Colon Cancer: Gene >> SEPT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360051
Start	241336043:241336043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.286C>T
AA Mutation	p.Arg96Cys(p.R96C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360051
Start	241336079:241336079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.322G>A
AA Mutation	p.Ala108Thr(p.A108T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000360051
Start	241337790:241337790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.594G>T
AA Mutation	p.Arg198Ser(p.R198S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360051
Start	241343761:241343761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.706C>T
AA Mutation	p.Pro236Ser(p.P236S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360051
Start	241346222:241346222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191642496
CDS Mutation	c.899G>A
AA Mutation	p.Arg300His(p.R300H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360051
Start	241343051:241343051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.654A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SEPT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360051
Start	241343777:241343777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.722G>C
AA Mutation	p.Gly241Ala(p.G241A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360051
Start	241337457:241337457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.417G>A
Mutation Classification	Silent
Feature Type	Transcript