DCAF13[gene] and "single gene"[properties] - ClinVar

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Items: 36

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1269047	NC_000008.11:g.103415131A>C	DCAF13	Single nucleotide variant	not provided	GBenign
Select item 2225185	NM_015420.6(DCAF13):c.157G>A (p.Ala53Thr)	DCAF13 (A53T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322321	NM_015420.6(DCAF13):c.193C>T (p.Pro65Ser)	DCAF13 (P65S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 731721	NM_015420.6(DCAF13):c.210C>A (p.Ala70=)	DCAF13	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2360969	NM_015420.6(DCAF13):c.262G>C (p.Glu88Gln)	DCAF13 (E88Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385197	NM_015420.6(DCAF13):c.278A>G (p.Asn93Ser)	DCAF13 (N93S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 723920	NM_015420.6(DCAF13):c.326C>G (p.Ala109Gly)	DCAF13 (A109G)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2305795	NM_015420.6(DCAF13):c.334C>G (p.Arg112Gly)	DCAF13 (R112G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270966	NM_015420.7(DCAF13):c.-12A>G	DCAF13	Single nucleotide variant (5 prime UTR variant)	not specified	GLikely benign
Select item 3080267	NM_015420.7(DCAF13):c.-8C>G	DCAF13	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 3270965	NM_015420.7(DCAF13):c.68G>A (p.Arg23Lys)	DCAF13 (R23K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080268	NM_015420.7(DCAF13):c.73C>T (p.Pro25Ser)	DCAF13 (P25S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080269	NM_015420.7(DCAF13):c.247C>T (p.Leu83Phe)	DCAF13 (L83F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2310733	NM_015420.7(DCAF13):c.248T>G (p.Leu83Arg)	DCAF13 (L83R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2560569	NM_015420.7(DCAF13):c.352C>T (p.Arg118Cys)	DCAF13 (R118C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2290093	NM_015420.7(DCAF13):c.406T>G (p.Trp136Gly)	DCAF13 (W136G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403808	NM_015420.7(DCAF13):c.421C>T (p.Pro141Ser)	DCAF13 (P141S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080270	NM_015420.7(DCAF13):c.529C>G (p.Gln177Glu)	DCAF13 (Q62E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291513	NM_015420.7(DCAF13):c.535G>C (p.Asp179His)	DCAF13 (D179H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270964	NM_015420.7(DCAF13):c.548A>T (p.Glu183Val)	DCAF13 (E183V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410802	NM_015420.7(DCAF13):c.548A>G (p.Glu183Gly)	DCAF13 (E183G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316622	NM_015420.7(DCAF13):c.571T>G (p.Ser191Ala)	DCAF13 (S191A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2658735	NM_015420.7(DCAF13):c.624+15del	DCAF13	Deletion (intron variant)	not provided	GLikely benign
Select item 2517872	NM_015420.7(DCAF13):c.691C>T (p.Pro231Ser)	DCAF13 (P231S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588570	NM_015420.7(DCAF13):c.743C>T (p.Pro248Leu)	DCAF13 (P133L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474259	NM_015420.7(DCAF13):c.763A>G (p.Thr255Ala)	DCAF13 (T140A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355261	NM_015420.7(DCAF13):c.764C>T (p.Thr255Ile)	DCAF13 (T255I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380992	NM_015420.7(DCAF13):c.980A>G (p.His327Arg)	DCAF13 (H327R)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2210601	NM_015420.7(DCAF13):c.1114G>C (p.Asp372His)	DCAF13 (D372H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484469	NM_015420.7(DCAF13):c.1142T>G (p.Phe381Cys)	DCAF13 (F266C +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2508940	NM_015420.7(DCAF13):c.1166G>A (p.Arg389His)	DCAF13 (R274H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270960	NM_015420.7(DCAF13):c.1223G>A (p.Arg408His)	DCAF13 (R293H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270963	NM_015420.7(DCAF13):c.1229T>C (p.Met410Thr)	DCAF13 (M295T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270962	NM_015420.7(DCAF13):c.1234G>A (p.Glu412Lys)	DCAF13 (E297K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080266	NM_015420.7(DCAF13):c.1247G>A (p.Arg416Gln)	DCAF13 (R416Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511475	NM_015420.7(DCAF13):c.1285T>A (p.Ser429Thr)	DCAF13 (S429T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 36