Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> E2F3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000346618
Start	20482913:20482913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.877A>T
AA Mutation	p.Asn293Tyr(p.N293Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000346618
Start	20481242:20481242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138776759
CDS Mutation	c.542C>T
AA Mutation	p.Thr181Met(p.T181M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000346618
Start	20402237:20402237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5G>T
AA Mutation	p.Arg2Ile(p.R2I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346618
Start	20402259:20402259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.27G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346618
Start	20402319:20402319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.87T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346618
Start	20490295:20490295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773205736
CDS Mutation	c.1263G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346618
Start	20481224:20481224(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.529delA
AA Mutation	p.Thr177ArgfsTer18(p.T177Rfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346618
Start	20481223:20481224(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.529dupA
AA Mutation	p.Thr177AsnfsTer4(p.T177Nfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> E2F3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000346618
Start	20481362:20481362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.662T>C
AA Mutation	p.Ile221Thr(p.I221T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346618
Start	20490376:20490376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779389567
CDS Mutation	c.1344C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346618
Start	20490295:20490295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773205736
CDS Mutation	c.1263G>A
Mutation Classification	Silent
Feature Type	Transcript