Related gene-specific medical variations for Gene (Select 389333) - ClinVar

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Items: 55

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2655732	NM_001161546.2(PROB1):c.1143G>T (p.Ser381=)	PROB1, SPATA24	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2620762	NM_001161546.2(PROB1):c.477G>C (p.Gln159His)	LOC129994769, PROB1 +1 more (Q159H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2618871	NM_001161546.2(PROB1):c.521G>A (p.Arg174Gln)	LOC129994769, PROB1 +1 more (R174Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2616385	NM_001161546.2(PROB1):c.406A>G (p.Thr136Ala)	PROB1, SPATA24 (T136A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2600639	NM_001161546.2(PROB1):c.376G>A (p.Ala126Thr)	PROB1, SPATA24 (A126T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2569943	NM_001161546.2(PROB1):c.2333C>T (p.Pro778Leu)	LOC129994765, PROB1 +1 more (P778L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2546387	NM_001161546.2(PROB1):c.1061G>C (p.Arg354Pro)	PROB1, SPATA24 (R354P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2538747	NM_001161546.2(PROB1):c.1151C>T (p.Pro384Leu)	PROB1, SPATA24 (P384L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2509725	NM_001161546.2(PROB1):c.2198T>C (p.Ile733Thr)	PROB1, SPATA24 (I733T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2509658	NM_001161546.2(PROB1):c.1283C>T (p.Pro428Leu)	PROB1, SPATA24 (P428L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2493372	NM_001161546.2(PROB1):c.643C>T (p.Arg215Trp)	LOC129994769, PROB1 +1 more (R215W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2484222	NM_001161546.2(PROB1):c.2384G>C (p.Gly795Ala)	LOC129994765, PROB1 +1 more (G795A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2483398	NM_001161546.2(PROB1):c.1940G>A (p.Gly647Glu)	PROB1, SPATA24 (G647E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2481726	NM_001161546.2(PROB1):c.1679C>T (p.Thr560Ile)	LOC129994767, PROB1 +1 more (T560I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2480389	NM_001161546.2(PROB1):c.1346G>A (p.Ser449Asn)	PROB1, SPATA24 (S449N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2473768	NM_001161546.2(PROB1):c.2156G>A (p.Arg719Lys)	PROB1, SPATA24 (R719K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2468227	NM_001161546.2(PROB1):c.836C>A (p.Pro279His)	PROB1, SPATA24 (P279H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2411450	NM_001161546.2(PROB1):c.581A>T (p.Glu194Val)	LOC129994769, PROB1 +1 more (E194V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2403882	NM_001161546.2(PROB1):c.2066C>A (p.Pro689Gln)	PROB1, SPATA24 (P689Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2388063	NM_001161546.2(PROB1):c.827G>A (p.Arg276Gln)	SPATA24, PROB1 (R276Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2385980	NM_001161546.2(PROB1):c.2422G>A (p.Ala808Thr)	LOC129994765, PROB1 +1 more (A808T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2383256	NM_001161546.2(PROB1):c.1399G>A (p.Gly467Arg)	LOC129994768, PROB1 +1 more (G467R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2381142	NM_001161546.2(PROB1):c.583G>A (p.Glu195Lys)	LOC129994769, PROB1 +1 more (E195K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2380608	NM_001161546.2(PROB1):c.2371G>T (p.Val791Leu)	LOC129994765, PROB1 +1 more (V791L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2378744	NM_001161546.2(PROB1):c.1022G>T (p.Ser341Ile)	SPATA24, PROB1 (S341I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2376936	NM_001161546.2(PROB1):c.665C>T (p.Ala222Val)	LOC129994769, PROB1 +1 more (A222V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2375756	NM_001161546.2(PROB1):c.2341G>A (p.Gly781Ser)	LOC129994765, PROB1 +1 more (G781S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2373748	