Primary Site >> Stomach Cancer

Gene >> XAF1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000361842
Start 6770674:6770674(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.539A>C
AA Mutation p.Lys180Thr(p.K180T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000361842
Start 6770731:6770731(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.596C>T
AA Mutation p.Ala199Val(p.A199V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000361842
Start 6770965:6770965(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.830C>T
AA Mutation p.Pro277Leu(p.P277L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000361842
Start 6760553:6760553(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372380890
CDS Mutation c.373G>A
AA Mutation p.Ala125Thr(p.A125T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000361842
Start 6770749:6770749(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371250443
CDS Mutation c.614C>T
AA Mutation p.Thr205Met(p.T205M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000361842
Start 6758132:6758132(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.76T>C
AA Mutation p.Tyr26His(p.Y26H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000361842
Start 6758104:6758104(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.48C>T
Mutation Classification Silent
Feature Type Transcript