Colon Cancer: Gene >> PIPOX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323372
Start	29055209:29055209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.954C>A
AA Mutation	p.Ser318Arg(p.S318R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323372
Start	29054560:29054560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.676G>A
AA Mutation	p.Val226Met(p.V226M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000323372
Start	29053559:29053559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.624G>T
AA Mutation	p.Gln208His(p.Q208H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000323372
Start	29054673:29054673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.789G>C
AA Mutation	p.Glu263Asp(p.E263D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000323372
Start	29043245:29043245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.20T>C
AA Mutation	p.Leu7Pro(p.L7P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000323372
Start	29044911:29044911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763783220
CDS Mutation	c.167G>A
AA Mutation	p.Arg56Gln(p.R56Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000323372
Start	29055858:29055858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1012G>T
AA Mutation	p.Asp338Tyr(p.D338Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000323372
Start	29056193:29056193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1061C>T
AA Mutation	p.Ala354Val(p.A354V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323372
Start	29053478:29053478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.543G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000323372
Start	29044877:29044877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148923684
CDS Mutation	c.133C>T
AA Mutation	p.Arg45Ter(p.R45*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PIPOX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323372
Start	29053489:29053489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777572438
CDS Mutation	c.554C>T
AA Mutation	p.Thr185Met(p.T185M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript