Primary Site >> Stomach Cancer

Gene >> USP44

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000258499
Start 95533880:95533880(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.377G>A
AA Mutation p.Gly126Asp(p.G126D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000258499
Start 95533059:95533059(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1198G>T
AA Mutation p.Val400Phe(p.V400F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000258499
Start 95521192:95521192(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752458868
CDS Mutation c.1744C>T
AA Mutation p.Arg582Cys(p.R582C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000258499
Start 95524723:95524723(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745410068
CDS Mutation c.1690T>C
AA Mutation p.Cys564Arg(p.C564R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000258499
Start 95524782:95524782(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372529431
CDS Mutation c.1631G>A
AA Mutation p.Arg544His(p.R544H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000258499
Start 95533958:95533958(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144639311
CDS Mutation c.299G>A
AA Mutation p.Arg100His(p.R100H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000258499
Start 95533592:95533592(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762034925
CDS Mutation c.665C>T
AA Mutation p.Ser222Leu(p.S222L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000258499
Start 95533093:95533093(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1164G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000258499
Start 95534022:95534022(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.235delT
AA Mutation p.Cys79ValfsTer9(p.C79Vfs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000258499
Start 95533242:95533242(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1015G>T
AA Mutation p.Glu339Ter(p.E339*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000258499
Start 95534021:95534022(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.235dupT
AA Mutation p.Cys79LeufsTer5(p.C79Lfs*5)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript