Primary Site >> Stomach Cancer

Gene >> NMBR

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000258042
Start 142078599:142078599(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs147317413
CDS Mutation c.727G>A
AA Mutation p.Ala243Thr(p.A243T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000258042
Start 142088315:142088315(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.344G>A
AA Mutation p.Gly115Asp(p.G115D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000258042
Start 142078890:142078890(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141190379
CDS Mutation c.436G>A
AA Mutation p.Val146Ile(p.V146I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000258042
Start 142088628:142088628(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.31G>A
AA Mutation p.Val11Met(p.V11M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000258042
Start 142088430:142088430(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.229G>A
AA Mutation p.Val77Ile(p.V77I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000258042
Start 142088566:142088566(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.93G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000258042
Start 142088518:142088518(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.141G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000258042
Start 142088560:142088560(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.99G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000258042
Start 142088359:142088359(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.300C>T
Mutation Classification Silent
Feature Type Transcript