ClinVar Miner

List of variants in gene DNAH11 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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Total variants: 36
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HGVS dbSNP gnomAD frequency
NM_001277115.2(DNAH11):c.4001T>C (p.Ile1334Thr) rs72657309 0.00171
NM_001277115.2(DNAH11):c.11277C>G (p.Ile3759Met) rs202148932 0.00069
NM_001277115.2(DNAH11):c.10472G>A (p.Arg3491His) rs370932895 0.00048
NM_001277115.2(DNAH11):c.7553T>C (p.Val2518Ala) rs141807661 0.00046
NM_001277115.2(DNAH11):c.5519C>T (p.Thr1840Ile) rs374351807 0.00043
NM_001277115.2(DNAH11):c.11804C>T (p.Pro3935Leu) rs72658814 0.00025
NM_001277115.2(DNAH11):c.11249T>G (p.Val3750Gly) rs199864090 0.00024
NM_001277115.2(DNAH11):c.9783G>C (p.Glu3261Asp) rs201944089 0.00022
NM_001277115.2(DNAH11):c.4775G>T (p.Cys1592Phe) rs72657327 0.00021
NM_001277115.2(DNAH11):c.8072A>G (p.Gln2691Arg) rs183682756 0.00021
NM_001277115.2(DNAH11):c.472C>T (p.His158Tyr) rs374186868 0.00020
NM_001277115.2(DNAH11):c.8230C>T (p.Arg2744Cys) rs374826188 0.00016
NM_001277115.2(DNAH11):c.13243A>C (p.Lys4415Gln) rs372325290 0.00011
NM_001277115.2(DNAH11):c.338C>A (p.Ala113Glu) rs772913999 0.00011
NM_001277115.2(DNAH11):c.773T>C (p.Ile258Thr) rs771437656 0.00010
NM_001277115.2(DNAH11):c.1567T>C (p.Tyr523His) rs200126117 0.00009
NM_001277115.2(DNAH11):c.11081A>T (p.Asn3694Ile) rs528354205 0.00008
NM_001277115.2(DNAH11):c.5144G>A (p.Arg1715His) rs763926220 0.00008
NM_001277115.2(DNAH11):c.13175C>T (p.Thr4392Met) rs181603431 0.00007
NM_001277115.2(DNAH11):c.1848G>A (p.Gln616=) rs369146775 0.00007
NM_001277115.2(DNAH11):c.6514G>C (p.Val2172Leu) rs375008007 0.00006
NM_001277115.2(DNAH11):c.991G>A (p.Glu331Lys) rs550602612 0.00006
NM_001277115.2(DNAH11):c.10274C>A (p.Thr3425Lys) rs367800491 0.00004
NM_001277115.2(DNAH11):c.698C>T (p.Pro233Leu) rs776376992 0.00004
NM_001277115.2(DNAH11):c.8552C>G (p.Ala2851Gly) rs766265779 0.00004
NM_001277115.2(DNAH11):c.5155A>G (p.Thr1719Ala) rs369965539 0.00003
NM_001277115.2(DNAH11):c.6295G>A (p.Asp2099Asn) rs750251384 0.00002
NM_001277115.2(DNAH11):c.11087G>A (p.Arg3696Lys) rs1262229619 0.00001
NM_001277115.2(DNAH11):c.11398G>C (p.Asp3800His) rs553943791 0.00001
NM_001277115.2(DNAH11):c.11546G>T (p.Gly3849Val) rs145735492 0.00001
NM_001277115.2(DNAH11):c.13112C>T (p.Pro4371Leu) rs1238638659 0.00001
NM_001277115.2(DNAH11):c.4318G>C (p.Val1440Leu) rs753773546 0.00001
NM_001277115.2(DNAH11):c.5413A>G (p.Ile1805Val) rs776549742 0.00001
NM_001277115.2(DNAH11):c.10091G>T (p.Arg3364Leu) rs369682703
NM_001277115.2(DNAH11):c.10701G>T (p.Arg3567Ser) rs375965591
NM_001277115.2(DNAH11):c.7472G>C (p.Arg2491Pro) rs369438218

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