"Baylor Genetics"[submitter] AND "NDUFA13"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2441769	NM_015965.7(NDUFA13):c.44dup (p.Tyr16fs)	LOC130064074, NDUFA13 (Y16fs)	Duplication (frameshift variant)	Hurthle cell carcinoma of thyroid +1 more	GLikely pathogenic
Select item 2671946	NM_015965.7(NDUFA13):c.94+1G>A	LOC130064074, NDUFA13	Single nucleotide variant (splice donor variant)	Hurthle cell carcinoma of thyroid +1 more	GLikely pathogenic