Colon Cancer: Gene >> CLEC3B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296130
Start	45035772:45035772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.457G>C
AA Mutation	p.Ala153Pro(p.A153P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296130
Start	45026454:45026454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.92T>G
AA Mutation	p.Ile31Ser(p.I31S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296130
Start	45035872:45035872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.557A>G
AA Mutation	p.Asp186Gly(p.D186G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296130
Start	45035798:45035798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.483C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296130
Start	45035771:45035771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.456C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296130
Start	45035834:45035834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.519C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CLEC3B

No Mutation Annotation!