Related gene-specific medical variations for Gene (Select 91754) - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2689575	NM_033116.6(NEK9):c.2658_2659inv (p.Pro887Thr)	NEK9 (P769T +2 more)	Inversion (missense variant)	not provided	GUncertain significance
Select item 2432183	NM_033116.6(NEK9):c.664del (p.Leu222fs)	NEK9 (L104fs +1 more)	Deletion (frameshift variant)	not provided	GLikely pathogenic
Select item 2432174	NM_033116.6(NEK9):c.207C>G (p.Tyr69Ter)	NEK9 (Y69*)	Single nucleotide variant (nonsense +1 more)	not provided	GLikely pathogenic
Select item 987460	NM_033116.6(NEK9):c.874-2A>G	NEK9	Single nucleotide variant (splice acceptor variant)	not provided	GLikely pathogenic
Select item 987459	NM_033116.6(NEK9):c.1432del (p.Leu478fs)	NEK9 (L360fs +1 more)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 619170	NM_033116.6(NEK9):c.1505A>G (p.Tyr502Cys)	NEK9 (Y502C +1 more)	Single nucleotide variant (missense variant)	Cleft palate +1 more	GLikely benign
Select item 264672	NM_033116.6(NEK9):c.1715G>T (p.Gly572Val)	NEK9 (G572V +2 more)	Single nucleotide variant (missense variant)	Not Specified	Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant
Select item 264658	NM_033116.6(NEK9):c.1731+1G>T	NEK9	Single nucleotide variant (splice donor variant)	Not Specified	Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant
Select item 161787	NM_033116.6(NEK9):c.1756dup (p.Thr586fs)	NEK9 (T468fs +2 more)	Duplication (frameshift variant)	Malignant tumor of prostate	GUncertain significance