"Ambry Genetics"[submitter] AND "NEK6"[gene] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2254188	NM_014397.6(NEK6):c.-29-8974T>A	NEK6 (W8R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3299233	NM_014397.6(NEK6):c.-29-8971G>A	NEK6 (E9K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2548633	NM_014397.6(NEK6):c.-29-8925G>A	NEK6 (R24Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2218000	NM_014397.6(NEK6):c.-29-8925G>T	NEK6 (R24L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2557554	NM_014397.6(NEK6):c.-26G>A	NEK6 (R10H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2205207	NM_014397.6(NEK6):c.29A>G (p.His10Arg)	NEK6 (H10R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256384	NM_014397.6(NEK6):c.37A>T (p.Ser13Cys)	NEK6 (S47C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256385	NM_014397.6(NEK6):c.40T>C (p.Ser14Pro)	NEK6 (S39P +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3192237	NM_014397.6(NEK6):c.48C>A (p.Asn16Lys)	NEK6 (N41K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521391	NM_014397.6(NEK6):c.64G>T (p.Gly22Trp)	NEK6 (G22W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192244	NM_014397.6(NEK6):c.103A>G (p.Thr35Ala)	NEK6 (T53A +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2375933	NM_014397.6(NEK6):c.104C>T (p.Thr35Met)	NEK6 (T35M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237521	NM_014397.6(NEK6):c.142G>A (p.Glu48Lys)	NEK6 (E82K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299232	NM_014397.6(NEK6):c.172G>A (p.Glu58Lys)	NEK6 (E58K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192260	NM_014397.6(NEK6):c.282C>G (p.Ile94Met)	NEK6 (I112M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557273	NM_014397.6(NEK6):c.402C>G (p.Ile134Met)	NEK6 (I152M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389835	NM_014397.6(NEK6):c.434C>T (p.Pro145Leu)	NEK6 (P170L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316750	NM_014397.6(NEK6):c.478G>A (p.Val160Met)	NEK6 (V178M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382790	NM_014397.6(NEK6):c.496C>T (p.Arg166Cys)	NEK6 (R200C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600330	NM_014397.6(NEK6):c.694T>G (p.Ser232Ala)	NEK6 (S232A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192289	NM_014397.6(NEK6):c.756G>A (p.Met252Ile)	NEK6 (M277I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511905	NM_014397.6(NEK6):c.811G>A (p.Gly271Arg)	NEK6 (G296R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390869	NM_014397.6(NEK6):c.826G>A (p.Glu276Lys)	NEK6 (E294K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343484	NM_014397.6(NEK6):c.895G>A (p.Val299Met)	NEK6 (V299M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2496183	NM_014397.6(NEK6):c.920A>G (p.His307Arg)	NEK6 (H341R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 25