Primary Site >> Stomach Cancer

Gene >> F12

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000253496
Start 177405123:177405123(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.460G>A
AA Mutation p.Glu154Lys(p.E154K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000253496
Start 177404538:177404538(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.761A>G
AA Mutation p.Gln254Arg(p.Q254R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000253496
Start 177405993:177405993(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.184A>G
AA Mutation p.Thr62Ala(p.T62A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000253496
Start 177403303:177403303(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1482C>A
Mutation Classification Silent
Feature Type Transcript