Primary Site >> Esophagus Cancer

Gene >> LATS2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000382592
Start 20988039:20988039(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775892552
CDS Mutation c.1741C>T
AA Mutation p.Arg581Cys(p.R581C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000382592
Start 20983707:20983707(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145120725
CDS Mutation c.1999A>G
AA Mutation p.Met667Val(p.M667V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000382592
Start 20981594:20981594(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2537C>T
AA Mutation p.Ser846Phe(p.S846F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000382592
Start 20988117:20988117(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1663G>T
AA Mutation p.Asp555Tyr(p.D555Y)
Mutation Classification Missense_Mutation
Feature Type Transcript