Colon Cancer: Gene >> PPOX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000352210
Start	161169064:161169064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.688C>T
AA Mutation	p.Arg230Cys(p.R230C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000352210
Start	161167433:161167433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.285G>T
AA Mutation	p.Gln95His(p.Q95H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000352210
Start	161170475:161170475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1054G>C
AA Mutation	p.Ala352Pro(p.A352P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000352210
Start	161169690:161169690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.838G>C
AA Mutation	p.Asp280His(p.D280H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000352210
Start	161171132:161171132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147480828
CDS Mutation	c.1390C>T
AA Mutation	p.Arg464Cys(p.R464C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352210
Start	161167183:161167183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.171A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352210
Start	161170009:161170009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.972C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352210
Start	161167196:161167196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.184A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000352210
Start	161168534:161168535(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.577dupA
AA Mutation	p.Thr193AsnfsTer30(p.T193Nfs*30)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PPOX

No Mutation Annotation!