Primary Site >> Stomach Cancer

Gene >> FH

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000366560
Start 241517241:241517241(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs587782207
CDS Mutation c.208G>A
AA Mutation p.Ala70Thr(p.A70T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000366560
Start 241517222:241517222(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778578307
CDS Mutation c.227C>T
AA Mutation p.Thr76Met(p.T76M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000366560
Start 241504167:241504167(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.983T>C
AA Mutation p.Met328Thr(p.M328T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000366560
Start 241504075:241504075(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1075C>G
AA Mutation p.Pro359Ala(p.P359A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000366560
Start 241508768:241508768(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.573T>C
Mutation Classification Silent
Feature Type Transcript