"Ambry Genetics"[submitter] AND "MICAL1"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2401538	NM_022765.4(MICAL1):c.3171C>G (p.Ser1057Arg)	MICAL1 (S1057R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240939	NM_022765.4(MICAL1):c.3140T>A (p.Leu1047His)	MICAL1 (L1066H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1670124	NM_022765.4(MICAL1):c.3120G>T (p.Leu1040Phe)	MICAL1 (L1040F +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2180305	NM_022765.4(MICAL1):c.3050G>A (p.Arg1017Gln)	MICAL1 (R1017Q +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2165538	NM_022765.4(MICAL1):c.3049C>T (p.Arg1017Trp)	MICAL1 (R1017W +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1412266	NM_022765.4(MICAL1):c.3045G>A (p.Met1015Ile)	MICAL1 (M1015I +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1983813	NM_022765.4(MICAL1):c.3035G>A (p.Arg1012Gln)	MICAL1 (R1031Q +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2292557	NM_022765.4(MICAL1):c.3019C>G (p.Leu1007Val)	MICAL1 (L1007V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276175	NM_022765.4(MICAL1):c.2939A>G (p.Lys980Arg)	MICAL1 (K894R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2161593	NM_022765.4(MICAL1):c.2938A>C (p.Lys980Gln)	MICAL1 (K999Q +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2060649	NM_022765.4(MICAL1):c.2873G>A (p.Arg958His)	MICAL1 (R958H +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2299694	NM_022765.4(MICAL1):c.2848G>A (p.Val950Met)	MICAL1 (V864M +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2470268	NM_022765.4(MICAL1):c.2780A>G (p.Lys927Arg)	MICAL1 (K927R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2175092	NM_022765.4(MICAL1):c.2744G>A (p.Arg915His)	MICAL1 (R934H +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1907560	NM_022765.4(MICAL1):c.2675C>T (p.Ala892Val)	MICAL1 (A892V +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2320489	NM_022765.4(MICAL1):c.2651C>T (p.Pro884Leu)	MICAL1 (P903L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2063410	NM_022765.4(MICAL1):c.2621T>C (p.Phe874Ser)	MICAL1 (F874S +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2167401	NM_022765.4(MICAL1):c.2556G>C (p.Trp852Cys)	MICAL1 (W766C +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2074281	NM_022765.4(MICAL1):c.2530G>A (p.Ala844Thr)	MICAL1 (A844T +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2078452	NM_022765.4(MICAL1):c.2474C>A (p.Pro825Gln)	MICAL1 (P825Q +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1543052	NM_022765.4(MICAL1):c.2474C>T (p.Pro825Leu)	MICAL1 (P739L +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1446885	NM_022765.4(MICAL1):c.2458A>G (p.Asn820Asp)	MICAL1 (N839D +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2081265	NM_022765.4(MICAL1):c.2443C>T (p.Arg815Trp)	MICAL1 (R729W +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1402150	NM_022765.4(MICAL1):c.2438G>A (p.Arg813His)	MICAL1 (R813H +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1895633	NM_022765.4(MICAL1):c.2432C>T (p.Pro811Leu)	MICAL1 (P830L +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3126128	NM_022765.4(MICAL1):c.2425T>C (p.Ser809Pro)	MICAL1 (S723P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1528414	NM_022765.4(MICAL1):c.2420G>A (p.Arg807His)	MICAL1 (R721H +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 1376082	NM_022765.4(MICAL1):c.2408G>A (p.Arg803His)	MICAL1 (R803H +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3126127	NM_022765.4(MICAL1):c.2374G>A (p.Ala792Thr)	MICAL1 (A811T +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2276611	NM_022765.4(MICAL1):c.2360C>T (p.Ala787Val)	MICAL1 (A701V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485664	NM_022765.4(MICAL1):c.2309T>G (p.Leu770Arg)	MICAL1 (L789R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1964104	NM_022765.4(MICAL1):c.2237A>G (p.Tyr746Cys)	MICAL1 (Y660C +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1989463	NM_022765.4(MICAL1):c.2197C>T (p.Pro733Ser)	MICAL1 (P647S +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3126125	NM_022765.4(MICAL1):c.2168G>T (p.Arg723Leu)	MICAL1 (R742L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1507247	NM_022765.4(MICAL1):c.2168G>A (p.Arg723His)	MICAL1 (R723H +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2071785	NM_022765.4(MICAL1):c.2150T>G (p.Phe717Cys)	MICAL1 (F631C +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2071303	NM_022765.4(MICAL1):c.2116G>A (p.Val706Ile)	MICAL1 (V706I +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 1494297	NM_022765.4(MICAL1):c.2074G>A (p.Gly692Ser)	MICAL1 (G692S +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1347656	NM_022765.4(MICAL1):c.2045T>C (p.Leu682Pro)	MICAL1 (L596P +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1514176	NM_022765.4(MICAL1):c.2027C>T (p.Pro676Leu)	MICAL1 (P676L +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2343593	NM_022765.4(MICAL1):c.2020C>A (p.Pro674Thr)	MICAL1 (P588T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2161318	NM_022765.4(MICAL1):c.2003C>G (p.Pro668Arg)	MICAL1 (P687R +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2367302	NM_022765.4(MICAL1):c.1922C>A (p.Thr641Asn)	MICAL1 (T660N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2995263	NM_022765.4(MICAL1):c.1895T>A (p.Val632Glu)	MICAL1 (V651E +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2194260	NM_022765.4(MICAL1):c.1894G>A (p.Val632Ile)	MICAL1 (V632I +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2543588	NM_022765.4(MICAL1):c.1890T>G (p.Ser630Arg)	MICAL1 (S630R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2076834	NM_022765.4(MICAL1):c.1783A>G (p.Ser595Gly)	MICAL1 (S509G +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3126123	NM_022765.4(MICAL1):c.1727C>T (p.Ala576Val)	MICAL1 (A490V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603977	NM_022765.4(MICAL1):c.1714G>A (p.Ala572Thr)	MICAL1 (A572T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126122	NM_022765.4(MICAL1):c.1634C>A (p.Ala545Asp)	MICAL1 (A459D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1412525	NM_022765.4(MICAL1):c.1621C>G (p.Leu541Val)	MICAL1 (L541V +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1989922	NM_022765.4(MICAL1):c.1612G>T (p.Ala538Ser)	MICAL1 (A452S +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2040646	NM_022765.4(MICAL1):c.1594G>A (p.Asp532Asn)	MICAL1 (D446N +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2480100	NM_022765.4(MICAL1):c.1577C>T (p.Pro526Leu)	MICAL1 (P545L +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1959668	NM_022765.4(MICAL1):c.1549T>C (p.Trp517Arg)	MICAL1 (W431R +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1992000	NM_022765.4(MICAL1):c.1490A>G (p.Lys497Arg)	MICAL1 (K516R +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2073753	NM_022765.4(MICAL1):c.1486G>A (p.Asp496Asn)	MICAL1 (D410N +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2603911	NM_022765.4(MICAL1):c.1478G>A (p.Arg493Lys)	MICAL1 (R512K +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2324665	NM_022765.4(MICAL1):c.1426C>T (p.Pro476Ser)	MICAL1 (P390S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257956	NM_022765.4(MICAL1):c.1360A>C (p.Asn454His)	MICAL1 (N368H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2190435	NM_022765.4(MICAL1):c.1358G>A (p.Arg453His)	MICAL1 (R367H +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3000385	NM_022765.4(MICAL1):c.1295T>C (p.Val432Ala)	MICAL1 (V432A +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3126120	NM_022765.4(MICAL1):c.1277G>A (p.Gly426Asp)	MICAL1 (G426D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1432978	NM_022765.4(MICAL1):c.1265G>A (p.Arg422Gln)	MICAL1 (R336Q +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1428007	NM_022765.4(MICAL1):c.1234G>A (p.Ala412Thr)	MICAL1 (A326T +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2317272	NM_022765.4(MICAL1):c.1232T>C (p.Leu411Pro)	MICAL1 (L430P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1390948	NM_022765.4(MICAL1):c.1223G>A (p.Arg408Gln)	MICAL1 (R322Q +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3126119	NM_022765.4(MICAL1):c.1136A>C (p.Gln379Pro)	MICAL1 (Q379P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1380870	NM_022765.4(MICAL1):c.1115C>T (p.Ala372Val)	MICAL1 (A391V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 2214574	NM_022765.4(MICAL1):c.1080T>A (p.Asp360Glu)	MICAL1 (D379E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2608349	NM_022765.4(MICAL1):c.1031G>T (p.Gly344Val)	MICAL1 (G363V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2608348	NM_022765.4(MICAL1):c.1030G>T (p.Gly344Cys)	MICAL1 (G344C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1430080	NM_022765.4(MICAL1):c.950A>G (p.Asn317Ser)	MICAL1 (N317S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1984980	NM_022765.4(MICAL1):c.929G>A (p.Arg310His)	MICAL1 (R329H +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2539889	NM_022765.4(MICAL1):c.922G>C (p.Val308Leu)	MICAL1 (V327L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289504	NM_022765.4(MICAL1):c.836T>C (p.Ile279Thr)	MICAL1 (I279T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126132	NM_022765.4(MICAL1):c.781G>A (p.Val261Ile)	MICAL1 (V261I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2193301	NM_022765.4(MICAL1):c.766C>T (p.Pro256Ser)	MICAL1 (P256S +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2074306	NM_022765.4(MICAL1):c.743G>A (p.Arg248His)	MICAL1 (R267H +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2255246	NM_022765.4(MICAL1):c.713T>C (p.Ile238Thr)	MICAL1 (I238T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1508707	NM_022765.4(MICAL1):c.637G>A (p.Val213Ile)	MICAL1 (V213I +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2293922	NM_022765.4(MICAL1):c.602A>G (p.Asn201Ser)	MICAL1 (N201S +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3126131	NM_022765.4(MICAL1):c.586G>A (p.Ala196Thr)	MICAL1 (A215T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1920756	NM_022765.4(MICAL1):c.502G>A (p.Ala168Thr)	MICAL1 (A187T +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3126130	NM_022765.4(MICAL1):c.498G>C (p.Lys166Asn)	MICAL1 (K166N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1916399	NM_022765.4(MICAL1):c.485T>C (p.Leu162Pro)	MICAL1 (L181P +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1905615	NM_022765.4(MICAL1):c.400G>A (p.Asp134Asn)	MICAL1 (D134N +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2144754	NM_022765.4(MICAL1):c.326G>A (p.Arg109Gln)	MICAL1 (R128Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1617253	NM_022765.4(MICAL1):c.322G>A (p.Ala108Thr)	MICAL1 (A108T +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 1385513	NM_022765.4(MICAL1):c.298G>A (p.Ala100Thr)	MICAL1 (A119T +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2074553	NM_022765.4(MICAL1):c.293G>A (p.Arg98Gln)	MICAL1 (R117Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2314974	NM_022765.4(MICAL1):c.242C>T (p.Ala81Val)	MICAL1 (A81V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2064414	NM_022765.4(MICAL1):c.209G>C (p.Arg70Pro)	MICAL1 (R70P +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2211261	NM_022765.4(MICAL1):c.174G>T (p.Trp58Cys)	MICAL1 (W58C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1423725	NM_022765.4(MICAL1):c.169T>C (p.Tyr57His)	MICAL1 (Y76H +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1903056	NM_022765.4(MICAL1):c.127G>C (p.Gly43Arg)	MICAL1 (G43R +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1507171	NM_022765.4(MICAL1):c.71A>G (p.Gln24Arg)	MICAL1 (Q24R +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2280180	NM_022765.4(MICAL1):c.33T>G (p.His11Gln)	MICAL1 (H11Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1350117	NM_022765.4(MICAL1):c.29C>T (p.Ala10Val)	MICAL1 (A10V +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2322800	NM_022765.4(MICAL1):c.8C>T (p.Ser3Leu)	MICAL1 (S3L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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