ClinVar Miner

List of variants in gene PSMB4 reported as likely benign for not provided

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 94
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HGVS dbSNP gnomAD frequency
NM_002796.3(PSMB4):c.336C>T (p.Leu112=) rs11557389 0.00196
NM_002796.3(PSMB4):c.705C>T (p.Ala235=) rs116353887 0.00046
NM_002796.3(PSMB4):c.2T>C (p.Met1Thr) rs199968815 0.00026
NM_002796.3(PSMB4):c.300C>T (p.Gly100=) rs6684391 0.00017
NM_002796.3(PSMB4):c.782+20T>C rs373666677 0.00012
NM_002796.3(PSMB4):c.141-9A>T rs780661377 0.00008
NM_002796.3(PSMB4):c.337G>A (p.Gly113Ser) rs372581320 0.00006
NM_002796.3(PSMB4):c.652A>G (p.Met218Val) rs115063024 0.00006
NM_002796.3(PSMB4):c.141-16C>T rs767892782 0.00005
NM_002796.3(PSMB4):c.577-6C>G rs769580817 0.00005
NM_002796.3(PSMB4):c.39G>T (p.Ala13=) rs149809535 0.00004
NM_002796.3(PSMB4):c.576+11A>C rs749821154 0.00003
NM_002796.3(PSMB4):c.702C>T (p.Ile234=) rs540582656 0.00003
NM_002796.3(PSMB4):c.141-15G>A rs753263289 0.00002
NM_002796.3(PSMB4):c.480T>C (p.Tyr160=) rs1235645157 0.00002
NM_002796.3(PSMB4):c.577-14C>T rs772103438 0.00002
NM_002796.3(PSMB4):c.663G>A (p.Leu221=) rs536032032 0.00002
NM_002796.3(PSMB4):c.693+16G>A rs1199604305 0.00002
NM_002796.3(PSMB4):c.138C>T (p.Thr46=) rs769914025 0.00001
NM_002796.3(PSMB4):c.140+13C>A rs777961225 0.00001
NM_002796.3(PSMB4):c.141-14T>C rs184144161 0.00001
NM_002796.3(PSMB4):c.141-17C>A rs971839970 0.00001
NM_002796.3(PSMB4):c.348-11T>C rs923115397 0.00001
NM_002796.3(PSMB4):c.348-14C>G rs1191688043 0.00001
NM_002796.3(PSMB4):c.494+14C>T rs1012419260 0.00001
NM_002796.3(PSMB4):c.576+8G>T rs1246043756 0.00001
NM_002796.3(PSMB4):c.576+8_576+9del rs1652794372 0.00001
NM_002796.3(PSMB4):c.576+9dup rs111362043 0.00001
NM_002796.3(PSMB4):c.582G>A (p.Leu194=) rs1408957796 0.00001
NM_002796.3(PSMB4):c.583C>T (p.Leu195=) rs766279607 0.00001
NM_002796.3(PSMB4):c.693+10G>A rs1380743843 0.00001
NM_002796.3(PSMB4):c.693+8A>G rs750893123 0.00001
NM_002796.3(PSMB4):c.694-18T>C rs1186002436 0.00001
NM_002796.3(PSMB4):c.694-4C>A rs148669878 0.00001
NM_002796.3(PSMB4):c.694-6T>C rs763498969 0.00001
NM_002796.3(PSMB4):c.782+18A>T rs746902065 0.00001
NM_002796.3(PSMB4):c.782+19A>G rs1652846273 0.00001
NM_002796.3(PSMB4):c.105G>C (p.Ala35=) rs2102121176
NM_002796.3(PSMB4):c.108T>C (p.Ser36=)
NM_002796.3(PSMB4):c.111A>C (p.Ala37=)
NM_002796.3(PSMB4):c.13T>C (p.Leu5=) rs2102121007
NM_002796.3(PSMB4):c.140+19C>T rs1449210366
NM_002796.3(PSMB4):c.141-9A>C rs780661377
NM_002796.3(PSMB4):c.141-9_141-6del rs775025489
NM_002796.3(PSMB4):c.171C>T (p.Leu57=) rs768552789
NM_002796.3(PSMB4):c.174C>G (p.Gly58=) rs1571304854
NM_002796.3(PSMB4):c.183C>T (p.Phe61=) rs1571304866
NM_002796.3(PSMB4):c.258C>T (p.Arg86=)
NM_002796.3(PSMB4):c.286C>T (p.Leu96=) rs1571304933
NM_002796.3(PSMB4):c.309T>C (p.Ala103=) rs2529156684
NM_002796.3(PSMB4):c.321T>C (p.Tyr107=) rs2529156723
NM_002796.3(PSMB4):c.347+15G>C rs202128210
NM_002796.3(PSMB4):c.347+15G>T rs202128210
NM_002796.3(PSMB4):c.347+17A>G
NM_002796.3(PSMB4):c.347+20G>A
NM_002796.3(PSMB4):c.348-8C>T
NM_002796.3(PSMB4):c.39G>A (p.Ala13=) rs149809535
NM_002796.3(PSMB4):c.39G>C (p.Ala13=)
NM_002796.3(PSMB4):c.435C>T (p.Arg145=)
NM_002796.3(PSMB4):c.438G>C (p.Ser146=) rs1176744494
NM_002796.3(PSMB4):c.471C>T (p.Ile157=) rs751892201
NM_002796.3(PSMB4):c.48G>A (p.Pro16=)
NM_002796.3(PSMB4):c.494+17del rs765134636
NM_002796.3(PSMB4):c.576+20G>A rs986334668
NM_002796.3(PSMB4):c.577-5C>T rs2102122945
NM_002796.3(PSMB4):c.606G>A (p.Gln202=)
NM_002796.3(PSMB4):c.624C>T (p.Thr208=) rs1007493165
NM_002796.3(PSMB4):c.666C>T (p.Tyr222=) rs1553209373
NM_002796.3(PSMB4):c.672A>G (p.Arg224=)
NM_002796.3(PSMB4):c.690C>T (p.Asn230=) rs765709131
NM_002796.3(PSMB4):c.693+15G>C rs758858496
NM_002796.3(PSMB4):c.693+15G>T rs758858496
NM_002796.3(PSMB4):c.693+19A>G
NM_002796.3(PSMB4):c.694-10T>C rs1386774986
NM_002796.3(PSMB4):c.694-11C>T rs2529161476
NM_002796.3(PSMB4):c.694-12_694-10del rs755122811
NM_002796.3(PSMB4):c.694-12_694-9del rs2529161467
NM_002796.3(PSMB4):c.694-20A>C
NM_002796.3(PSMB4):c.694-20_694-17del rs1428345745
NM_002796.3(PSMB4):c.694-7C>T rs377316848
NM_002796.3(PSMB4):c.699A>G (p.Gln233=)
NM_002796.3(PSMB4):c.701_702delinsCT (p.Ile234Thr) rs2102123564
NM_002796.3(PSMB4):c.702C>A (p.Ile234=)
NM_002796.3(PSMB4):c.714C>G (p.Thr238=) rs775286900
NM_002796.3(PSMB4):c.742T>C (p.Leu248=) rs1652841131
NM_002796.3(PSMB4):c.771C>A (p.Ala257=) rs760061076
NM_002796.3(PSMB4):c.782+10A>G rs754155948
NM_002796.3(PSMB4):c.782+11G>A rs146720393
NM_002796.3(PSMB4):c.782+20T>G rs373666677
NM_002796.3(PSMB4):c.782+8A>G rs2529161911
NM_002796.3(PSMB4):c.783-10_783-7del rs768274893
NM_002796.3(PSMB4):c.783-15_783-12del rs557553474
NM_002796.3(PSMB4):c.783-7T>G rs764240505
NM_002796.3(PSMB4):c.786C>T (p.Gly262=) rs2102124056

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