Colon Cancer: Gene >> ENOX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261488
Start	43359925:43359925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757929801
CDS Mutation	c.515G>A
AA Mutation	p.Arg172Gln(p.R172Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261488
Start	43356086:43356086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.656C>A
AA Mutation	p.Ala219Asp(p.A219D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261488
Start	43360001:43360001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.439G>A
AA Mutation	p.Gly147Arg(p.G147R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261488
Start	43356107:43356107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.635G>A
AA Mutation	p.Gly212Asp(p.G212D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261488
Start	43344631:43344631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.943C>T
AA Mutation	p.Arg315Cys(p.R315C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261488
Start	43356014:43356014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779420488
CDS Mutation	c.728G>A
AA Mutation	p.Arg243His(p.R243H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261488
Start	43322394:43322394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1251C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261488
Start	43361295:43361295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.366T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261488
Start	43355944:43355944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374431410
CDS Mutation	c.798C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261488
Start	43359945:43359945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781034473
CDS Mutation	c.495C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261488
Start	43236718:43236718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1632T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261488
Start	43361292:43361292(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.369delT
AA Mutation	p.Pro124LeufsTer79(p.P124Lfs*79)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ENOX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261488
Start	43412891:43412891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.24G>T
AA Mutation	p.Glu8Asp(p.E8D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261488
Start	43344575:43344575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.999G>T
AA Mutation	p.Glu333Asp(p.E333D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261488
Start	43236733:43236733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1617C>A
Mutation Classification	Silent
Feature Type	Transcript