Primary Site >> Stomach Cancer

Gene >> ATXN3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000558190
Start 92064366:92064366(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1040C>A
AA Mutation p.Ser347Tyr(p.S347Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000532032
Start 92082407:92082407(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.668A>G
AA Mutation p.Asp223Gly(p.D223G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000532032
Start 92081025:92081025(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.812C>T
AA Mutation p.Thr271Ile(p.T271I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000532032
Start 92093780:92093780(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.286A>G
AA Mutation p.Ser96Gly(p.S96G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000532032
Start 92093769:92093769(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.297T>C
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000532032
Start 92088745:92088745(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.460C>T
AA Mutation p.Gln154Ter(p.Q154*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript