Colon Cancer: Gene >> ENO3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323997
Start	4955509:4955509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.770A>G
AA Mutation	p.Tyr257Cys(p.Y257C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323997
Start	4956106:4956106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755474025
CDS Mutation	c.1030G>A
AA Mutation	p.Val344Ile(p.V344I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000323997
Start	4955151:4955151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.521G>T
AA Mutation	p.Gly174Val(p.G174V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000323997
Start	4955232:4955232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.602G>T
AA Mutation	p.Gly201Val(p.G201V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000323997
Start	4953778:4953778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.377A>G
AA Mutation	p.Lys126Arg(p.K126R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323997
Start	4955092:4955092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.462C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323997
Start	4956842:4956842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753649833
CDS Mutation	c.1188C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000323997
Start	4956599:4956599(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1099delG
AA Mutation	p.Val367Ter(p.V367*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000323997
Start	4956844:4956844(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1194delC
AA Mutation	p.Cys399AlafsTer13(p.C399Afs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ENO3

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323997
Start	4956135:4956135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768457126
CDS Mutation	c.1059G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000323997
Start	4952842:4952842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.133G>T
AA Mutation	p.Glu45Ter(p.E45*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript