Primary Site >> Esophagus Cancer

Gene >> GHR

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000230882
Start 42719054:42719054(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1547T>C
AA Mutation p.Met516Thr(p.M516T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000230882
Start 42629067:42629067(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.100T>C
AA Mutation p.Trp34Arg(p.W34R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000230882
Start 42719217:42719217(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1710A>G
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000230882
Start 42718620:42718620(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1113G>A
Mutation Classification Silent
Feature Type Transcript