Primary Site >> Stomach Cancer

Gene >> FAF1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000396153
Start 50490640:50490640(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1601C>T
AA Mutation p.Ala534Val(p.A534V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000396153
Start 50475558:50475558(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1775C>T
AA Mutation p.Ala592Val(p.A592V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000396153
Start 50655488:50655488(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.698G>A
AA Mutation p.Arg233His(p.R233H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000396153
Start 50801664:50801664(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.128G>A
AA Mutation p.Gly43Asp(p.G43D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000396153
Start 50490632:50490632(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1609T>C
AA Mutation p.Phe537Leu(p.F537L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000396153
Start 50959783:50959783(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.29T>G
AA Mutation p.Ile10Ser(p.I10S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000396153
Start 50583704:50583704(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.979G>A
AA Mutation p.Ala327Thr(p.A327T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000396153
Start 50788072:50788072(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750800804
CDS Mutation c.295C>T
AA Mutation p.Arg99Trp(p.R99W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000396153
Start 50584705:50584705(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.947C>T
AA Mutation p.Ala316Val(p.A316V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000396153
Start 50539650:50539650(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750398957
CDS Mutation c.1347G>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000396153
Start 50475584:50475584(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1749C>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000396153
Start 50539663:50539664(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1333dupA
AA Mutation p.Thr445AsnfsTer17(p.T445Nfs*17)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000396153
Start 50738922:50738923(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.491dupA
AA Mutation p.Asn164LysfsTer18(p.N164Kfs*18)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 14
Mutation Consequence splice_donor_variant
Transcription ID ENST00000396153
Start 50857927:50857927(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.114+2T>C
Mutation Classification Splice_Site
Feature Type Transcript