Colon Cancer: Gene >> CELF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358597
Start	47484406:47484406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.428C>A
AA Mutation	p.Pro143His(p.P143H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358597
Start	47476875:47476875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.974C>T
AA Mutation	p.Thr325Met(p.T325M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358597
Start	47483496:47483496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.482C>T
AA Mutation	p.Ala161Val(p.A161V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358597
Start	47473194:47473194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1227C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_lost
Transcription ID	ENST00000358597
Start	47472232:47472232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1459T>C
AA Mutation	p.Ter487ArgextTer9(p.*487Rext*9)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CELF1

No Mutation Annotation!