Primary Site >> Stomach Cancer

Gene >> FAM3B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000357985
Start 41322974:41322974(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.71C>T
AA Mutation p.Ser24Leu(p.S24L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000357985
Start 41338476:41338476(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs556115707
CDS Mutation c.262G>A
AA Mutation p.Ala88Thr(p.A88T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000357985
Start 41338432:41338432(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.218C>G
AA Mutation p.Thr73Ser(p.T73S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000357985
Start 41347047:41347047(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.432T>C
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000357985
Start 41338392:41338392(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.178A>C
Mutation Classification Silent
Feature Type Transcript