Primary Site >> Stomach Cancer

Gene >> FTO

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000471389
Start 53826299:53826299(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.559G>C
AA Mutation p.Gly187Arg(p.G187R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000471389
Start 53873836:53873836(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777196899
CDS Mutation c.946C>T
AA Mutation p.Arg316Trp(p.R316W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000471389
Start 53826029:53826029(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368658799
CDS Mutation c.289A>G
AA Mutation p.Ile97Val(p.I97V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000471389
Start 53879879:53879879(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1011C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000471389
Start 54111771:54111771(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1374A>G
Mutation Classification Silent
Feature Type Transcript