Colon Cancer: Gene >> DUS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358896
Start	68078452:68078452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1178G>A
AA Mutation	p.Arg393His(p.R393H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358896
Start	68053652:68053652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.261G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358896
Start	68053595:68053595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.204T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358896
Start	68053626:68053626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.235A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358896
Start	68049540:68049540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751776821
CDS Mutation	c.162A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DUS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358896
Start	68076661:68076661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1112A>T
AA Mutation	p.Lys371Met(p.K371M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript