List of variants in gene NDUFS2 reported as not provided by MutSpliceDB: a database of splice sites variants effects on splicing, NIH

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001377299.1(NDUFS2):c.1354+5G>A	rs190184430	0.00042
NM_001377299.1(NDUFS2):c.1116G>A (p.Lys372=)
NM_001377299.1(NDUFS2):c.96-2A>G	rs1665273085

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