ClinVar for Gene (Select 100134015) - ClinVar

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Links from Gene

Items: 68

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3024835	NM_014948.4(UBOX5):c.1494G>T (p.Pro498=)	UBOX5, UBOX5-AS1 (G497C)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2621804	NM_021826.5(FASTKD5):c.2117A>G (p.Gln706Arg)	FASTKD5, UBOX5 +1 more (Q706R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2614060	NM_021826.5(FASTKD5):c.1757G>A (p.Arg586Gln)	FASTKD5, UBOX5 +1 more (R586Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2612469	NM_021826.5(FASTKD5):c.227C>T (p.Pro76Leu)	FASTKD5, UBOX5 +1 more (P76L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2610745	NM_014948.4(UBOX5):c.1012C>T (p.Pro338Ser)	UBOX5, UBOX5-AS1 (P338S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2598877	NM_021826.5(FASTKD5):c.825T>G (p.Asp275Glu)	FASTKD5, UBOX5 +1 more (D275E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2597951	NM_014948.4(UBOX5):c.1589C>T (p.Pro530Leu)	UBOX5, UBOX5-AS1 (P530L +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2579201	GRCh38/hg38 20p13-11.21(chr20:87153-23635465)x3	ADAM33, ADISSP +731 more	Copy number gain	Renal agenesis	GPathogenic
Select item 2559167	NM_021826.5(FASTKD5):c.2168G>A (p.Arg723Gln)	FASTKD5, UBOX5 +1 more (R723Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2558408	NM_014948.4(UBOX5):c.940C>A (p.Pro314Thr)	UBOX5, UBOX5-AS1 (P314T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2550219	NM_021826.5(FASTKD5):c.269C>T (p.Thr90Ile)	FASTKD5, UBOX5 +1 more (T90I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2547020	NM_021826.5(FASTKD5):c.799A>G (p.Ser267Gly)	FASTKD5, UBOX5 +1 more (S267G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2537992	NM_021826.5(FASTKD5):c.851T>C (p.Leu284Ser)	FASTKD5, UBOX5 +1 more (L284S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2537444	NM_021826.5(FASTKD5):c.1913C>G (p.Ala638Gly)	FASTKD5, UBOX5 +1 more (A638G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2535831	NM_021826.5(FASTKD5):c.197G>A (p.Arg66Gln)	FASTKD5, UBOX5 +1 more (R66Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2523181	NM_021826.5(FASTKD5):c.1258C>T (p.Pro420Ser)	FASTKD5, UBOX5 +1 more (P420S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2480973	NM_014948.4(UBOX5):c.605C>T (p.Ser202Phe)	UBOX5, UBOX5-AS1 (S202F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2476827	NM_021826.5(FASTKD5):c.1277G>A (p.Arg426Gln)	UBOX5, UBOX5-AS1 +1 more (R426Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2470533	NM_014948.4(UBOX5):c.1586G>A (p.Arg529Gln)	UBOX5, UBOX5-AS1 (R475Q +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2468745	NM_014948.4(UBOX5):c.1478A>G (p.Tyr493Cys)	UBOX5, UBOX5-AS1 (Y439C +1 more)	Single nucleotide variant (synonymous variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2466858	NM_014948.4(UBOX5):c.568C>T (p.Arg190Trp)	UBOX5, UBOX5-AS1 (R190W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2460111	NM_021826.5(FASTKD5):c.929T>C (p.Ile310Thr)	UBOX5, UBOX5-AS1 +1 more (I310T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2401375	NM_021826.5(FASTKD5):c.2275G>A (p.Val759Ile)	FASTKD5, UBOX5-AS1 +1 more (V759I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2388657	NM_021826.5(FASTKD5):c.217A>C (p.Ser73Arg)	UBOX5-AS1, FASTKD5 +1 more (S73R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2386087	NM_021826.5(FASTKD5):c.683A>G (p.Tyr228Cys)	FASTKD5, UBOX5-AS1 +1 more (Y228C)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2381826	NM_021826.5(FASTKD5):c.2126A>G (p.Tyr709Cys)	FASTKD5, UBOX5-AS1 +1 more (Y709C)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2379080	NM_014948.4(UBOX5):c.470A>G (p.Gln157Arg)	UBOX5, UBOX5-AS1 (Q157R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2374483	NM_021826.5(FASTKD5):c.1445T>G (p.Leu482Trp)	UBOX5-AS1, UBOX5 +1 more (L482W)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2372599	NM_021826.5(FASTKD5):c.670A>G (p.Met224Val)	UBOX5, FASTKD5 +1 more (M224V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2356196	NM_021826.5(FASTKD5):c.2276T>C (p.Val759Ala)	UBOX5-AS1, FASTKD5 +1 more (V759A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2347650	NM_014948.4(UBOX5):c.569G>A (p.Arg190Gln)	UBOX5, UBOX5-AS1 (R190Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2345625	NM_021826.5(FASTKD5):c.289A>G (p.Arg97Gly)	UBOX5, FASTKD5 +1 more (R97G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2325446	NM_021826.5(FASTKD5):c.77G>C (p.Arg26Pro)	FASTKD5, UBOX5 +1 more (R26P)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2320529	NM_021826.5(FASTKD5):c.1553A>G (p.Asp518Gly)	