Colon Cancer: Gene >> CSN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000353151
Start	69957531:69957531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418C>A
AA Mutation	p.His140Asn(p.H140N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000353151
Start	69957745:69957745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146872617
CDS Mutation	c.204C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000353151
Start	69957682:69957682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.267G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000353151
Start	69957474:69957479(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.470_475delTTCCTC
AA Mutation	p.Ile157_Gln159delinsLys(p.I157_Q159delinsK)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CSN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000353151
Start	69957621:69957621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767421388
CDS Mutation	c.328A>G
AA Mutation	p.Thr110Ala(p.T110A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript