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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 94

Download table as spreadsheet

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	0.00049
NM_002796.3(PSMB4):c.300C>T (p.Gly100=)	rs6684391	0.00019
NM_002796.3(PSMB4):c.141-15G>A	rs753263289	0.00013
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.39G>T (p.Ala13=)	rs149809535	0.00004
NM_002796.3(PSMB4):c.141-17C>A	rs971839970	0.00001
NM_002796.3(PSMB4):c.171C>T (p.Leu57=)	rs768552789	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.782+18A>T	rs746902065	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.138C>T (p.Thr46=)
NM_002796.3(PSMB4):c.13T>C (p.Leu5=)	rs2102121007
NM_002796.3(PSMB4):c.140+13C>A
NM_002796.3(PSMB4):c.140+19C>T
NM_002796.3(PSMB4):c.141-14T>C
NM_002796.3(PSMB4):c.141-9A>C
NM_002796.3(PSMB4):c.141-9_141-6del
NM_002796.3(PSMB4):c.174C>G (p.Gly58=)
NM_002796.3(PSMB4):c.183C>T (p.Phe61=)
NM_002796.3(PSMB4):c.258C>T (p.Arg86=)
NM_002796.3(PSMB4):c.286C>T (p.Leu96=)	rs1571304933
NM_002796.3(PSMB4):c.2T>C (p.Met1Thr)
NM_002796.3(PSMB4):c.309T>C (p.Ala103=)
NM_002796.3(PSMB4):c.321T>C (p.Tyr107=)
NM_002796.3(PSMB4):c.347+15G>C
NM_002796.3(PSMB4):c.347+15G>T
NM_002796.3(PSMB4):c.347+17A>G
NM_002796.3(PSMB4):c.347+20G>A
NM_002796.3(PSMB4):c.348-11T>C
NM_002796.3(PSMB4):c.348-14C>G
NM_002796.3(PSMB4):c.348-8C>T
NM_002796.3(PSMB4):c.39G>A (p.Ala13=)
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=)
NM_002796.3(PSMB4):c.471C>T (p.Ile157=)
NM_002796.3(PSMB4):c.480T>C (p.Tyr160=)
NM_002796.3(PSMB4):c.48G>A (p.Pro16=)
NM_002796.3(PSMB4):c.494+17del
NM_002796.3(PSMB4):c.576+11A>C
NM_002796.3(PSMB4):c.576+20G>A
NM_002796.3(PSMB4):c.576+8_576+9del
NM_002796.3(PSMB4):c.576+9dup
NM_002796.3(PSMB4):c.577-14C>T
NM_002796.3(PSMB4):c.577-5C>T	rs2102122945
NM_002796.3(PSMB4):c.577-6C>G
NM_002796.3(PSMB4):c.582G>A (p.Leu194=)
NM_002796.3(PSMB4):c.583C>T (p.Leu195=)	rs766279607
NM_002796.3(PSMB4):c.606G>A (p.Gln202=)
NM_002796.3(PSMB4):c.624C>T (p.Thr208=)
NM_002796.3(PSMB4):c.663G>A (p.Leu221=)
NM_002796.3(PSMB4):c.666C>T (p.Tyr222=)
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+10G>A
NM_002796.3(PSMB4):c.693+15G>C
NM_002796.3(PSMB4):c.693+15G>T
NM_002796.3(PSMB4):c.693+16G>A
NM_002796.3(PSMB4):c.693+19A>G
NM_002796.3(PSMB4):c.693+8A>G
NM_002796.3(PSMB4):c.694-10T>C
NM_002796.3(PSMB4):c.694-11C>T
NM_002796.3(PSMB4):c.694-12_694-10del
NM_002796.3(PSMB4):c.694-12_694-9del
NM_002796.3(PSMB4):c.694-18T>C
NM_002796.3(PSMB4):c.694-20A>C
NM_002796.3(PSMB4):c.694-20_694-17del	rs1428345745
NM_002796.3(PSMB4):c.694-4C>A	rs148669878
NM_002796.3(PSMB4):c.694-6T>C
NM_002796.3(PSMB4):c.694-7C>T
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.702C>T (p.Ile234=)
NM_002796.3(PSMB4):c.714C>G (p.Thr238=)
NM_002796.3(PSMB4):c.742T>C (p.Leu248=)	rs1652841131
NM_002796.3(PSMB4):c.771C>A (p.Ala257=)
NM_002796.3(PSMB4):c.782+10A>G
NM_002796.3(PSMB4):c.782+11G>A	rs146720393
NM_002796.3(PSMB4):c.782+19A>G	rs1652846273
NM_002796.3(PSMB4):c.782+20T>G
NM_002796.3(PSMB4):c.782+8A>G
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
NM_002796.3(PSMB4):c.786C>T (p.Gly262=)	rs2102124056

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.