Colon Cancer: Gene >> E2F4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379378
Start	67192286:67192286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.59A>C
AA Mutation	p.Lys20Thr(p.K20T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379378
Start	67195922:67195922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.949A>G
AA Mutation	p.Ser317Gly(p.S317G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379378
Start	67194820:67194820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.648C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379378
Start	67193126:67193126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.363G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000379378
Start	67195891:67195893(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs774472392
CDS Mutation	c.956_958delGCA
AA Mutation	p.Ser319del(p.S319del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> E2F4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379378
Start	67192808:67192808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.183T>G
AA Mutation	p.Ile61Met(p.I61M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript