CYBRD1[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2382543	NM_024843.4(CYBRD1):c.16T>C (p.Tyr6His)	CYBRD1 (Y6H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2517898	NM_024843.4(CYBRD1):c.173T>G (p.Phe58Cys)	CYBRD1 (F58C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2284997	NM_024843.4(CYBRD1):c.175G>A (p.Val59Ile)	CYBRD1 (V59I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2461006	NM_024843.4(CYBRD1):c.178T>C (p.Phe60Leu)	CYBRD1 (F60L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3079295	NM_024843.4(CYBRD1):c.278C>T (p.Ala93Val)	CYBRD1 (A93V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2220941	NM_024843.4(CYBRD1):c.286C>T (p.Leu96Phe)	CYBRD1 (L38F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3079296	NM_024843.4(CYBRD1):c.292A>G (p.Ile98Val)	CYBRD1 (I98V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2407172	NM_024843.4(CYBRD1):c.343A>G (p.Asn115Asp)	CYBRD1 (N115D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2530941	NM_024843.4(CYBRD1):c.368T>C (p.Val123Ala)	CYBRD1 (V65A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3079297	NM_024843.4(CYBRD1):c.444G>A (p.Pro148=)	CYBRD1 (A79T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2353963	NM_024843.4(CYBRD1):c.527T>C (p.Met176Thr)	CYBRD1 (M176T +1 more)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 2516729	NM_024843.4(CYBRD1):c.528G>A (p.Met176Ile)	CYBRD1 (G107R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079298	NM_024843.4(CYBRD1):c.584C>T (p.Pro195Leu)	CYBRD1 (P195L +1 more)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 2252098	NM_024843.4(CYBRD1):c.638C>A (p.Ala213Asp)	CYBRD1 (A155D +1 more)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 3079299	NM_024843.4(CYBRD1):c.666G>A (p.Pro222=)	CYBRD1 (A153T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 1237711	NM_024843.4(CYBRD1):c.797G>A (p.Ser266Asn)	CYBRD1 (S208N +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign
Select item 3079301	NM_024843.4(CYBRD1):c.848G>A (p.Arg283Lys)	CYBRD1 (R283K +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance