Colon Cancer: Gene >> EPN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268933
Start	50536765:50536765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.209A>T
AA Mutation	p.Asn70Ile(p.N70I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268933
Start	50541260:50541260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1281A>C
AA Mutation	p.Lys427Asn(p.K427N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000268933
Start	50536599:50536599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.43C>T
AA Mutation	p.His15Tyr(p.H15Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000268933
Start	50536929:50536929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141972412
CDS Mutation	c.373G>A
AA Mutation	p.Glu125Lys(p.E125K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000268933
Start	50541306:50541306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1327C>T
AA Mutation	p.Pro443Ser(p.P443S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000268933
Start	50541485:50541485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1376C>A
AA Mutation	p.Pro459His(p.P459H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000268933
Start	50536758:50536758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564194484
CDS Mutation	c.202G>A
AA Mutation	p.Gly68Ser(p.G68S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268933
Start	50536685:50536685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754223433
CDS Mutation	c.129C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> EPN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268933
Start	50536596:50536596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370636443
CDS Mutation	c.40G>A
AA Mutation	p.Val14Met(p.V14M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268933
Start	50536877:50536877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.321G>A
Mutation Classification	Silent
Feature Type	Transcript