Primary Site >> Esophagus Cancer

Gene >> THBS2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000366787
Start 169237771:169237771(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1154C>G
AA Mutation p.Ser385Cys(p.S385C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000366787
Start 169222364:169222364(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138017175
CDS Mutation c.3106C>T
AA Mutation p.Arg1036Cys(p.R1036C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000366787
Start 169248850:169248850(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.176G>A
AA Mutation p.Arg59His(p.R59H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000366787
Start 169234852:169234852(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767154900
CDS Mutation c.1533C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000366787
Start 169222332:169222332(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750861595
CDS Mutation c.3138G>A
Mutation Classification Silent
Feature Type Transcript