Related gene-specific medical variations for Gene (Select 101669766) - ClinVar

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Links from Gene

Items: 37

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3335582	NM_021632.4(ZNF350):c.244T>A (p.Trp82Arg)	ZNF350, ZNF350-AS1 (W82R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335581	NM_021632.4(ZNF350):c.1130G>A (p.Ser377Asn)	ZNF350, ZNF350-AS1 (S377N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335580	NM_021632.4(ZNF350):c.1097G>A (p.Arg366Lys)	ZNF350, ZNF350-AS1 (R366K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335578	NM_021632.4(ZNF350):c.395G>A (p.Arg132His)	ZNF350, ZNF350-AS1 (R132H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3335577	NM_021632.4(ZNF350):c.686C>A (p.Thr229Lys)	ZNF350, ZNF350-AS1 (T229K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335576	NM_021632.4(ZNF350):c.869A>G (p.Tyr290Cys)	ZNF350, ZNF350-AS1 (Y290C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195353	NM_021632.4(ZNF350):c.1586C>G (p.Thr529Arg)	ZNF350, ZNF350-AS1 (T529R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195352	NM_021632.4(ZNF350):c.1456C>T (p.Leu486Phe)	ZNF350, ZNF350-AS1 (L486F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195351	NM_021632.4(ZNF350):c.1322G>A (p.Arg441Lys)	ZNF350, ZNF350-AS1 (R441K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195350	NM_021632.4(ZNF350):c.1084A>G (p.Ile362Val)	ZNF350, ZNF350-AS1 (I362V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2650381	NM_021632.4(ZNF350):c.1179A>C (p.Gln393His)	ZNF350, ZNF350-AS1 (Q393H)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2650380	NM_021632.4(ZNF350):c.1570G>A (p.Val524Ile)	ZNF350, ZNF350-AS1 (V524I)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2616762	NM_021632.4(ZNF350):c.1145C>G (p.Ala382Gly)	ZNF350, ZNF350-AS1 (A382G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599711	NM_021632.4(ZNF350):c.1205A>G (p.Tyr402Cys)	ZNF350, ZNF350-AS1 (Y402C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594696	NM_021632.4(ZNF350):c.644T>A (p.Phe215Tyr)	ZNF350, ZNF350-AS1 (F215Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588441	NM_021632.4(ZNF350):c.1031C>T (p.Thr344Met)	ZNF350, ZNF350-AS1 (T344M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517769	NM_021632.4(ZNF350):c.211G>A (p.Asp71Asn)	ZNF350, ZNF350-AS1 (D71N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512158	NM_021632.4(ZNF350):c.703A>G (p.Arg235Gly)	ZNF350, ZNF350-AS1 (R235G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472797	NM_021632.4(ZNF350):c.596C>T (p.Thr199Ile)	ZNF350, ZNF350-AS1 (T199I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469052	NM_021632.4(ZNF350):c.1450G>A (p.Val484Ile)	ZNF350, ZNF350-AS1 (V484I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2466612	NM_021632.4(ZNF350):c.1144G>A (p.Ala382Thr)	ZNF350, ZNF350-AS1 (A382T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460241	NM_021632.4(ZNF350):c.1213A>G (p.Asn405Asp)	ZNF350, ZNF350-AS1 (N405D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400749	NM_021632.4(ZNF350):c.1227A>C (p.Lys409Asn)	ZNF350, ZNF350-AS1 (K409N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396669	NM_021632.4(ZNF350):c.335T>C (p.Ile112Thr)	ZNF350, ZNF350-AS1 (I112T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395959	NM_021632.4(ZNF350):c.340C>A (p.His114Asn)	ZNF350, ZNF350-AS1 (H114N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391934	NM_021632.4(ZNF350):c.1375G>A (p.Gly459Arg)	ZNF350, ZNF350-AS1 (G459R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375878	NM_021632.4(ZNF350):c.929G>A (p.Arg310Gln)	ZNF350, ZNF350-AS1 (R310Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360768	NM_021632.4(ZNF350):c.827G>A (p.Arg276Gln)	ZNF350, ZNF350-AS1 (R276Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360608	NM_021632.4(ZNF350):c.1438G>A (p.Ala480Thr)	ZNF350, ZNF350-AS1 (A480T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348482	NM_021632.4(ZNF350):c.1328G>C (p.Ser443Thr)	ZNF350, ZNF350-AS1 (S443T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337229	NM_021632.4(ZNF350):c.1016T>G (p.Phe339Cys)	ZNF350, ZNF350-AS1 (F339C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323911	NM_021632.4(ZNF350):c.79G>A (p.Ala27Thr)	ZNF350, ZNF350-AS1 (A27T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309267	NM_021632.4(ZNF350):c.205A>G (p.Ile69Val)	ZNF350, ZNF350-AS1 (I69V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292687	NM_021632.4(ZNF350):c.295A>G (p.Arg99Gly)	ZNF350, ZNF350-AS1 (R99G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232772	NM_021632.4(ZNF350):c.1025G>A (p.Gly342Glu)	ZNF350, ZNF350-AS1 (G342E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231911	NM_021632.4(ZNF350):c.161C>T (p.Pro54Leu)	ZNF350, ZNF350-AS1 (P54L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 712253	NM_021632.4(ZNF350):c.1379C>T (p.Ala460Val)	ZNF350, ZNF350-AS1 (A460V)	Single nucleotide variant (missense variant)	not provided	GBenign

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Links from Gene

Items: 37