RNF20[gene] and "single gene"[properties] - ClinVar

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Items: 48

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2208982	NM_019592.7(RNF20):c.38C>T (p.Pro13Leu)	RNF20 (P13L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397500	NM_019592.7(RNF20):c.41G>C (p.Gly14Ala)	RNF20 (G14A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297604	NM_019592.7(RNF20):c.152T>G (p.Leu51Arg)	RNF20 (L51R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155256	NM_019592.7(RNF20):c.222G>C (p.Glu74Asp)	RNF20 (E74D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 135634	NM_019592.7(RNF20):c.247C>T (p.Gln83Ter)	RNF20 (Q83*)	Single nucleotide variant (nonsense)	not provided	Gnot provided
Select item 3155257	NM_019592.7(RNF20):c.305A>G (p.Glu102Gly)	RNF20 (E102G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367356	NM_019592.7(RNF20):c.310A>G (p.Ile104Val)	RNF20 (I104V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345814	NM_019592.7(RNF20):c.544C>T (p.Arg182Cys)	RNF20 (R182C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471204	NM_019592.7(RNF20):c.548G>A (p.Arg183Gln)	RNF20 (R183Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274752	NM_019592.7(RNF20):c.601C>T (p.Leu201Phe)	RNF20 (L201F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155258	NM_019592.7(RNF20):c.647A>C (p.Glu216Ala)	RNF20 (E216A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 743589	NM_019592.7(RNF20):c.676G>A (p.Ala226Thr)	RNF20 (A226T)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2408106	NM_019592.7(RNF20):c.706A>C (p.Thr236Pro)	RNF20 (T236P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155259	NM_019592.7(RNF20):c.730C>T (p.Arg244Cys)	RNF20 (R244C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517861	NM_019592.7(RNF20):c.752C>G (p.Ser251Cys)	RNF20 (S251C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155260	NM_019592.7(RNF20):c.806C>T (p.Ser269Phe)	RNF20 (S269F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155261	NM_019592.7(RNF20):c.883G>T (p.Val295Phe)	RNF20 (V295F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491496	NM_019592.7(RNF20):c.1009G>C (p.Glu337Gln)	RNF20 (E337Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390191	NM_019592.7(RNF20):c.1049G>A (p.Arg350Gln)	RNF20 (R350Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613486	NM_019592.7(RNF20):c.1096G>A (p.Glu366Lys)	RNF20 (E366K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408125	NM_019592.7(RNF20):c.1111G>T (p.Val371Leu)	RNF20 (V371L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468145	NM_019592.7(RNF20):c.1123G>A (p.Val375Ile)	RNF20 (V375I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603991	NM_019592.7(RNF20):c.1304G>C (p.Arg435Thr)	RNF20 (R435T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272928	NM_019592.7(RNF20):c.1331C>T (p.Thr444Ile)	RNF20 (T444I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455008	NM_019592.7(RNF20):c.1528A>G (p.Lys510Glu)	RNF20 (K510E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155253	NM_019592.7(RNF20):c.1577C>T (p.Thr526Ile)	RNF20 (T526I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256294	NM_019592.7(RNF20):c.1586C>T (p.Pro529Leu)	RNF20 (P529L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3314825	NM_019592.7(RNF20):c.1601C>G (p.Ala534Gly)	RNF20 (A534G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545314	NM_019592.7(RNF20):c.1601C>T (p.Ala534Val)	RNF20 (A534V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491153	NM_019592.7(RNF20):c.1604A>G (p.Glu535Gly)	RNF20 (E535G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2566508	NM_019592.7(RNF20):c.1690C>G (p.Arg564Gly)	RNF20 (R564G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373855	NM_019592.7(RNF20):c.1691G>C (p.Arg564Pro)	RNF20 (R564P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365301	NM_019592.7(RNF20):c.1694A>G (p.Asp565Gly)	RNF20 (D565G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2659353	NM_019592.7(RNF20):c.1695T>C (p.Asp565=)	RNF20	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2226809	NM_019592.7(RNF20):c.1856G>A (p.Arg619Gln)	RNF20 (R619Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 780821	NM_019592.7(RNF20):c.1881A>G (p.Lys627=)	RNF20	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3155254	NM_019592.7(RNF20):c.2044A>C (p.Lys682Gln)	RNF20 (K682Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155255	NM_019592.7(RNF20):c.2066A>C (p.Lys689Thr)	RNF20 (K689T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608444	NM_019592.7(RNF20):c.2068A>G (p.Lys690Glu)	RNF20 (K690E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489741	NM_019592.7(RNF20):c.2417A>G (p.Glu806Gly)	RNF20 (E806G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208079	NM_019592.7(RNF20):c.2447T>C (p.Ile816Thr)	RNF20 (I816T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3314828	NM_019592.7(RNF20):c.2462A>G (p.Lys821Arg)	RNF20 (K821R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 716921	NM_019592.7(RNF20):c.2539C>T (p.Leu847Phe)	RNF20 (L847F)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3314827	NM_019592.7(RNF20):c.2555A>T (p.Glu852Val)	RNF20 (E852V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3314826	NM_019592.7(RNF20):c.2612C>T (p.Thr871Ile)	RNF20 (T871I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238724	NM_019592.7(RNF20):c.2642G>A (p.Arg881Gln)	RNF20 (R881Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 750679	NM_019592.7(RNF20):c.2752-9T>C	RNF20	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2302704	NM_019592.7(RNF20):c.2900A>C (p.Asn967Thr)	RNF20 (N967T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 48