Colon Cancer: Gene >> RPN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000237530
Start	37184332:37184332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146095088
CDS Mutation	c.166G>A
AA Mutation	p.Val56Met(p.V56M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000237530
Start	37184291:37184291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.125A>G
AA Mutation	p.Asp42Gly(p.D42G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000237530
Start	37225745:37225745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752016809
CDS Mutation	c.1242C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000237530
Start	37204794:37204794(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.587delG
AA Mutation	p.Gly196AlafsTer41(p.G196Afs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RPN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000237530
Start	37199113:37199113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.367A>G
AA Mutation	p.Thr123Ala(p.T123A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000237530
Start	37228621:37228621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747878354
CDS Mutation	c.1371C>T
Mutation Classification	Silent
Feature Type	Transcript