Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PSPH

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000275605
Start 56019691:56019691(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.184C>G
AA Mutation p.Leu62Val(p.L62V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000275605
Start 56021085:56021085(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201419960
CDS Mutation c.128C>T
AA Mutation p.Ala43Val(p.A43V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000275605
Start 56021144:56021144(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.69C>T
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> PSPH

No Mutation Annotation!