"Athena Diagnostics Inc"[submitter] AND "NDE1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 283526	NM_017668.3(NDE1):c.486C>T (p.Leu162=)	NDE1	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 138430	NM_017668.3(NDE1):c.572C>T (p.Thr191Ile)	NDE1 (T191I)	Single nucleotide variant (missense variant)	NDE1-related condition +3 more	GBenign/Likely benign
Select item 586163	NM_017668.3(NDE1):c.635T>G (p.Val212Gly)	NDE1 (V212G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 30787	NM_017668.3(NDE1):c.684_685del (p.Pro229fs)	NDE1 (P229fs)	Microsatellite (frameshift variant)	not provided +2 more	GPathogenic
Select item 318066	NM_017668.3(NDE1):c.823C>T (p.Arg275Trp)	NDE1 (R275W)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 159022	NM_017668.3(NDE1):c.956C>T (p.Thr319Met)	MYH11, NDE1 (T319M +2 more)	Single nucleotide variant (missense variant)	not specified +4 more	GUncertain significance

ClinVar