Primary Site >> Stomach Cancer

Gene >> FBXW11

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000265094
Start 171878050:171878050(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.869A>T
AA Mutation p.Glu290Val(p.E290V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000265094
Start 171872938:171872938(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1211G>A
AA Mutation p.Arg404Gln(p.R404Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000265094
Start 171868744:171868744(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1520G>T
AA Mutation p.Ser507Ile(p.S507I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000265094
Start 171868775:171868775(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1489C>T
AA Mutation p.Arg497Trp(p.R497W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000265094
Start 171872908:171872908(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1241G>A
AA Mutation p.Arg414His(p.R414H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000265094
Start 171876493:171876493(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.950T>A
AA Mutation p.Ile317Asn(p.I317N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000265094
Start 171872981:171872981(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1168A>T
AA Mutation p.Thr390Ser(p.T390S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000265094
Start 171878126:171878126(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.793T>C
AA Mutation p.Trp265Arg(p.W265R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000265094
Start 171876377:171876377(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776500801
CDS Mutation c.1066C>T
AA Mutation p.Arg356Cys(p.R356C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000265094
Start 171872909:171872909(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1240C>T
AA Mutation p.Arg414Cys(p.R414C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000265094
Start 171957605:171957605(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.139T>C
AA Mutation p.Cys47Arg(p.C47R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000265094
Start 171899953:171899953(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.521C>T
AA Mutation p.Thr174Ile(p.T174I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000265094
Start 171891493:171891493(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.763A>G
AA Mutation p.Ser255Gly(p.S255G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000265094
Start 171878019:171878019(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.900T>G
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000265094
Start 171872982:171872982(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1167C>T
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000265094
Start 171910636:171910636(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.309G>A
Mutation Classification Silent
Feature Type Transcript
ID 17
Mutation Consequence stop_gained
Transcription ID ENST00000265094
Start 171899966:171899966(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.508C>T
AA Mutation p.Arg170Ter(p.R170*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript