WDR76[gene] and "single gene"[properties] - ClinVar

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Items: 40

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2599988	NM_024908.4(WDR76):c.112G>T (p.Ala38Ser)	WDR76 (A38S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2349897	NM_024908.4(WDR76):c.154G>T (p.Ala52Ser)	WDR76 (A52S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3332944	NM_024908.4(WDR76):c.217A>G (p.Lys73Glu)	WDR76 (K9E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332942	NM_024908.4(WDR76):c.246G>C (p.Lys82Asn)	WDR76 (K18N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190253	NM_024908.4(WDR76):c.261G>T (p.Lys87Asn)	WDR76 (K87N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386635	NM_024908.4(WDR76):c.352A>G (p.Thr118Ala)	WDR76 (T118A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545503	NM_024908.4(WDR76):c.509T>C (p.Ile170Thr)	WDR76 (I106T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332945	NM_024908.4(WDR76):c.525C>G (p.Asp175Glu)	WDR76 (D111E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190254	NM_024908.4(WDR76):c.568C>T (p.Arg190Cys)	WDR76 (R190C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190255	NM_024908.4(WDR76):c.652A>G (p.Met218Val)	WDR76 (M154V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253999	NM_024908.4(WDR76):c.685T>A (p.Ser229Thr)	WDR76 (S165T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342509	NM_024908.4(WDR76):c.717A>T (p.Leu239Phe)	WDR76 (L239F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190256	NM_024908.4(WDR76):c.788A>G (p.Asn263Ser)	WDR76 (N263S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2529842	NM_024908.4(WDR76):c.800A>G (p.Lys267Arg)	WDR76 (K203R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482042	NM_024908.4(WDR76):c.802G>C (p.Gly268Arg)	WDR76 (G204R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298763	NM_024908.4(WDR76):c.946A>G (p.Ile316Val)	WDR76 (I252V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2356455	NM_024908.4(WDR76):c.995T>C (p.Val332Ala)	WDR76 (V332A +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2569030	NM_024908.4(WDR76):c.1043C>A (p.Pro348His)	WDR76 (P284H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621700	NM_024908.4(WDR76):c.1115A>G (p.Asn372Ser)	WDR76 (N372S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332946	NM_024908.4(WDR76):c.1157G>A (p.Arg386His)	WDR76 (R386H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190243	NM_024908.4(WDR76):c.1192G>A (p.Val398Met)	WDR76 (V334M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332940	NM_024908.4(WDR76):c.1212T>G (p.Ser404Arg)	WDR76 (S404R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190244	NM_024908.4(WDR76):c.1331C>A (p.Thr444Asn)	WDR76 (T380N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190246	NM_024908.4(WDR76):c.1348A>G (p.Lys450Glu)	WDR76 (K386E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190247	NM_024908.4(WDR76):c.1371C>G (p.His457Gln)	WDR76 (H393Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190248	NM_024908.4(WDR76):c.1576A>G (p.Ser526Gly)	WDR76 (S462G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223097	NM_024908.4(WDR76):c.1600C>T (p.Leu534Phe)	WDR76 (L534F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190249	NM_024908.4(WDR76):c.1637G>A (p.Arg546Gln)	WDR76 (R546Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332943	NM_024908.4(WDR76):c.1655A>G (p.Gln552Arg)	WDR76 (Q552R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458284	NM_024908.4(WDR76):c.1685G>C (p.Cys562Ser)	WDR76 (C498S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513342	NM_024908.4(WDR76):c.1718G>A (p.Arg573Gln)	WDR76 (R509Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280452	NM_024908.4(WDR76):c.1733A>G (p.His578Arg)	WDR76 (H578R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269711	NM_024908.4(WDR76):c.1736A>C (p.Glu579Ala)	WDR76 (E515A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270433	NM_024908.4(WDR76):c.1774C>T (p.Leu592Phe)	WDR76 (L528F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360391	NM_024908.4(WDR76):c.1783G>C (p.Val595Leu)	WDR76 (V531L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592804	NM_024908.4(WDR76):c.1813C>T (p.Arg605Trp)	WDR76 (R605W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521943	NM_024908.4(WDR76):c.1820T>G (p.Ile607Ser)	WDR76 (I543S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329369	NM_024908.4(WDR76):c.1835A>C (p.Asn612Thr)	WDR76 (N612T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190251	NM_024908.4(WDR76):c.1863G>T (p.Met621Ile)	WDR76 (M557I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190252	NM_024908.4(WDR76):c.1868A>G (p.Glu623Gly)	WDR76 (E559G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 40