ClinVar Miner

List of variants in gene DNAH11 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_001277115.2(DNAH11):c.10472G>A (p.Arg3491His) rs370932895 0.00048
NM_001277115.2(DNAH11):c.5132A>G (p.Gln1711Arg) rs189432084 0.00031
NM_001277115.2(DNAH11):c.11804C>T (p.Pro3935Leu) rs72658814 0.00025
NM_001277115.2(DNAH11):c.8072A>G (p.Gln2691Arg) rs183682756 0.00021
NM_001277115.2(DNAH11):c.2824C>A (p.Pro942Thr) rs189569144 0.00018
NM_001277115.2(DNAH11):c.6116C>T (p.Ala2039Val) rs371460473 0.00004
NM_001277115.2(DNAH11):c.6984G>T (p.Pro2328=) rs761918179 0.00003
NM_001277115.2(DNAH11):c.10780C>T (p.Pro3594Ser) rs746317366 0.00001
NM_001277115.2(DNAH11):c.1459C>G (p.Leu487Val) rs759291863 0.00001
NM_001277115.2(DNAH11):c.6376G>A (p.Val2126Met) rs772530809 0.00001
NM_001277115.2(DNAH11):c.10352A>G (p.Glu3451Gly)
NM_001277115.2(DNAH11):c.11812G>A (p.Asp3938Asn) rs1783347554
NM_001277115.2(DNAH11):c.12264C>G (p.His4088Gln) rs368428210
NM_001277115.2(DNAH11):c.13167_13177dup (p.Met4393fs) rs1583827297
NM_001277115.2(DNAH11):c.180C>T (p.Arg60=) rs781089233
NM_001277115.2(DNAH11):c.3476G>A (p.Arg1159Lys) rs1192624503
NM_001277115.2(DNAH11):c.5528A>C (p.His1843Pro) rs1783249574
NM_001277115.2(DNAH11):c.7450G>A (p.Val2484Ile)
NM_001277115.2(DNAH11):c.7915-6T>G rs753233190
NM_001277115.2(DNAH11):c.8567T>A (p.Val2856Asp)

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