Colon Cancer: Gene >> RNF138

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000261593
Start	32092885:32092885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.109G>A
AA Mutation	p.Val37Ile(p.V37I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261593
Start	32113764:32113764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.296G>A
AA Mutation	p.Arg99Lys(p.R99K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261593
Start	32126787:32126787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.656A>G
AA Mutation	p.Tyr219Cys(p.Y219C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261593
Start	32111815:32111815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.172C>T
AA Mutation	p.Arg58Cys(p.R58C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261593
Start	32113837:32113837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751628139
CDS Mutation	c.369C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RNF138

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261593
Start	32126772:32126772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.641G>T
AA Mutation	p.Arg214Ile(p.R214I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript