Related gene-specific medical variations for Gene (Select 55536) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3221484	NM_001277115.2(DNAH11):c.13373C>G (p.Pro4458Arg)	CDCA7L, DNAH11 (P4458R +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GUncertain significance
Select item 3083504	NM_001277115.2(DNAH11):c.13439T>C (p.Val4480Ala)	CDCA7L, DNAH11 (V4480A +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GUncertain significance
Select item 3023621	NM_001277115.2(DNAH11):c.13362A>T (p.Ala4454=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 3010788	NM_001277115.2(DNAH11):c.13506T>G (p.Thr4502=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2992675	NM_001277115.2(DNAH11):c.13320C>T (p.Thr4440=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2969697	NM_018719.5(CDCA7L):c.*1327dup	CDCA7L, DNAH11	Duplication (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GBenign
Select item 2956281	NM_001277115.2(DNAH11):c.13545A>G (p.Glu4515=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2955220	NM_018719.5(CDCA7L):c.1333_1334del	CDCA7L, DNAH11	Deletion (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2920353	NM_001277115.2(DNAH11):c.13449C>A (p.Thr4483=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2919234	NM_001277115.2(DNAH11):c.13380_13383dup (p.Ala4462fs)	CDCA7L, DNAH11 (A4462fs)	Duplication (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GPathogenic
Select item 2917274	NM_018719.5(CDCA7L):c.*1328CA[1]	CDCA7L, DNAH11	Microsatellite (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2910777	NM_001277115.2(DNAH11):c.13457G>A (p.Arg4486Lys)	CDCA7L, DNAH11 (R4493K +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GUncertain significance
Select item 2903702	NM_001277115.2(DNAH11):c.13329A>T (p.Gly4443=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2896590	NM_001277115.2(DNAH11):c.13524T>C (p.Ala4508=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2896572	NM_018719.5(CDCA7L):c.*1330C>T	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2893769	NM_001277115.2(DNAH11):c.13480_13489dup (p.Lys4497fs)	CDCA7L, DNAH11 (K4497fs)	Duplication (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GPathogenic
Select item 2890852	NM_001277115.2(DNAH11):c.13308C>A (p.Ala4436=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2890820	NM_001277115.2(DNAH11):c.13313G>A (p.Trp4438Ter)	CDCA7L, DNAH11 (W4438* +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GPathogenic
Select item 2888264	NM_018719.5(CDCA7L):c.*1320G>A	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2880956	NM_001277115.2(DNAH11):c.13322_13335dup (p.Val4446fs)	CDCA7L, DNAH11 (V4446fs)	Duplication (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GPathogenic
Select item 2858135	NM_001277115.2(DNAH11):c.13539T>G (p.Leu4513=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2853678	NM_001277115.2(DNAH11):c.13398C>A (p.Pro4466=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2848096	NM_001277115.2(DNAH11):c.13446A>G (p.Arg4482=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2840690	NM_001277115.2(DNAH11):c.13416del (p.Lys4473fs)	CDCA7L, DNAH11 (K4473fs)	Deletion (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GPathogenic
Select item 2838485	NM_001277115.2(DNAH11):c.13416_13428del (p.Lys4473fs)	CDCA7L, DNAH11 (K4473fs)	Deletion (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GPathogenic
Select item 2833363	NM_001277115.2(DNAH11):c.13410A>G (p.Gln4470=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2820600	NM_001277115.2(DNAH11):c.13461C>A (p.Gly4487=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2816939	NM_001277115.2(DNAH11):c.13395C>G (p.Thr4465=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2810834	NM_001277115.2(DNAH11):c.13521G>A (p.Leu4507=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2806095	NM_001277115.2(DNAH11):c.13396_13426dup (p.Tyr4476fs)	DNAH11, CDCA7L (Y4476fs)	Duplication (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GPathogenic
Select item 2802655	NM_001277115.2(DNAH11):c.13383T>C (p.Phe4461=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2790076	NM_001277115.2(DNAH11):c.13542A>G (p.Leu4514=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	DNAH11-related disorder +1 more	GLikely benign
Select item 2784625	NM_001277115.2(DNAH11):c.13411_13423del (p.Glu4471fs)	CDCA7L, DNAH11 (E4471fs)	Deletion (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GPathogenic
Select item 2781394	NM_001277115.2(DNAH11):c.13476dup (p.Thr4493fs)	CDCA7L, DNAH11 (T4493fs)	Duplication (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GPathogenic
Select item 2767924	NM_018719.5(CDCA7L):c.*1335G>A	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2759706	NM_001277115.2(DNAH11):c.13439_13449dup (p.Lys4484fs)	CDCA7L, DNAH11 (K4484fs)	Duplication (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GPathogenic
Select item 2759129	NM_001277115.2(DNAH11):c.13467C>T (p.Ser4489=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2758563	NM_001277115.2(DNAH11):c.13409_13424del (p.Gln4470fs)	CDCA7L, DNAH11 (Q4470fs)	Deletion (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GPathogenic
Select item 2746067	NM_018719.5(CDCA7L):c.*1334G>C	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2740723	NM_001277115.2(DNAH11):c.13416C>T (p.Thr4472=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2739591	NM_018719.5(CDCA7L):c.*1334G>T	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2733656	NM_001277115.2(DNAH11):c.13416_13449dup (p.Lys4484delinsGlnThrAspLeuArgValProCysValTer)	CDCA7L, DNAH11	Duplication (3 prime UTR variant +2 more)	Primary ciliary dyskinesia	GPathogenic
Select item 2726681	NM_001277115.2(DNAH11):c.13530G>A (p.Val4510=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2726490	NM_018719.5(CDCA7L):c.*1321G>A	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2724033	NM_001277115.2(DNAH11):c.13420C>T (p.Gln4474Ter)	CDCA7L, DNAH11 (Q4481* +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GPathogenic
Select item 2720779	NM_001277115.2(DNAH11):c.13429_13449dup (p.Thr4483_Lys4484insGluCysProValTyrArgThr)	CDCA7L, DNAH11	Duplication (3 prime UTR variant +2 more)	Primary ciliary dyskinesia	GUncertain significance
Select item 2719000	NM_001277115.2(DNAH11):c.13316A>G (p.Asp4439Gly)	CDCA7L, DNAH11 (D4446G +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GUncertain significance
Select item 2715832	NM_001277115.2(DNAH11):c.13431G>A (p.Glu4477=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2703683	NM_018719.5(CDCA7L):c.*1322C>A	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2697453	NM_001277115.2(DNAH11):c.13406_13409del (p.Arg4469fs)	CDCA7L, DNAH11 (R4469fs)	Microsatellite (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GPathogenic
Select item 2696899	NM_018719.5(CDCA7L):c.*1328C>G	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2694385	NM_001277115.2(DNAH11):c.13323A>G (p.Gln4441=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2662022	NM_001277115.2(DNAH11):c.13321C>G (p.Gln4441Glu)	CDCA7L, DNAH11 (Q4441E +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 2636097	NM_001277115.2(DNAH11):c.13499A>G (p.Glu4500Gly)	CDCA7L, DNAH11 (E4500G +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	DNAH11-related disorder	GUncertain significance
Select item 2500231	NM_001277115.2(DNAH11):c.13523_13524insCTGGAGTGGCTCTGCTTCTAG (p.Ala4508_Gly4509insTrpSerGlySerAlaSerSer)	CDCA7L, DNAH11	Insertion (3 prime UTR variant +2 more)	Primary ciliary dyskinesia 7	GLikely pathogenic
Select item 2496510	NM_001277115.2(DNAH11):c.13537C>A (p.Leu4513Ile)	CDCA7L, DNAH11 (L4520I +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GUncertain significance
Select item 2200363	NM_001277115.2(DNAH11):c.13485G>A (p.Arg4495=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2045856	NM_001277115.2(DNAH11):c.13425C>T (p.Thr4475=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 2041084	NM_001277115.2(DNAH11):c.13319C>T (p.Thr4440Ile)	CDCA7L, DNAH11 (T4440I +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GUncertain significance
Select item 2024972	NM_001277115.2(DNAH11):c.13475_13504dup (p.Lys4501_Thr4502insArgThrPheArgLeuLysSerGluGluLys)	CDCA7L, DNAH11	Duplication (3 prime UTR variant +2 more)	Primary ciliary dyskinesia	GUncertain significance
Select item 2001902	NM_001277115.2(DNAH11):c.13325C>G (p.Ala4442Gly)	CDCA7L, DNAH11 (A4442G +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GUncertain significance
Select item 1984351	NM_018719.5(CDCA7L):c.*1335G>T	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 1971166	NM_001277115.2(DNAH11):c.13420C>G (p.Gln4474Glu)	CDCA7L, DNAH11 (Q4474E +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GUncertain significance
Select item 1944204	NM_001277115.2(DNAH11):c.13320_13350dup (p.Lys4451delinsProSerArgAsnHisCysTer)	CDCA7L, DNAH11	Duplication (3 prime UTR variant +2 more)	Primary ciliary dyskinesia	GPathogenic
Select item 1803252	NM_001277115.2(DNAH11):c.13472_13490dup (p.Lys4497fs)	CDCA7L, DNAH11 (K4497fs)	Duplication (3 prime UTR variant +1 more)	Primary ciliary dyskinesia 7	GLikely pathogenic
Select item 1770446	NM_001277115.2(DNAH11):c.13455G>A (p.Leu4485=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 1770385	NM_001277115.2(DNAH11):c.13428C>T (p.Tyr4476=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 1770208	NM_001277115.2(DNAH11):c.13342G>A (p.Ala4448Thr)	CDCA7L, DNAH11 (A4448T +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GUncertain significance
Select item 1770190	NM_001277115.2(DNAH11):c.13331C>G (p.Thr4444Ser)	CDCA7L, DNAH11 (T4451S +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GUncertain significance
Select item 1678874	NM_001277115.2(DNAH11):c.13346_13367del (p.Arg4449fs)	CDCA7L, DNAH11 (R4449fs)	Deletion (3 prime UTR variant +1 more)	Situs inversus +1 more	GLikely pathogenic
Select item 1584775	NM_018719.5(CDCA7L):c.*1333C>T	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia 7 +1 more	GLikely benign
Select item 1574572	NM_018719.5(CDCA7L):c.*1334G>A	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia +1 more	GLikely benign
Select item 1467325	NM_001277115.2(DNAH11):c.13396C>T (p.Pro4466Ser)	CDCA7L, DNAH11 (P4466S)	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GUncertain significance
Select item 1457437	NM_001277115.2(DNAH11):c.13480_13492dup (p.Ser4498fs)	DNAH11, CDCA7L (S4498fs)	Duplication (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GPathogenic
Select item 1451503	NM_001277115.2(DNAH11):c.13364_13415dup (p.Lys4473fs)	CDCA7L, DNAH11 (K4473fs)	Duplication (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GPathogenic
Select item 1403283	NM_001277115.2(DNAH11):c.13451_13452dup (p.Leu4485fs)	CDCA7L, DNAH11 (L4485fs)	Duplication (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GPathogenic
Select item 1388713	NM_001277115.2(DNAH11):c.13420C>A (p.Gln4474Lys)	CDCA7L, DNAH11 (Q4474K)	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GUncertain significance
Select item 1387283	NM_001277115.2(DNAH11):c.13389A>G (p.Lys4463=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 1251756	NM_018719.5(CDCA7L):c.*1375AAGT[1]	CDCA7L, DNAH11	Microsatellite (3 prime UTR variant +1 more)	not provided	GBenign
