Colon Cancer: Gene >> E2F5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000416274
Start	85177651:85177651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.231A>T
AA Mutation	p.Lys77Asn(p.K77N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000416274
Start	85209161:85209161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.635A>C
AA Mutation	p.Lys212Thr(p.K212T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000416274
Start	85212179:85212179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.906C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000416274
Start	85203238:85203238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115346994
CDS Mutation	c.489C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000416274
Start	85203175:85203175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.426G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000416274
Start	85202226:85202226(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs761281897
CDS Mutation	c.320delA
AA Mutation	p.Lys107SerfsTer11(p.K107Sfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000416274
Start	85209379:85209379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.853C>T
AA Mutation	p.Gln285Ter(p.Q285*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> E2F5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000416274
Start	85203249:85203249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.500A>T
AA Mutation	p.Asn167Ile(p.N167I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000416274
Start	85206196:85206196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.526G>T
AA Mutation	p.Glu176Ter(p.E176*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript