Colon Cancer: Gene >> NUCB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000529010
Start	17310849:17310849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.508G>T
AA Mutation	p.Asp170Tyr(p.D170Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000529010
Start	17315421:17315421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.948G>T
AA Mutation	p.Glu316Asp(p.E316D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000529010
Start	17330921:17330921(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1200delA
AA Mutation	p.Lys400AsnfsTer15(p.K400Nfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000529010
Start	17311267:17311268(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.749dupT
AA Mutation	p.Lys251GlnfsTer4(p.K251Qfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NUCB2

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000529010
Start	17330169:17330169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1045G>T
AA Mutation	p.Glu349Ter(p.E349*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000529010
Start	17301809:17301810(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.322dupA
AA Mutation	p.Arg108LysfsTer12(p.R108Kfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript