Primary Site >> Stomach Cancer

Gene >> STAC3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000332782
Start 57249127:57249127(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.248A>G
AA Mutation p.Lys83Arg(p.K83R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000332782
Start 57249064:57249064(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.311A>G
AA Mutation p.Asp104Gly(p.D104G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000332782
Start 57245205:57245205(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.610G>T
AA Mutation p.Ala204Ser(p.A204S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000332782
Start 57246886:57246886(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.521A>G
AA Mutation p.Asn174Ser(p.N174S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000332782
Start 57249118:57249118(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764988214
CDS Mutation c.257A>G
AA Mutation p.Asn86Ser(p.N86S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000332782
Start 57244205:57244205(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.879C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000332782
Start 57249222:57249222(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.153G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000332782
Start 57244961:57244961(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.675C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000332782
Start 57243860:57243860(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1047C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000332782
Start 57244601:57244601(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.742C>T
AA Mutation p.Gln248Ter(p.Q248*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript