"PreventionGenetics, part of Exact Sciences"[submitter] AND "KIF23"[ge - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 779893	NM_001367805.3(KIF23):c.81+6G>A	KIF23	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 720141	NM_001367805.3(KIF23):c.143A>G (p.Asn48Ser)	KIF23 (N48S)	Single nucleotide variant (5 prime UTR variant +2 more)	KIF23-related disorder +1 more	GBenign/Likely benign
Select item 3054710	NM_001367805.3(KIF23):c.168T>C (p.Thr56=)	KIF23	Single nucleotide variant (5 prime UTR variant +2 more)	KIF23-related disorder	GLikely benign
Select item 2068634	NM_001367805.3(KIF23):c.221C>T (p.Ser74Leu)	KIF23 (S74L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 710300	NM_001367805.3(KIF23):c.230A>G (p.Gln77Arg)	KIF23 (K13E +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 728886	NM_001367805.3(KIF23):c.274G>C (p.Val92Leu)	KIF23 (L27F +1 more)	Single nucleotide variant (missense variant +1 more)	KIF23-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 774916	NM_001367805.3(KIF23):c.293A>G (p.Asn98Ser)	KIF23 (N98S +1 more)	Single nucleotide variant (missense variant +1 more)	KIF23-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 784326	NM_001367805.3(KIF23):c.333T>C (p.Tyr111=)	KIF23	Single nucleotide variant (synonymous variant +2 more)	KIF23-related disorder +1 more	GBenign
Select item 2746272	NM_001367805.3(KIF23):c.798T>A (p.Leu266=)	KIF23	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 1643887	NM_001367805.3(KIF23):c.1115-8dup	KIF23	Duplication (intron variant)	KIF23-related disorder +1 more	GBenign
Select item 2062982	NM_001367805.3(KIF23):c.1115-3C>T	KIF23	Single nucleotide variant (intron variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 732195	NM_001367805.3(KIF23):c.1265G>A (p.Arg422Gln)	KIF23 (R422Q +2 more)	Single nucleotide variant (missense variant +1 more)	KIF23-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 3048864	NM_001367805.3(KIF23):c.1323G>A (p.Met441Ile)	KIF23 (M317I +2 more)	Single nucleotide variant (missense variant +1 more)	KIF23-related disorder	GUncertain significance
Select item 1603408	NM_001367805.3(KIF23):c.1455C>T (p.Asp485=)	KIF23	Single nucleotide variant (synonymous variant +1 more)	KIF23-related disorder +1 more	GLikely benign
Select item 3056833	NM_001367805.3(KIF23):c.2110-10A>C	KIF23	Single nucleotide variant (intron variant)	KIF23-related disorder	GLikely benign
Select item 3057853	NM_001367805.3(KIF23):c.2307A>G (p.Gln769=)	KIF23	Single nucleotide variant (synonymous variant +2 more)	KIF23-related disorder	GLikely benign
Select item 2054804	NM_001367805.3(KIF23):c.2323G>A (p.Val775Met)	KIF23 (V651M +2 more)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GLikely benign
Select item 782006	NM_001367805.3(KIF23):c.2643C>T (p.Ser881=)	KIF23	Single nucleotide variant (synonymous variant +2 more)	not provided +1 more	GBenign/Likely benign
Select item 2186036	NM_001367805.3(KIF23):c.2673+7A>G	KIF23	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 2636408	NM_001367805.3(KIF23):c.2762G>A (p.Arg921Gln)	KIF23 (R713Q +3 more)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GUncertain significance

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Items: 20