Primary Site >> Stomach Cancer

Gene >> PYGO2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368457
Start 154959029:154959029(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.971C>T
AA Mutation p.Pro324Leu(p.P324L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000368457
Start 154959470:154959470(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.530C>A
AA Mutation p.Pro177His(p.P177H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000368457
Start 154958874:154958874(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1126G>A
AA Mutation p.Val376Ile(p.V376I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000368457
Start 154959505:154959505(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.495A>G
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000368457
Start 154959745:154959745(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.255delC
AA Mutation p.Val87TrpfsTer74(p.V87Wfs*74)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000368457
Start 154959595:154959595(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.405delC
AA Mutation p.Phe136SerfsTer25(p.F136Sfs*25)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000368457
Start 154959552:154959552(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.448delC
AA Mutation p.Gln150ArgfsTer11(p.Q150Rfs*11)
Mutation Classification Frame_Shift_Del
Feature Type Transcript