Primary Site >> Stomach Cancer

Gene >> FOXF2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000259806
Start 1390312:1390312(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.365C>T
AA Mutation p.Thr122Met(p.T122M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000259806
Start 1390249:1390249(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.302C>T
AA Mutation p.Pro101Leu(p.P101L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000259806
Start 1390574:1390574(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.627C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000259806
Start 1390250:1390250(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.303G>A
Mutation Classification Silent
Feature Type Transcript