Colon Cancer: Gene >> FUZ

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313777
Start	49809502:49809502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.566C>T
AA Mutation	p.Ala189Val(p.A189V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313777
Start	49807242:49807242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779762408
CDS Mutation	c.1166G>T
AA Mutation	p.Arg389Leu(p.R389L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313777
Start	49809472:49809472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.596C>T
AA Mutation	p.Thr199Met(p.T199M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313777
Start	49809570:49809570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.498C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313777
Start	49813020:49813020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.87C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000313777
Start	49807198:49807198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200831588
CDS Mutation	c.1210C>T
AA Mutation	p.Arg404Ter(p.R404*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FUZ

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313777
Start	49808464:49808464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.983G>A
AA Mutation	p.Arg328His(p.R328H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313777
Start	49811637:49811637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.381C>T
Mutation Classification	Silent
Feature Type	Transcript