Colon Cancer: Gene >> ENO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000234590
Start	8861379:8861379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1286G>A
AA Mutation	p.Arg429Lys(p.R429K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000234590
Start	8867235:8867235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.326A>G
AA Mutation	p.Asn109Ser(p.N109S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000234590
Start	8863988:8863988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.970A>G
AA Mutation	p.Asn324Asp(p.N324D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000234590
Start	8874863:8874863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745490999
CDS Mutation	c.46G>A
AA Mutation	p.Gly16Arg(p.G16R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000234590
Start	8866335:8866335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.611C>T
AA Mutation	p.Ala204Val(p.A204V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000234590
Start	8870469:8870469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.223C>G
AA Mutation	p.Pro75Ala(p.P75A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234590
Start	8867174:8867174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.387C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234590
Start	8867198:8867198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.363T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234590
Start	8868013:8868013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.285C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000234590
Start	8864006:8864006(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.952delG
AA Mutation	p.Asp318MetfsTer5(p.D318Mfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ENO1

No Mutation Annotation!