"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "NEK9"[g - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 710039	NM_033116.6(NEK9):c.2886A>C (p.Leu962Phe)	NEK9 (L974F +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 726845	NM_033116.6(NEK9):c.2482C>A (p.Pro828Thr)	NEK9 (P828T +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 710224	NM_033116.6(NEK9):c.2442+4A>G	NEK9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 713005	NM_033116.6(NEK9):c.2385A>G (p.Thr795=)	NEK9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 717455	NM_033116.6(NEK9):c.2357G>A (p.Arg786Gln)	NEK9 (R668Q +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 724771	NM_033116.6(NEK9):c.2271C>T (p.Gly757=)	NEK9	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 712149	NM_033116.6(NEK9):c.2232T>C (p.Thr744=)	NEK9	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2138572	NM_033116.6(NEK9):c.1934del (p.Gly645fs)	NEK9 (G645fs +2 more)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2038281	NM_033116.6(NEK9):c.1840+2T>C	NEK9	Single nucleotide variant (splice donor variant)	not provided	GLikely pathogenic
Select item 2060841	NM_033116.6(NEK9):c.1794dup (p.Ile599fs)	NEK9 (I481fs +2 more)	Duplication (frameshift variant)	not provided	GPathogenic
Select item 721955	NM_033116.6(NEK9):c.1236C>T (p.Ala412=)	NEK9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 779690	NM_033116.6(NEK9):c.1050T>C (p.Tyr350=)	NEK9	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2054772	NM_033116.6(NEK9):c.1033C>T (p.Arg345Ter)	NEK9 (R345* +1 more)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 726846	NM_033116.6(NEK9):c.525-12dup	NEK9	Duplication (intron variant)	not provided	GBenign
Select item 715505	NM_033116.6(NEK9):c.486A>G (p.Ser162=)	NEK9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 741729	NM_033116.6(NEK9):c.264G>C (p.Leu88=)	NEK9	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 730012	NM_033116.6(NEK9):c.250G>A (p.Asp84Asn)	NEK9 (D84N)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 734719	NM_033116.6(NEK9):c.222T>C (p.Asp74=)	NEK9	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 768666	NM_033116.6(NEK9):c.128G>C (p.Gly43Ala)	NEK9 (G43A)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 729360	NM_033116.6(NEK9):c.84G>C (p.Ser28=)	NEK9	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 726555	NM_033116.6(NEK9):c.59G>A (p.Ser20Asn)	NEK9 (S20N)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign

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Items: 21