Colon Cancer: Gene >> NUBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000283027
Start	10761787:10761787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.748G>A
AA Mutation	p.Gly250Arg(p.G250R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000283027
Start	10757913:10757913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.492G>T
AA Mutation	p.Glu164Asp(p.E164D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283027
Start	10757973:10757973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.552C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000283027
Start	10761391:10761391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.634G>T
AA Mutation	p.Glu212Ter(p.E212*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000283027
Start	10744023:10744023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.82C>T
AA Mutation	p.Gln28Ter(p.Q28*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000283027
Start	10757914:10757915(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.493_494insAATCCACAGGGGATGCTTACTTT
AA Mutation	p.Val165GlufsTer40(p.V165Efs*40)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NUBP1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283027
Start	10747234:10747234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148295916
CDS Mutation	c.216C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000283027
Start	10761391:10761391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.634G>T
AA Mutation	p.Glu212Ter(p.E212*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript