List of variants reported as pathogenic for leukopenia by Revvity Omics, Revvity

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

Total variants: 18

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_006118.4(HAX1):c.91del (p.Glu31fs)	rs764082747	0.00026
NM_152564.5(VPS13B):c.6657+1G>A	rs180177366	0.00010
NM_152564.5(VPS13B):c.6727G>T (p.Glu2243Ter)	rs146960401	0.00006
NM_152564.5(VPS13B):c.2911C>T (p.Arg971Ter)	rs120074152	0.00001
NM_000081.4(LYST):c.10468G>T (p.Gly3490Ter)
NM_000081.4(LYST):c.11002G>T (p.Glu3668Ter)
NM_000081.4(LYST):c.1467del (p.Glu489fs)	rs80338644
NM_000081.4(LYST):c.1897A>T (p.Lys633Ter)
NM_000081.4(LYST):c.3085C>T (p.Gln1029Ter)	rs80338651
NM_000081.4(LYST):c.7645C>T (p.Gln2549Ter)
NM_000081.4(LYST):c.8358+2T>C
NM_000081.4(LYST):c.9377_9389del (p.Gly3126fs)
NM_000116.5(TAFAZZIN):c.153C>A (p.Tyr51Ter)
NM_006118.4(HAX1):c.125dup (p.Ser43fs)	rs745666437
NM_006118.4(HAX1):c.430dup (p.Val144fs)	rs770288337
NM_007259.5(VPS45):c.671C>A (p.Thr224Asn)	rs879255237
NM_152564.5(VPS13B):c.10381_10382del (p.Leu3462fs)	rs180177371
NM_152564.5(VPS13B):c.8496del (p.Ile2833fs)	rs2130813918

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.