Primary Site >> Esophagus Cancer

Gene >> PRL

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000306482
Start 22287427:22287427(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779422396
CDS Mutation c.659G>A
AA Mutation p.Arg220Gln(p.R220Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000306482
Start 22287442:22287442(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.644A>G
AA Mutation p.Lys215Arg(p.K215R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000306482
Start 22292586:22292586(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.264T>G
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000306482
Start 22290264:22290264(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.402A>G
Mutation Classification Silent
Feature Type Transcript