Primary Site >> Stomach Cancer

Gene >> FAM107B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000181796
Start 14774398:14774398(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.266C>T
AA Mutation p.Ala89Val(p.A89V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000378458
Start 14521303:14521303(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.283G>A
AA Mutation p.Glu95Lys(p.E95K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000378458
Start 14530426:14530426(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.34C>T
AA Mutation p.Pro12Ser(p.P12S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000181796
Start 14774404:14774404(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.260G>A
AA Mutation p.Gly87Asp(p.G87D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000181796
Start 14774492:14774492(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.172G>A
AA Mutation p.Ala58Thr(p.A58T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000181796
Start 14774292:14774292(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.372C>T
Mutation Classification Silent
Feature Type Transcript