Colon Cancer: Gene >> ENOSF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000251101
Start	674331:674331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1306A>G
AA Mutation	p.Lys436Glu(p.K436E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000251101
Start	706529:706529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134C>T
AA Mutation	p.Ala45Val(p.A45V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000251101
Start	683295:683295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.827A>G
AA Mutation	p.Glu276Gly(p.E276G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000251101
Start	694283:694283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361G>A
AA Mutation	p.Ala121Thr(p.A121T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251101
Start	706546:706546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139918997
CDS Mutation	c.117C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251101
Start	677771:677771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1020A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251101
Start	706501:706501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.162T>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ENOSF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000251101
Start	685927:685927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.735G>T
AA Mutation	p.Lys245Asn(p.K245N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000251101
Start	706551:706551(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.112delT
AA Mutation	p.Tyr38MetfsTer4(p.Y38Mfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript