Colon Cancer: Gene >> CCND2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261254
Start	4276127:4276127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.318G>C
AA Mutation	p.Met106Ile(p.M106I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261254
Start	4288876:4288876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199552192
CDS Mutation	c.606C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261254
Start	4288870:4288870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562182290
CDS Mutation	c.600G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261254
Start	4276088:4276088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.279T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261254
Start	4288867:4288867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747054950
CDS Mutation	c.597G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CCND2

No Mutation Annotation!