Primary Site >> Esophagus Cancer

Gene >> PLEKHG5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000400915
Start 6474063:6474063(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.709G>T
AA Mutation p.Ala237Ser(p.A237S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000400915
Start 6470331:6470331(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1873G>C
AA Mutation p.Asp625His(p.D625H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000400915
Start 6467883:6467883(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3121C>G
AA Mutation p.Leu1041Val(p.L1041V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000400915
Start 6470759:6470759(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1686C>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000400915
Start 6473145:6473145(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.993C>A
Mutation Classification Silent
Feature Type Transcript