Primary Site >> Stomach Cancer

Gene >> FYN

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000354650
Start 111702930:111702930(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.652C>T
AA Mutation p.Arg218Trp(p.R218W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000354650
Start 111702966:111702966(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.616C>T
AA Mutation p.Arg206Cys(p.R206C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000354650
Start 111674621:111674621(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1283T>G
AA Mutation p.Phe428Cys(p.F428C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000354650
Start 111719934:111719934(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.118C>T
AA Mutation p.Pro40Ser(p.P40S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000354650
Start 111674589:111674589(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1315C>A
AA Mutation p.Leu439Met(p.L439M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000354650
Start 111674510:111674510(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1394T>C
AA Mutation p.Val465Ala(p.V465A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000354650
Start 111694492:111694492(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1156T>C
AA Mutation p.Tyr386His(p.Y386H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000354650
Start 111661902:111661902(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1451G>T
AA Mutation p.Arg484Met(p.R484M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000354650
Start 111694473:111694473(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1175G>A
AA Mutation p.Arg392Gln(p.R392Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000354650
Start 111708011:111708011(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.354T>C
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000354650
Start 111714439:111714439(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.252G>A
Mutation Classification Silent
Feature Type Transcript