Primary Site >> Stomach Cancer

Gene >> FBLN5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000342058
Start 91877492:91877492(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1180A>G
AA Mutation p.Met394Val(p.M394V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000342058
Start 91887280:91887280(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774458799
CDS Mutation c.652G>A
AA Mutation p.Val218Met(p.V218M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000342058
Start 91937096:91937096(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760345539
CDS Mutation c.230G>A
AA Mutation p.Arg77Gln(p.R77Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000342058
Start 91881411:91881411(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374301196
CDS Mutation c.870C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000342058
Start 91887293:91887293(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753386917
CDS Mutation c.639C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000342058
Start 91940608:91940608(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.81C>T
Mutation Classification Silent
Feature Type Transcript