Primary Site >> Stomach Cancer

Gene >> MEOX2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262041
Start 15685914:15685914(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.489C>A
AA Mutation p.Ser163Arg(p.S163R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262041
Start 15686363:15686363(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.40G>A
AA Mutation p.Ala14Thr(p.A14T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000262041
Start 15626878:15626878(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.558A>T
AA Mutation p.Lys186Asn(p.K186N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000262041
Start 15612396:15612396(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777058351
CDS Mutation c.906G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000262041
Start 15612543:15612543(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755958618
CDS Mutation c.759G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000262041
Start 15686031:15686031(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.372G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000262041
Start 15685971:15685971(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.432C>T
Mutation Classification Silent
Feature Type Transcript