Primary Site >> Esophagus Cancer

Gene >> LRP6

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261349
Start 12159870:12159870(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2374C>T
AA Mutation p.Arg792Trp(p.R792W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261349
Start 12126894:12126894(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4109C>A
AA Mutation p.Ala1370Asp(p.A1370D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000261349
Start 12126791:12126791(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4212A>G
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000261349
Start 12186963:12186963(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.804C>G
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000261349
Start 12158888:12158888(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2732delG
AA Mutation p.Gly911ValfsTer38(p.G911Vfs*38)
Mutation Classification Frame_Shift_Del
Feature Type Transcript