Primary Site >> Esophagus Cancer

Gene >> INSR

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000302850
Start 7152777:7152777(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2180C>T
AA Mutation p.Ser727Leu(p.S727L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000302850
Start 7152804:7152804(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2153A>G
AA Mutation p.Gln718Arg(p.Q718R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000302850
Start 7125381:7125381(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3160G>A
AA Mutation p.Val1054Met(p.V1054M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000302850
Start 7168020:7168020(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1558T>C
AA Mutation p.Trp520Arg(p.W520R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000302850
Start 7166273:7166273(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747464322
CDS Mutation c.1742G>A
AA Mutation p.Arg581Gln(p.R581Q)
Mutation Classification Missense_Mutation
Feature Type Transcript