Colon Cancer: Gene >> NOG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332822
Start	56594386:56594386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.163G>A
AA Mutation	p.Asp55Asn(p.D55N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000332822
Start	56594647:56594647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.424C>T
AA Mutation	p.Arg142Trp(p.R142W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332822
Start	56594695:56594695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.472C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332822
Start	56594412:56594412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.189G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332822
Start	56594340:56594340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.117C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NOG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332822
Start	56594717:56594717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.494G>A
AA Mutation	p.Gly165Asp(p.G165D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000332822
Start	56594688:56594688(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.468delC
AA Mutation	p.Val157CysfsTer17(p.V157Cfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript