Primary Site >> Esophagus Cancer

Gene >> WNK2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000297954
Start 93308487:93308487(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6530C>T
AA Mutation p.Ala2177Val(p.A2177V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000297954
Start 93317596:93317596(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6704C>T
AA Mutation p.Pro2235Leu(p.P2235L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000297954
Start 93247811:93247811(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781420468
CDS Mutation c.1811C>T
AA Mutation p.Pro604Leu(p.P604L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000297954
Start 93317877:93317877(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768523545
CDS Mutation c.6744C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000297954
Start 93185484:93185484(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.555C>T
Mutation Classification Silent
Feature Type Transcript