Primary Site >> Stomach Cancer

Gene >> OTUD7B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000581312
Start 149944759:149944759(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782204756
CDS Mutation c.1630G>A
AA Mutation p.Gly544Ser(p.G544S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000581312
Start 149944084:149944084(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2305T>C
AA Mutation p.Tyr769His(p.Y769H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000581312
Start 149967516:149967516(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753757221
CDS Mutation c.280C>T
AA Mutation p.Arg94Cys(p.R94C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000581312
Start 149944939:149944939(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782602473
CDS Mutation c.1450C>T
AA Mutation p.Arg484Trp(p.R484W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000581312
Start 149944500:149944500(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782033576
CDS Mutation c.1889G>A
AA Mutation p.Arg630His(p.R630H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000581312
Start 149949748:149949748(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782789210
CDS Mutation c.1004A>G
AA Mutation p.Tyr335Cys(p.Y335C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000581312
Start 149944255:149944255(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369467490
CDS Mutation c.2134C>T
AA Mutation p.Arg712Trp(p.R712W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000581312
Start 149971098:149971098(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.239G>A
AA Mutation p.Arg80Gln(p.R80Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000581312
Start 149944945:149944945(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369849263
CDS Mutation c.1444G>A
AA Mutation p.Gly482Ser(p.G482S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000581312
Start 149977501:149977501(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10G>A
AA Mutation p.Asp4Asn(p.D4N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000581312
Start 149944894:149944894(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1495G>A
AA Mutation p.Ala499Thr(p.A499T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000581312
Start 149959707:149959707(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.822T>C
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000581312
Start 149944877:149944877(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1512C>T
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000581312
Start 149944728:149944728(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1661delA
AA Mutation p.Asn554ThrfsTer3(p.N554Tfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000581312
Start 149944085:149944085(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2304delC
AA Mutation p.Tyr769ThrfsTer59(p.Y769Tfs*59)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000581312
Start 149944423:149944423(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1966G>T
AA Mutation p.Gly656Ter(p.G656*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript