Primary Site >> Stomach Cancer

Gene >> USP14

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261601
Start 211247:211247(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757981348
CDS Mutation c.1448G>A
AA Mutation p.Arg483His(p.R483H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261601
Start 196666:196666(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.493A>G
AA Mutation p.Lys165Glu(p.K165E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261601
Start 196733:196733(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.560C>T
AA Mutation p.Ala187Val(p.A187V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000261601
Start 211172:211172(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1373T>C
AA Mutation p.Val458Ala(p.V458A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000261601
Start 196658:196658(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.485C>T
AA Mutation p.Ser162Phe(p.S162F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000261601
Start 211160:211160(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1361A>C
AA Mutation p.Lys454Thr(p.K454T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000261601
Start 166813:166813(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.194delA
AA Mutation p.Asn65MetfsTer3(p.N65Mfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000261601
Start 209989:209989(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1186delC
AA Mutation p.Gln396ArgfsTer29(p.Q396Rfs*29)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000261601
Start 203146:203146(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.997delT
AA Mutation p.Tyr333IlefsTer7(p.Y333Ifs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000261601
Start 203145:203146(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.997dupT
AA Mutation p.Tyr333LeufsTer2(p.Y333Lfs*2)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript