ClinVar Miner

List of variants in gene DNAH9 reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_001372.4(DNAH9):c.8414G>A (p.Arg2805His) rs61740362 0.00407
NM_001372.4(DNAH9):c.8715C>T (p.Ile2905=) rs62060898 0.00339
NM_001372.4(DNAH9):c.11921A>T (p.Lys3974Met) rs111574749 0.00292
NM_001372.4(DNAH9):c.9066C>T (p.Val3022=) rs34595876 0.00272
NM_001372.4(DNAH9):c.6810C>T (p.His2270=) rs61732585 0.00267
NM_001372.4(DNAH9):c.1796C>T (p.Pro599Leu) rs141077864 0.00212
NM_001372.4(DNAH9):c.6297C>T (p.Pro2099=) rs143732515 0.00189
NM_001372.4(DNAH9):c.12640G>T (p.Gly4214Cys) rs144547132 0.00180
NM_001372.4(DNAH9):c.2013A>G (p.Ser671=) rs141159135 0.00120
NM_001372.4(DNAH9):c.4377C>T (p.Val1459=) rs145085168 0.00118
NM_001372.4(DNAH9):c.11835G>A (p.Ala3945=) rs144422539 0.00029
NM_001372.4(DNAH9):c.1010C>T (p.Pro337Leu) rs3744574 0.00026
NM_001372.4(DNAH9):c.10095C>T (p.Ala3365=) rs147795678 0.00021
NM_001372.4(DNAH9):c.6525C>T (p.Pro2175=) rs370820383 0.00015
NM_001372.4(DNAH9):c.1181T>G (p.Leu394Arg) rs772254293 0.00004
NM_001372.4(DNAH9):c.5561T>G (p.Ile1854Ser) rs148417462 0.00004
NM_001372.4(DNAH9):c.5651G>C (p.Gly1884Ala) rs577054880 0.00003
NM_001372.4(DNAH9):c.105C>G (p.Ser35Arg)
NM_001372.4(DNAH9):c.11419A>G (p.Met3807Val)
NM_001372.4(DNAH9):c.11570T>C (p.Met3857Thr)
NM_001372.4(DNAH9):c.12218A>C (p.Asn4073Thr)
NM_001372.4(DNAH9):c.1342G>C (p.Val448Leu)
NM_001372.4(DNAH9):c.1667G>A (p.Arg556Lys)
NM_001372.4(DNAH9):c.2525G>A (p.Arg842Gln)
NM_001372.4(DNAH9):c.308dup (p.Leu104fs) rs769795916
NM_001372.4(DNAH9):c.3428A>T (p.Gln1143Leu)
NM_001372.4(DNAH9):c.3464T>C (p.Val1155Ala)
NM_001372.4(DNAH9):c.3601A>G (p.Ile1201Val)
NM_001372.4(DNAH9):c.3744-4G>A
NM_001372.4(DNAH9):c.3828T>G (p.Ser1276=)
NM_001372.4(DNAH9):c.4149G>A (p.Glu1383=)
NM_001372.4(DNAH9):c.4195A>G (p.Met1399Val)
NM_001372.4(DNAH9):c.6430C>T (p.Arg2144Trp)
NM_001372.4(DNAH9):c.674G>C (p.Ser225Thr)
NM_001372.4(DNAH9):c.8349G>A (p.Glu2783=)
NM_001372.4(DNAH9):c.8515G>A (p.Ala2839Thr)
NM_001372.4(DNAH9):c.8883G>A (p.Lys2961=)
NM_001372.4(DNAH9):c.9552C>T (p.Ala3184=)
NM_001372.4(DNAH9):c.9567C>T (p.Ser3189=)
NM_001372.4(DNAH9):c.9572C>T (p.Ala3191Val)

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