Primary Site >> Stomach Cancer

Gene >> FARP2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264042
Start 241462539:241462539(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1604A>G
AA Mutation p.Glu535Gly(p.E535G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264042
Start 241436522:241436522(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1142C>T
AA Mutation p.Ala381Val(p.A381V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264042
Start 241493360:241493360(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs147747781
CDS Mutation c.2963G>A
AA Mutation p.Gly988Asp(p.G988D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000264042
Start 241492930:241492930(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2789A>G
AA Mutation p.Asn930Ser(p.N930S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000264042
Start 241436506:241436506(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372605073
CDS Mutation c.1126G>A
AA Mutation p.Val376Ile(p.V376I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000264042
Start 241436494:241436494(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1114A>G
AA Mutation p.Thr372Ala(p.T372A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000264042
Start 241493320:241493320(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2923C>T
Mutation Classification Silent
Feature Type Transcript