Primary Site >> Stomach Cancer

Gene >> FRK

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000606080
Start 115967659:115967659(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750533470
CDS Mutation c.691C>T
AA Mutation p.Arg231Cys(p.R231C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000606080
Start 116060301:116060301(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11T>C
AA Mutation p.Ile4Thr(p.I4T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000606080
Start 115956586:115956586(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.824T>C
AA Mutation p.Leu275Pro(p.L275P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000606080
Start 116003932:116003932(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375756617
CDS Mutation c.411C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000606080
Start 115968627:115968627(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371241978
CDS Mutation c.579C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000606080
Start 116003896:116003896(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.447delA
AA Mutation p.Gly150GlufsTer8(p.G150Efs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript