Primary Site >> Stomach Cancer

Gene >> HAS3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000306560
Start 69114482:69114482(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.878G>C
AA Mutation p.Ser293Thr(p.S293T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000306560
Start 69109724:69109724(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372849295
CDS Mutation c.329G>A
AA Mutation p.Arg110His(p.R110H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000306560
Start 69114409:69114409(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.805G>A
AA Mutation p.Val269Met(p.V269M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000306560
Start 69109539:69109539(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371823602
CDS Mutation c.144C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000306560
Start 69109917:69109917(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767800507
CDS Mutation c.522G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000306560
Start 69114816:69114816(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1212C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000306560
Start 69109785:69109785(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.390C>A
Mutation Classification Silent
Feature Type Transcript