CCDC92[gene] and "single gene"[properties] - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2221953	NM_025140.3(CCDC92):c.937G>A (p.Asp313Asn)	CCDC92 (D296N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139642	NM_025140.3(CCDC92):c.916G>A (p.Glu306Lys)	CCDC92 (E289K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613868	NM_025140.3(CCDC92):c.896C>T (p.Thr299Ile)	CCDC92 (T282I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360306	NM_025140.3(CCDC92):c.881G>A (p.Arg294Gln)	CCDC92 (R277Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613655	NM_025140.3(CCDC92):c.869G>C (p.Gly290Ala)	CCDC92 (G273A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615786	NM_025140.3(CCDC92):c.864C>A (p.His288Gln)	CCDC92 (H288Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249331	NM_025140.3(CCDC92):c.820G>A (p.Gly274Ser)	CCDC92 (G257S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3139640	NM_025140.3(CCDC92):c.811G>A (p.Asp271Asn)	CCDC92 (D254N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347127	NM_025140.3(CCDC92):c.805G>A (p.Ala269Thr)	CCDC92 (A252T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139639	NM_025140.3(CCDC92):c.800C>G (p.Pro267Arg)	CCDC92 (P250R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595837	NM_025140.3(CCDC92):c.799C>G (p.Pro267Ala)	CCDC92 (P250A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605590	NM_025140.3(CCDC92):c.790G>A (p.Val264Ile)	CCDC92 (V247I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602553	NM_025140.3(CCDC92):c.760G>A (p.Glu254Lys)	CCDC92 (E254K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468134	NM_025140.3(CCDC92):c.701G>A (p.Arg234Gln)	CCDC92 (R217Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472193	NM_025140.3(CCDC92):c.682A>G (p.Ser228Gly)	CCDC92 (S211G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315921	NM_025140.3(CCDC92):c.677C>T (p.Ala226Val)	CCDC92 (A209V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384599	NM_025140.3(CCDC92):c.608G>A (p.Arg203His)	CCDC92 (R203H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220230	NM_025140.3(CCDC92):c.602C>T (p.Thr201Met)	CCDC92 (T184M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139638	NM_025140.3(CCDC92):c.502A>C (p.Lys168Gln)	CCDC92 (K151Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2622959	NM_025140.3(CCDC92):c.373G>A (p.Glu125Lys)	CCDC92 (E108K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139637	NM_025140.3(CCDC92):c.301G>A (p.Glu101Lys)	CCDC92 (E84K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289575	NM_025140.3(CCDC92):c.255G>T (p.Lys85Asn)	CCDC92 (K85N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139636	NM_025140.3(CCDC92):c.160C>T (p.Arg54Trp)	CCDC92 (R54W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485163	NM_025140.3(CCDC92):c.151G>A (p.Glu51Lys)	CCDC92 (E51K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219634	NM_025140.3(CCDC92):c.116G>A (p.Arg39Gln)	CCDC92 (R22Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139641	NM_025140.3(CCDC92):c.86G>A (p.Ser29Asn)	CCDC92 (S12N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 26