Primary Site >> Stomach Cancer

Gene >> PBLD

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000309049
Start 68292223:68292223(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750680281
CDS Mutation c.299C>T
AA Mutation p.Thr100Met(p.T100M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000309049
Start 68284192:68284192(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.852C>G
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000309049
Start 68285367:68285367(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.735G>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000309049
Start 68296288:68296288(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.261A>G
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence inframe_insertion
Transcription ID ENST00000309049
Start 68292191:68292192(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.322_330dupGGAGAACTA
AA Mutation p.Gly108_Leu110dup(p.G108_L110dup)
Mutation Classification In_Frame_Ins
Feature Type Transcript