Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PDE6D

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000287600
Start 231738055:231738055(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758019119
CDS Mutation c.223C>T
AA Mutation p.Arg75Cys(p.R75C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000287600
Start 231738078:231738078(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.200C>T
AA Mutation p.Ser67Leu(p.S67L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000287600
Start 231738023:231738023(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.255A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000287600
Start 231737282:231737282(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs571686278
CDS Mutation c.276C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence stop_gained
Transcription ID ENST00000287600
Start 231737243:231737243(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.315G>A
AA Mutation p.Trp105Ter(p.W105*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> PDE6D

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000287600
Start 231738120:231738120(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.158T>A
AA Mutation p.Ile53Asn(p.I53N)
Mutation Classification Missense_Mutation
Feature Type Transcript