List of variants in gene HOGA1 reported as uncertain significance by Ambry Genetics

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: 33

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HGVS	dbSNP	gnomAD frequency
NM_138413.4(HOGA1):c.185A>T (p.His62Leu)	rs150812556	0.00030
NM_138413.4(HOGA1):c.299T>C (p.Met100Thr)	rs201630144	0.00019
NM_138413.4(HOGA1):c.106G>A (p.Ala36Thr)	rs573292460	0.00015
NM_138413.4(HOGA1):c.541G>C (p.Asp181His)	rs148621526	0.00012
NM_138413.4(HOGA1):c.934G>A (p.Ala312Thr)	rs115431683	0.00010
NM_138413.4(HOGA1):c.424C>T (p.Arg142Cys)	rs201450556	0.00006
NM_138413.4(HOGA1):c.595G>A (p.Gly199Ser)	rs375436098	0.00005
NM_138413.4(HOGA1):c.668C>T (p.Ser223Leu)	rs142766113	0.00005
NM_138413.4(HOGA1):c.764G>A (p.Arg255Gln)	rs201145417	0.00005
NM_138413.4(HOGA1):c.448C>T (p.Leu150Phe)	rs745919223	0.00004
NM_138413.4(HOGA1):c.349G>A (p.Ala117Thr)	rs370031584	0.00003
NM_138413.4(HOGA1):c.410C>A (p.Thr137Asn)	rs761436139	0.00002
NM_138413.4(HOGA1):c.425G>A (p.Arg142His)	rs368418234	0.00002
NM_138413.4(HOGA1):c.329C>T (p.Ser110Phe)	rs1307213959	0.00001
NM_138413.4(HOGA1):c.33G>T (p.Arg11Ser)	rs778696295	0.00001
NM_138413.4(HOGA1):c.365C>T (p.Thr122Ile)	rs143213321	0.00001
NM_138413.4(HOGA1):c.407T>C (p.Val136Ala)	rs776292240	0.00001
NM_138413.4(HOGA1):c.772T>C (p.Cys258Arg)	rs1236141493	0.00001
NM_138413.4(HOGA1):c.80C>T (p.Ser27Leu)	rs767786474	0.00001
NM_138413.4(HOGA1):c.88G>A (p.Gly30Arg)	rs753970733	0.00001
NM_138413.4(HOGA1):c.154G>A (p.Val52Met)
NM_138413.4(HOGA1):c.182T>C (p.Leu61Pro)
NM_138413.4(HOGA1):c.190C>G (p.Leu64Val)	rs1277676251
NM_138413.4(HOGA1):c.209G>A (p.Arg70Gln)	rs267606763
NM_138413.4(HOGA1):c.266G>T (p.Arg89Leu)	rs765160493
NM_138413.4(HOGA1):c.296C>T (p.Ala99Val)	rs1278794652
NM_138413.4(HOGA1):c.377C>T (p.Ala126Val)	rs781649001
NM_138413.4(HOGA1):c.595G>C (p.Gly199Arg)	rs375436098
NM_138413.4(HOGA1):c.724C>G (p.Leu242Val)
NM_138413.4(HOGA1):c.752G>C (p.Cys251Ser)	rs886047518
NM_138413.4(HOGA1):c.776C>T (p.Thr259Met)	rs144103035
NM_138413.4(HOGA1):c.899G>A (p.Gly300Asp)	rs760180544
NM_138413.4(HOGA1):c.89G>T (p.Gly30Val)	rs759795758

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