List of variants in gene ALG8 reported as uncertain significance by Fulgent Genetics, Fulgent 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_024079.5(ALG8):c.1507A>G (p.Ile503Val)	rs17856033	0.00041
NM_024079.5(ALG8):c.1285A>G (p.Ile429Val)	rs200068321	0.00023
NM_024079.5(ALG8):c.1349+5T>C	rs886048685	0.00007
NM_024079.5(ALG8):c.-7C>T	rs542407081	0.00006
NM_024079.5(ALG8):c.337A>G (p.Met113Val)	rs140499974	0.00004
NM_024079.5(ALG8):c.898G>A (p.Gly300Ser)	rs758154434	0.00004
NM_024079.5(ALG8):c.1117T>C (p.Ser373Pro)	rs558379335	0.00003
NM_024079.5(ALG8):c.897C>T (p.Ile299=)	rs886048686	0.00002
NM_024079.5(ALG8):c.1460A>G (p.Tyr487Cys)	rs777557874	0.00001
NM_024079.5(ALG8):c.382A>G (p.Ile128Val)	rs111831728	0.00001
NM_024079.5(ALG8):c.1293C>G (p.Ile431Met)	rs376704970
NM_024079.5(ALG8):c.772G>A (p.Ala258Thr)	rs1860433537
NM_024079.5(ALG8):c.830_831delinsCA (p.Cys277Ser)	rs1565349263

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