Colon Cancer: Gene >> EDN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337938
Start	59301622:59301622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265C>A
AA Mutation	p.Pro89Thr(p.P89T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337938
Start	59321129:59321129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778461734
CDS Mutation	c.478G>A
AA Mutation	p.Ala160Thr(p.A160T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337938
Start	59301520:59301520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774307682
CDS Mutation	c.163G>A
AA Mutation	p.Glu55Lys(p.E55K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000337938
Start	59301643:59301643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.286C>T
AA Mutation	p.Arg96Cys(p.R96C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000337938
Start	59322383:59322383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368327225
CDS Mutation	c.554C>T
AA Mutation	p.Thr185Met(p.T185M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000337938
Start	59301452:59301452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.95G>T
AA Mutation	p.Gly32Val(p.G32V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337938
Start	59324369:59324369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.627C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337938
Start	59321165:59321165(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.517delT
AA Mutation	p.Cys173AlafsTer36(p.C173Afs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> EDN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337938
Start	59322375:59322375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.546T>G
AA Mutation	p.Asn182Lys(p.N182K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337938
Start	59324345:59324345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758459588
CDS Mutation	c.603C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337938
Start	59301561:59301561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.204G>A
Mutation Classification	Silent
Feature Type	Transcript