Colon Cancer: Gene >> RNF152

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312828
Start	61816316:61816316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768728944
CDS Mutation	c.148C>T
AA Mutation	p.Arg50Trp(p.R50W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312828
Start	61816132:61816132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565129525
CDS Mutation	c.332C>T
AA Mutation	p.Ala111Val(p.A111V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312828
Start	61816396:61816396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.68G>A
AA Mutation	p.Arg23His(p.R23H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312828
Start	61816158:61816158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.306G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RNF152

No Mutation Annotation!