Primary Site >> Stomach Cancer

Gene >> WASF2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000618852
Start 27416044:27416044(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.478T>C
AA Mutation p.Trp160Arg(p.W160R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000618852
Start 27419047:27419047(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.172G>A
AA Mutation p.Ala58Thr(p.A58T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000618852
Start 27428877:27428877(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.14C>T
AA Mutation p.Thr5Met(p.T5M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000618852
Start 27418390:27418390(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.298T>A
AA Mutation p.Phe100Ile(p.F100I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000618852
Start 27428809:27428809(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779097597
CDS Mutation c.82G>A
AA Mutation p.Val28Met(p.V28M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000618852
Start 27414905:27414905(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.596G>A
AA Mutation p.Arg199His(p.R199H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000618852
Start 27409849:27409849(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200541363
CDS Mutation c.1182C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000618852
Start 27428783:27428783(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.108C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000618852
Start 27410197:27410197(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.834G>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000618852
Start 27418372:27418372(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.316C>T
AA Mutation p.Gln106Ter(p.Q106*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript