Primary Site >> Esophagus Cancer

Gene >> CRMP1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000397890
Start 5856188:5856188(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.433T>C
AA Mutation p.Tyr145His(p.Y145H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000397890
Start 5839541:5839541(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.949T>G
AA Mutation p.Leu317Val(p.L317V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000397890
Start 5835919:5835919(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1277A>G
AA Mutation p.Lys426Arg(p.K426R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000397890
Start 5828541:5828541(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370759908
CDS Mutation c.1409C>T
AA Mutation p.Pro470Leu(p.P470L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000397890
Start 5836899:5836899(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.976T>C
Mutation Classification Silent
Feature Type Transcript