UBOX5-AS1, FASTKD5 +1 more (D518G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2312318	NM_014948.4(UBOX5):c.963C>A (p.His321Gln)	UBOX5, UBOX5-AS1 (H321Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2311832	NM_014948.4(UBOX5):c.707C>T (p.Pro236Leu)	UBOX5, UBOX5-AS1 (P236L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2301318	NM_021826.5(FASTKD5):c.1091G>A (p.Arg364His)	FASTKD5, UBOX5 +1 more (R364H)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2297497	NM_014948.4(UBOX5):c.1612C>T (p.Arg538Trp)	UBOX5-AS1, UBOX5 (R538W +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2296670	NM_014948.4(UBOX5):c.1391C>A (p.Thr464Asn)	UBOX5, UBOX5-AS1 (T464N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2296298	NM_021826.5(FASTKD5):c.1259C>G (p.Pro420Arg)	FASTKD5, UBOX5 +1 more (P420R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2295146	NM_014948.4(UBOX5):c.1585C>T (p.Arg529Trp)	UBOX5, UBOX5-AS1 (R475W +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2291410	NM_014948.4(UBOX5):c.1052C>T (p.Ala351Val)	UBOX5, UBOX5-AS1 (A351V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2285147	NM_021826.5(FASTKD5):c.1447G>C (p.Glu483Gln)	FASTKD5, UBOX5-AS1 +1 more (E483Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2282055	NM_014948.4(UBOX5):c.947C>G (p.Ser316Cys)	UBOX5, UBOX5-AS1 (S316C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2281288	NM_021826.5(FASTKD5):c.1930G>T (p.Gly644Cys)	UBOX5, FASTKD5 +1 more (G644C)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2268687	NM_021826.5(FASTKD5):c.2095G>T (p.Val699Phe)	FASTKD5, UBOX5 +1 more (V699F)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2263503	NM_021826.5(FASTKD5):c.803A>G (p.Tyr268Cys)	FASTKD5, UBOX5-AS1 +1 more (Y268C)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2263411	NM_014948.4(UBOX5):c.1112A>T (p.His371Leu)	UBOX5-AS1, UBOX5 (H371L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2258876	NM_014948.4(UBOX5):c.394A>C (p.Ser132Arg)	UBOX5-AS1, UBOX5 (S132R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2251094	NM_014948.4(UBOX5):c.1565T>A (p.Met522Lys)	UBOX5-AS1, UBOX5 (M522K +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2249688	NM_014948.4(UBOX5):c.155A>G (p.Tyr52Cys)	UBOX5-AS1, UBOX5 (Y52C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2233385	NM_014948.4(UBOX5):c.1606G>A (p.Val536Met)	UBOX5, UBOX5-AS1 (V536M +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2228416	NM_021826.5(FASTKD5):c.1400A>G (p.Gln467Arg)	FASTKD5, UBOX5 +1 more (Q467R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2224606	NM_021826.5(FASTKD5):c.1202C>T (p.Ser401Leu)	FASTKD5, UBOX5 +1 more (S401L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2206303	NM_021826.5(FASTKD5):c.41G>A (p.Arg14Gln)	UBOX5-AS1, FASTKD5 +1 more (R14Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 155359	GRCh38/hg38 20p13-11.23(chr20:80928-18688031)x3	ADAM33, ADISSP +571 more	Copy number gain	See cases	GPathogenic
Select item 154850	GRCh38/hg38 20p13-12.3(chr20:1269303-8626911)x3	LOC130065331, LOC130065332 +300 more	Copy number gain	See cases	GPathogenic
Select item 154176	GRCh38/hg38 20p13-12.3(chr20:80927-5447679)x3	LOC130065300, LOC130065301 +306 more	Copy number gain	See cases	GUncertain significance
Select item 153731	GRCh38/hg38 20p13-11.1(chr20:80927-26324843)x3	MIR6869, MIR6870 +828 more	Copy number gain	See cases	GPathogenic
Select item 152841	GRCh38/hg38 20p13-12.3(chr20:84402-6159078)x3	ADAM33, ADISSP +347 more	Copy number gain	See cases	GPathogenic
Select item 150785	GRCh38/hg38 20p13-12.3(chr20:80093-6386012)x3	ADAM33, ADISSP +348 more	Copy number gain	See cases	GPathogenic
Select item 149704	GRCh38/hg38 20p13-12.1(chr20:80106-13029401)x3	MCM8, MCM8-AS1 +455 more	Copy number gain	See cases	GPathogenic
Select item 146596	GRCh38/hg38 20p13-q13.33(chr20:99557-64277321)x3	LOC130065566, LOC130065567 +2522 more	Copy number gain	See cases	GPathogenic
Select item 144514	GRCh38/hg38 20p13-q11.1(chr20:80106-30227427)x3	LOC111365169, LOC111365189 +833 more	Copy number gain	See cases	GPathogenic
Select item 59194	GRCh38/hg38 20p13(chr20:3059231-4187716)x3	ADAM33, ADISSP +76 more	Copy number gain	See cases	GPathogenic
Select item 59191	GRCh38/hg38 20p13-11.23(chr20:89939-19071495)x3	LOC130065416, LOC130065417 +579 more	Copy number gain	See cases	GPathogenic
Select item 57514	GRCh38/hg38 20p13-11.21(chr20:89939-25697564)x3	LOC126862999, LOC126863005 +814 more	Copy number gain	See cases	GPathogenic
Select item 57354	GRCh38/hg38 20p13-11.23(chr20:89939-19146279)x3	ADAM33, ADISSP +581 more	Copy number gain	See cases	GPathogenic

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Links from Gene

Items: 68