Colon Cancer: Gene >> PPM1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000498165
Start	160756591:160756591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283G>A
AA Mutation	p.Val95Met(p.V95M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000498165
Start	161068841:161068841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.767G>T
AA Mutation	p.Arg256Met(p.R256M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000498165
Start	161069054:161069054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.980G>T
AA Mutation	p.Gly327Val(p.G327V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000498165
Start	161065498:161065498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757453078
CDS Mutation	c.670G>A
AA Mutation	p.Ala224Thr(p.A224T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000498165
Start	161068962:161068962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.888C>A
AA Mutation	p.Phe296Leu(p.F296L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000498165
Start	161068865:161068865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.791C>A
AA Mutation	p.Ser264Tyr(p.S264Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000498165
Start	160961805:160961805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469G>T
AA Mutation	p.Asp157Tyr(p.D157Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000498165
Start	160756652:160756652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.344T>C
AA Mutation	p.Leu115Pro(p.L115P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000498165
Start	161069030:161069030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.956A>C
AA Mutation	p.Glu319Ala(p.E319A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000498165
Start	161065497:161065497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754388001
CDS Mutation	c.669C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000498165
Start	161069017:161069017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.943C>T
AA Mutation	p.Arg315Ter(p.R315*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PPM1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000498165
Start	160756399:160756399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.91A>T
AA Mutation	p.Ile31Phe(p.I31F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000498165
Start	161069119:161069119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1045G>T
AA Mutation	p.Val349Leu(p.V349L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000498165
Start	160961798:160961798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755440707
CDS Mutation	c.462C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000498165
Start	160961811:160961811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.475G>T
AA Mutation	p.Glu159Ter(p.E159*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript