894(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.678delC
AA Mutation	p.Thr227HisfsTer30(p.T227Hfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000228705
Start	62788262:62788262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.833T>A
AA Mutation	p.Leu278Ter(p.L278*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PPM1H

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000228705
Start	62832245:62832245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280G>T
AA Mutation	p.Asp94Tyr(p.D94Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript