Primary Site >> Esophagus Cancer

Gene >> LAMC2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264144
Start 183215582:183215582(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.398G>A
AA Mutation p.Arg133Lys(p.R133K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000264144
Start 183227588:183227588(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1359G>A
Mutation Classification Silent
Feature Type Transcript