Select item 1169715	NM_001277115.2(DNAH11):c.13374G>A (p.Pro4458=)	DNAH11, CDCA7L	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GBenign/Likely benign
Select item 1107500	NM_001277115.2(DNAH11):c.13464C>A (p.Pro4488=)	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign
Select item 1069068	NM_001277115.2(DNAH11):c.13500_13504del (p.Glu4500fs)	CDCA7L, DNAH11 (E4500fs)	Microsatellite (3 prime UTR variant +1 more)	Primary ciliary dyskinesia +1 more	GConflicting classifications of pathogenicity
Select item 1068371	NM_001277115.2(DNAH11):c.13512_13525del (p.Trp4505fs)	CDCA7L, DNAH11 (W4505fs)	Deletion (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely pathogenic
Select item 1046755	NM_001277115.2(DNAH11):c.13328G>A (p.Gly4443Glu)	DNAH11, CDCA7L (G4443E)	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GUncertain significance
Select item 1044210	NM_001277115.2(DNAH11):c.13472_*75dup (p.Ile4491_Ter4517=)	CDCA7L, DNAH11	Duplication (3 prime UTR variant +2 more)	Primary ciliary dyskinesia	GUncertain significance
Select item 1012795	NM_001277115.2(DNAH11):c.13418_13421dup (p.Tyr4476fs)	CDCA7L, DNAH11 (Y4476fs)	Duplication (3 prime UTR variant +1 more)	Primary ciliary dyskinesia +1 more	GPathogenic/Likely pathogenic
Select item 1004394	NM_001277115.2(DNAH11):c.13482C>G (p.Phe4494Leu)	CDCA7L, DNAH11 (F4494L)	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GUncertain significance
Select item 977565	NM_001277115.2(DNAH11):c.13445G>C (p.Arg4482Thr)	DNAH11, CDCA7L (R4482T)	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GUncertain significance
Select item 977532	NM_001277115.2(DNAH11):c.13310G>A (p.Arg4437His)	CDCA7L, DNAH11 (R4437H)	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia 7 +1 more	GUncertain significance
Select item 957148	NM_001277115.2(DNAH11):c.13527_13547dup (p.Val4510_Ala4516dup)	CDCA7L, DNAH11	Duplication (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GUncertain significance
Select item 955033	NM_001277115.2(DNAH11):c.13444A>G (p.Arg4482Gly)	CDCA7L, DNAH11 (R4482G)	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GUncertain significance
Select item 947045	NM_001277115.2(DNAH11):c.13473C>G (p.Ile4491Met)	CDCA7L, DNAH11 (I4491M)	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GUncertain significance
Select item 945626	NM_001277115.2(DNAH11):c.13421_13453del (p.Gln4474_Lys4484del)	CDCA7L, DNAH11	Deletion (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely pathogenic
Select item 936022	NM_001277115.2(DNAH11):c.13320_13416dup (p.Lys4473delinsProSerArgAsnHisCysTer)	CDCA7L, DNAH11	Duplication (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GPathogenic
Select item 916128	NM_018719.5(CDCA7L):c.*1246G>A	CDCA7L, DNAH11 (P4458L)	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia 7 +1 more	GPathogenic/Likely pathogenic
Select item 909901	NM_018719.5(CDCA7L):c.*788T>C	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant)	Primary ciliary dyskinesia 7	GUncertain significance
Select item 909900	NM_018719.5(CDCA7L):c.*805G>A	CDCA7L, DNAH11	Single nucleotide variant (3 prime UTR variant)	Primary ciliary dyskinesia 7	GUncertain significance
Select item 853422	NM_001277115.2(DNAH11):c.13306G>A (p.Ala4436Thr)	DNAH11, CDCA7L (A4436T)	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GPathogenic
Select item 827635	NM_001277115.2(DNAH11):c.13523_13543dup (p.Ala4508_Leu4514dup)	DNAH11, CDCA7L	Duplication (3 prime UTR variant +1 more)	Primary ciliary dyskinesia 7 +1 more	GConflicting classifications of pathogenicity
Select item 705494	NM_001277115.2(DNAH11):c.13482C>T (p.Phe4494=)	DNAH11, CDCA7L	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia	GLikely benign

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