Colon Cancer: Gene >> SUPV3L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359655
Start	69203021:69203021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1754T>G
AA Mutation	p.Phe585Cys(p.F585C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359655
Start	69185994:69185994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.279A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359655
Start	69189363:69189363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.669A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000359655
Start	69208655:69208655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1981G>T
AA Mutation	p.Glu661Ter(p.E661*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000359655
Start	69198453:69198454(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1105_1106insAGTAATTAAGTGAAAA
AA Mutation	p.Cys369Ter(p.C369*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000359655
Start	69202520:69202520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1599+1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SUPV3L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359655
Start	69202514:69202514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1594C>T
AA Mutation	p.Leu532Phe(p.L532F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript