"Ambry Genetics"[submitter] AND "CDC16"[gene] - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2361152	NM_001078645.3(CDC16):c.10G>A (p.Glu4Lys)	CDC16, LOC130010209 (E4K)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2400136	NM_001078645.3(CDC16):c.100C>G (p.Arg34Gly)	CDC16 (R34G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2254842	NM_001078645.3(CDC16):c.131C>G (p.Ala44Gly)	CDC16 (A44G +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2624394	NM_001078645.3(CDC16):c.151G>A (p.Ala51Thr)	CDC16 (A50T +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2339470	NM_001078645.3(CDC16):c.169G>A (p.Ala57Thr)	CDC16 (A57T +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2241965	NM_001078645.3(CDC16):c.255G>T (p.Glu85Asp)	CDC16 (E84D +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2555566	NM_001078645.3(CDC16):c.392C>G (p.Ser131Cys)	CDC16 (S131C +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2298102	NM_001078645.3(CDC16):c.394A>G (p.Ile132Val)	CDC16 (I132V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2390813	NM_001078645.3(CDC16):c.413A>G (p.Lys138Arg)	CDC16 (K137R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2512656	NM_001078645.3(CDC16):c.424G>A (p.Ala142Thr)	CDC16 (A142T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2531571	NM_001078645.3(CDC16):c.575A>G (p.Lys192Arg)	CDC16 (K191R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2518046	NM_001078645.3(CDC16):c.594G>T (p.Gln198His)	CDC16 (Q197H +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2294108	NM_001078645.3(CDC16):c.685G>A (p.Glu229Lys)	CDC16 (E229K +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2395189	NM_001078645.3(CDC16):c.700G>A (p.Val234Ile)	CDC16 (V234I +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2516200	NM_001078645.3(CDC16):c.728A>G (p.Tyr243Cys)	CDC16 (Y242C +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2588770	NM_001078645.3(CDC16):c.773T>C (p.Met258Thr)	CDC16 (M164T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2262548	NM_001078645.3(CDC16):c.835A>C (p.Asn279His)	CDC16 (N278H +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2380520	NM_001078645.3(CDC16):c.942T>G (p.His314Gln)	CDC16 (H220Q +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2226763	NM_001078645.3(CDC16):c.998A>G (p.Tyr333Cys)	CDC16 (Y239C +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2357047	NM_001078645.3(CDC16):c.1070A>T (p.Tyr357Phe)	CDC16 (Y263F +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2239438	NM_001078645.3(CDC16):c.1285T>G (p.Leu429Val)	CDC16 (L335V +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2262332	NM_001078645.3(CDC16):c.1463T>A (p.Ile488Asn)	CDC16 (I436N +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2340865	NM_001078645.3(CDC16):c.1730A>G (p.Glu577Gly)	CDC16 (E525G +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2238094	NM_001078645.3(CDC16):c.1733C>T (p.Thr578Met)	CDC16 (T526M +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2492291	NM_001078645.3(CDC16):c.1766C>T (p.Thr589Ile)	CDC16 (T495I +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2261815	NM_001078645.3(CDC16):c.1838C>T (p.Thr613Ile)	CDC16 (T613I +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2378955	NM_001078645.3(CDC16):c.1859C>T (p.Thr620Met)	CDC16 (T620M +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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Items: 27