Primary Site >> Stomach Cancer

Gene >> FGF12

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000454309
Start 192335459:192335459(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.316T>C
AA Mutation p.Phe106Leu(p.F106L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000454309
Start 192144077:192144077(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.664C>T
AA Mutation p.Arg222Cys(p.R222C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000454309
Start 192408091:192408091(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766226672
CDS Mutation c.133G>A
AA Mutation p.Val45Ile(p.V45I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000454309
Start 192170567:192170567(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.504A>T
AA Mutation p.Glu168Asp(p.E168D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000454309
Start 192408042:192408042(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.182C>A
AA Mutation p.Pro61Gln(p.P61Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000454309
Start 192335456:192335456(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.319A>C
AA Mutation p.Asn107His(p.N107H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000454309
Start 192408042:192408042(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.182C>T
AA Mutation p.Pro61Leu(p.P61L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000454309
Start 192170502:192170502(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.569A>G
AA Mutation p.Lys190Arg(p.K190R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000454309
Start 192144060:192144060(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.681T>C
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000454309
Start 192170507:192170507(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.564A>G
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000454309
Start 192408149:192408149(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.75G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000454309
Start 192408056:192408056(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.168C>T
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence stop_gained
Transcription ID ENST00000454309
Start 192335420:192335420(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.355C>T
AA Mutation p.Gln119Ter(p.Q119*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript