ClinVar for Gene (Select 55567) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3272845	NM_001347886.2(DNAH3):c.1939C>A (p.His647Asn)	DNAH3 (H707N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272844	NM_001347886.2(DNAH3):c.8684A>G (p.Asp2895Gly)	DNAH3 (D2895G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272843	NM_001347886.2(DNAH3):c.5419A>G (p.Met1807Val)	DNAH3 (M1853V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272842	NM_001347886.2(DNAH3):c.9528C>G (p.Asn3176Lys)	DNAH3 (N3176K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272841	NM_001347886.2(DNAH3):c.10765C>A (p.Pro3589Thr)	DNAH3 (P3635T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272840	NM_001347886.2(DNAH3):c.7571G>A (p.Gly2524Glu)	DNAH3 (G2524E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272839	NM_001347886.2(DNAH3):c.12061T>G (p.Cys4021Gly)	DNAH3 (C4021G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272838	NM_001347886.2(DNAH3):c.8822A>G (p.Gln2941Arg)	DNAH3 (Q2941R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272837	NM_001347886.2(DNAH3):c.10336A>G (p.Ile3446Val)	DNAH3 (I3492V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272836	NM_001347886.2(DNAH3):c.7478A>G (p.Glu2493Gly)	DNAH3 (E2493G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272835	NM_001347886.2(DNAH3):c.3268G>A (p.Ala1090Thr)	DNAH3 (A1090T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272834	NM_001347886.2(DNAH3):c.6712G>A (p.Gly2238Arg)	DNAH3 (G2238R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272833	NM_001347886.2(DNAH3):c.8204A>G (p.Asp2735Gly)	DNAH3 (D2735G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272832	NM_001347886.2(DNAH3):c.11219A>G (p.Tyr3740Cys)	DNAH3 (Y3740C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272831	NM_001347886.2(DNAH3):c.11260G>A (p.Gly3754Ser)	DNAH3 (G3754S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272830	NM_001347886.2(DNAH3):c.3513T>G (p.Ile1171Met)	DNAH3 (I1217M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272829	NM_001347886.2(DNAH3):c.2423G>A (p.Ser808Asn)	DNAH3 (S808N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272828	NM_001347886.2(DNAH3):c.5129T>C (p.Leu1710Pro)	DNAH3 (L1710P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272827	NM_001347886.2(DNAH3):c.4571T>C (p.Met1524Thr)	DNAH3 (M1524T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272826	NM_001347886.2(DNAH3):c.8545G>A (p.Asp2849Asn)	DNAH3 (D2895N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272825	NM_001347886.2(DNAH3):c.2398G>C (p.Glu800Gln)	DNAH3 (E846Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272824	NM_001347886.2(DNAH3):c.4959G>A (p.Met1653Ile)	DNAH3 (M1699I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272823	NM_001347886.2(DNAH3):c.6925G>A (p.Asp2309Asn)	DNAH3 (D2355N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272822	NM_001347886.2(DNAH3):c.8441G>A (p.Arg2814Gln)	DNAH3 (R2814Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272821	NM_001347886.2(DNAH3):c.4908A>T (p.Lys1636Asn)	DNAH3 (K1636N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272820	NM_001347886.2(DNAH3):c.5986A>G (p.Lys1996Glu)	DNAH3 (K1996E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272819	NM_001347886.2(DNAH3):c.2350A>G (p.Lys784Glu)	DNAH3 (K784E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272818	NM_001347886.2(DNAH3):c.3671T>C (p.Val1224Ala)	DNAH3 (V1224A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272817	NM_001347886.2(DNAH3):c.2506A>G (p.Lys836Glu)	DNAH3 (K836E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272816	NM_001347886.2(DNAH3):c.478A>G (p.Lys160Glu)	DNAH3 (K160E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272815	NM_001347886.2(DNAH3):c.10136G>A (p.Arg3379His)	DNAH3 (R3379H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272814	NM_001347886.2(DNAH3):c.5753C>G (p.Ala1918Gly)	DNAH3 (A1918G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272813	NM_001347886.2(DNAH3):c.3061C>T (p.Arg1021Trp)	DNAH3 (R1021W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272812	NM_001347886.2(DNAH3):c.4255G>A (p.Gly1419Arg)	DNAH3 (G1465R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272811	NM_001347886.2(DNAH3):c.2750T>C (p.Ile917Thr)	DNAH3 (I963T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272810	NM_001347886.2(DNAH3):c.4231G>T (p.Asp1411Tyr)	DNAH3 (D1457Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272808	NM_001347886.2(DNAH3):c.2498T>C (p.Phe833Ser)	DNAH3 (F879S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272807	NM_001347886.2(DNAH3):c.3212A>G (p.Asp1071Gly)	DNAH3 (D1071G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083971	NM_001347886.2(DNAH3):c.9661A>G (p.Lys3221Glu)	DNAH3 (K3267E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083969	NM_001347886.2(DNAH3):c.9025C>A (p.Gln3009Lys)	DNAH3 (Q3009K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083968	NM_001347886.2(DNAH3):c.8849C>G (p.Thr2950Ser)	DNAH3 (T2996S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083967	NM_001347886.2(DNAH3):c.8807C>A (p.Thr2936Asn)	DNAH3 (T2936N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083966	NM_001347886.2(DNAH3):c.8767A>G (p.Lys2923Glu)	DNAH3 (K2969E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083964	NM_001347886.2(DNAH3):c.8665C>T (p.Arg2889Trp)	DNAH3 (R2935W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083963	NM_001347886.2(DNAH3):c.8548C>T (p.Arg2850Cys)	DNAH3 (R2896C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083962	NM_001347886.2(DNAH3):c.8516G>A (p.Cys2839Tyr)	DNAH3 (C2885Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083961	NM_001347886.2(DNAH3):c.8363T>C (p.Leu2788Pro)	DNAH3 (L2834P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083960	NM_001347886.2(DNAH3):c.8230A>G (p.Asn2744Asp)	DNAH3 (N2790D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083959	NM_001347886.2(DNAH3):c.7979A>G (p.Gln2660Arg)	DNAH3 (Q2706R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083958	NM_017539.2(DNAH3):c.79A>T (p.Arg27Trp)	DNAH3, LDAF1 (R27W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3083957	NM_001347886.2(DNAH3):c.7756G>A (p.Val2586Ile)	DNAH3 (V2586I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083955	NM_001347886.2(DNAH3):c.7603C>T (p.Pro2535Ser)	DNAH3 (P2535S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083954	NM_001347886.2(DNAH3):c.7381A>G (p.Met2461Val)	DNAH3 (M2461V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083953	NM_001347886.2(DNAH3):c.7324G>A (p.Val2442Met)	DNAH3 (V2442M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083952	NM_001347886.2(DNAH3):c.649A>G (p.Met217Val)	DNAH3 (M217V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083951	NM_001347886.2(DNAH3):c.7216G>A (p.Ala2406Thr)	DNAH3 (A2406T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3083950	NM_001347886.2(DNAH3):c.7174A>T (p.Ser2392Cys)	DNAH3 (S2392C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083949	NM_001347886.2(DNAH3):c.7062C>G (p.Ser2354Arg)	DNAH3 (S2400R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083948	NM_001347886.2(DNAH3):c.7054A>G (p.Asn2352Asp)	DNAH3 (N2398D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083947	NM_001347886.2(DNAH3):c.6971A>G (p.Glu2324Gly)	DNAH3 (E2324G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083946	NM_001347886.2(DNAH3):c.6967C>T (p.Pro2323Ser)	DNAH3 (P2323S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083945	NM_001347886.2(DNAH3):c.6942C>A (p.Ser2314Arg)	DNAH3 (S2314R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083944	NM_001347886.2(DNAH3):c.599C>T (p.Ser200Leu)	DNAH3 (S200L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3083943	NM_001347886.2(DNAH3):c.6730C>T (p.His2244Tyr)	DNAH3 (H2244Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083942	NM_001347886.2(DNAH3):c.6710A>C (p.Gln2237Pro)	DNAH3 (Q2237P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083941	NM_001347886.2(DNAH3):c.6461C>T (p.Thr2154Ile)	DNAH3 (T2154I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083940	NM_001347886.2(DNAH3):c.6304A>G (p.Lys2102Glu)	DNAH3 (K2102E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083939	NM_001347886.2(DNAH3):c.6070A>G (p.Met2024Val)	DNAH3 (M2024V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3083938	NM_001347886.2(DNAH3):c.6013A>G (p.Met2005Val)	DNAH3 (M2051V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083937	NM_001347886.2(DNAH3):c.5942C>T (p.Thr1981Ile)	DNAH3 (T1981I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083936	NM_001347886.2(DNAH3):c.5762T>A (p.Ile1921Asn)	DNAH3 (I1967N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083935	NM_001347886.2(DNAH3):c.5749G>A (p.Val1917Met)	DNAH3 (V1963M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083934	NM_001347886.2(DNAH3):c.5662G>A (p.Glu1888Lys)	DNAH3 (E1888K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083933	NM_001347886.2(DNAH3):c.5653G>A (p.Val1885Ile)	DNAH3 (V1885I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3083932	NM_017539.2(DNAH3):c.56C>G (p.Pro19Arg)	DNAH3, LDAF1 (P19R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3083931	NM_001347886.2(DNAH3):c.5539C>T (p.Pro1847Ser)	DNAH3 (P1893S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083930	NM_001347886.2(DNAH3):c.5525T>C (p.Met1842Thr)	DNAH3 (M1888T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083929	NM_001347886.2(DNAH3):c.5518A>G (p.Met1840Val)	DNAH3 (M1840V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083928	NM_001347886.2(DNAH3):c.5410A>G (p.Met1804Val)	DNAH3 (M1850V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083927	NM_001347886.2(DNAH3):c.457T>C (p.Ser153Pro)	DNAH3 (S153P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083926	NM_001347886.2(DNAH3):c.5281G>A (p.Val1761Ile)	DNAH3 (V1807I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083925	NM_001347886.2(DNAH3):c.5251G>A (p.Asp1751Asn)	DNAH3 (D1751N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083924	NM_001347886.2(DNAH3):c.5158G>A (p.Glu1720Lys)	DNAH3 (E1720K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083923	NM_001347886.2(DNAH3):c.5145C>A (p.Asp1715Glu)	DNAH3 (D1715E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083922	NM_001347886.2(DNAH3):c.5077T>C (p.Phe1693Leu)	DNAH3 (F1739L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083921	NM_001347886.2(DNAH3):c.4862A>G (p.Tyr1621Cys)	DNAH3 (Y1621C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083920	NM_001347886.2(DNAH3):c.4847T>C (p.Leu1616Pro)	DNAH3 (L1662P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083919	NM_001347886.2(DNAH3):c.4754G>T (p.Arg1585Leu)	DNAH3 (R1585L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083918	NM_001347886.2(DNAH3):c.4718A>G (p.Lys1573Arg)	DNAH3 (K1573R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083917	NM_001347886.2(DNAH3):c.4658A>G (p.Tyr1553Cys)	DNAH3 (Y1599C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083916	NM_001347886.2(DNAH3):c.4382G>A (p.Arg1461Gln)	DNAH3 (R1507Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083914	NM_001347886.2(DNAH3):c.4087G>A (p.Asp1363Asn)	DNAH3 (D1363N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083913	NM_001347886.2(DNAH3):c.4081C>A (p.Leu1361Ile)	DNAH3 (L1361I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083912	NM_001347886.2(DNAH3):c.325C>T (p.Pro109Ser)	DNAH3 (P109S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083910	NM_001347886.2(DNAH3):c.3977G>A (p.Arg1326His)	DNAH3 (R1372H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083909	NM_001347886.2(DNAH3):c.3910G>A (p.Val1304Met)	DNAH3 (V1350M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083908	NM_001347886.2(DNAH3):c.3808G>A (p.Asp1270Asn)	DNAH3 (D1270N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083906	NM_001347886.2(DNAH3):c.3520A>G (p.Met1174Val)	DNAH3 (M1174V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083905	NM_001347886.2(DNAH3):c.3236C>T (p.Ser1079Phe)	DNAH3 (S1079F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083904	NM_001347886.2(DNAH3):c.3017C>G (p.Thr1006Ser)	DNAH3 (T1006S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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