NM_001161546.2(PROB1):c.2080C>T (p.Pro694Ser)	PROB1, SPATA24 (P694S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2351124	NM_001161546.2(PROB1):c.200C>T (p.Ala67Val)	PROB1, SPATA24 (A67V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2334728	NM_001161546.2(PROB1):c.1217G>T (p.Gly406Val)	SPATA24, PROB1 (G406V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2334321	NM_001161546.2(PROB1):c.353G>A (p.Gly118Glu)	SPATA24, PROB1 (G118E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2333193	NM_001161546.2(PROB1):c.466C>G (p.Arg156Gly)	LOC129994769, PROB1 +1 more (R156G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2332824	NM_001161546.2(PROB1):c.2627C>G (p.Ala876Gly)	LOC129994765, PROB1 (A876G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2328129	NM_001161546.2(PROB1):c.1649C>T (p.Thr550Ile)	LOC129994767, PROB1 +1 more (T550I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2309235	NM_001161546.2(PROB1):c.152A>G (p.Lys51Arg)	PROB1, SPATA24 (K51R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2309052	NM_001161546.2(PROB1):c.352G>A (p.Gly118Arg)	PROB1, SPATA24 (G118R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2300528	NM_001161546.2(PROB1):c.1751T>C (p.Val584Ala)	LOC129994767, PROB1 +1 more (V584A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2290944	NM_001161546.2(PROB1):c.961C>G (p.Arg321Gly)	SPATA24, PROB1 (R321G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2285405	NM_001161546.2(PROB1):c.644G>A (p.Arg215Gln)	LOC129994769, PROB1 +1 more (R215Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2284315	NM_001161546.2(PROB1):c.47A>G (p.Gln16Arg)	PROB1, SPATA24 (Q16R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2269240	NM_001161546.2(PROB1):c.919G>A (p.Ala307Thr)	PROB1, SPATA24 (A307T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2261090	NM_001161546.2(PROB1):c.2021C>T (p.Pro674Leu)	SPATA24, PROB1 (P674L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2253653	NM_001161546.2(PROB1):c.29T>C (p.Leu10Pro)	SPATA24, PROB1 (L10P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2226747	NM_001161546.2(PROB1):c.1678A>G (p.Thr560Ala)	LOC129994767, PROB1 +1 more (T560A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2212181	NM_001161546.2(PROB1):c.290G>T (p.Arg97Leu)	PROB1, SPATA24 (R97L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2208981	NM_001161546.2(PROB1):c.2585C>G (p.Ser862Cys)	LOC129994765, PROB1 (S862C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 790451	NM_001161546.2(PROB1):c.32C>T (p.Pro11Leu)	SPATA24, PROB1 (P11L)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 789286	NM_001161546.2(PROB1):c.780C>G (p.Ser260Arg)	PROB1, SPATA24 (S260R)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 785141	NM_001161546.2(PROB1):c.127C>G (p.Pro43Ala)	SPATA24, PROB1 (P43A)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 785140	NM_001161546.2(PROB1):c.1507C>A (p.Pro503Thr)	LOC129994768, PROB1 +1 more (P503T)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 775224	NM_001161546.2(PROB1):c.1475C>G (p.Pro492Arg)	LOC129994768, PROB1 +1 more (P492R)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 734807	NM_001161546.2(PROB1):c.2003C>T (p.Pro668Leu)	PROB1, SPATA24 (P668L)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 712577	NM_001161546.2(PROB1):c.2364C>T (p.Arg788=)	LOC129994765, PROB1 +1 more	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 709228	NM_001161546.2(PROB1):c.1517C>T (p.Ala506Val)	LOC129994768, PROB1 +1 more (A506V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 225701	NM_001161546.2(PROB1):c.671G>A (p.Gly224Asp)	LOC129994769, PROB1 +1 more (G224D)	Single nucleotide variant (missense variant)	Keratoconus 1	GUncertain significance

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Links from Gene

Items: 55