Colon Cancer: Gene >> C9orf50

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372478
Start	129613586:129613586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535635348
CDS Mutation	c.892G>A
AA Mutation	p.Val298Ile(p.V298I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372478
Start	129613551:129613551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764011501
CDS Mutation	c.927G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372478
Start	129619817:129619817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772931990
CDS Mutation	c.522G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372478
Start	129619594:129619594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.642G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372478
Start	129619624:129619624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745405190
CDS Mutation	c.612G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000372478
Start	129615544:129615544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199839916
CDS Mutation	c.820C>T
AA Mutation	p.Arg274Ter(p.R274*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> C9orf50

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372478
Start	129613587:129613587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.891C>T
Mutation Classification	Silent
Feature Type	Transcript