ClinVar Miner

List of variants in gene DNAH1 reported as uncertain significance for not provided

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Gene type:
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Total variants: 55
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HGVS dbSNP gnomAD frequency
NM_015512.5(DNAH1):c.9343C>T (p.Arg3115Trp) rs185397176 0.00109
NM_015512.5(DNAH1):c.10438A>G (p.Ile3480Val) rs143443167 0.00104
NM_015512.5(DNAH1):c.1351A>G (p.Lys451Glu) rs76591348 0.00103
NM_015512.5(DNAH1):c.9814C>T (p.Arg3272Cys) rs200784189 0.00085
NM_015512.5(DNAH1):c.1093G>T (p.Ala365Ser) rs374001771 0.00083
NM_015512.5(DNAH1):c.7742A>G (p.Asn2581Ser) rs200839854 0.00076
NM_015512.5(DNAH1):c.1610G>A (p.Ser537Asn) rs201302159 0.00060
NM_015512.5(DNAH1):c.7109A>C (p.Asp2370Ala) rs202011102 0.00060
NM_015512.5(DNAH1):c.2926G>A (p.Ala976Thr) rs181919231 0.00050
NM_015512.5(DNAH1):c.8885A>C (p.Lys2962Thr) rs199602894 0.00048
NM_015512.5(DNAH1):c.3202G>A (p.Val1068Met) rs201455697 0.00041
NM_015512.5(DNAH1):c.8048G>A (p.Arg2683Gln) rs77451372 0.00035
NM_015512.5(DNAH1):c.7865G>A (p.Arg2622Gln) rs200587980 0.00030
NM_015512.5(DNAH1):c.6412G>A (p.Glu2138Lys) rs375829118 0.00027
NM_015512.5(DNAH1):c.11683A>G (p.Met3895Val) rs376301831 0.00019
NM_015512.5(DNAH1):c.3436A>T (p.Ser1146Cys) rs61734641 0.00009
NM_015512.5(DNAH1):c.374G>A (p.Arg125Gln) rs373203216 0.00009
NM_015512.5(DNAH1):c.10976A>G (p.Asn3659Ser) rs376694884 0.00006
NM_015512.5(DNAH1):c.6293G>A (p.Arg2098His) rs373906923 0.00006
NM_015512.5(DNAH1):c.9893C>T (p.Thr3298Met) rs558196088 0.00006
NM_015512.5(DNAH1):c.12017A>C (p.Gln4006Pro) rs369197857 0.00005
NM_015512.5(DNAH1):c.4457G>A (p.Arg1486Gln) rs540607147 0.00005
NM_015512.5(DNAH1):c.1072C>T (p.Arg358Trp) rs763243743 0.00004
NM_015512.5(DNAH1):c.10958T>C (p.Ile3653Thr) rs780417209 0.00004
NM_015512.5(DNAH1):c.8681A>G (p.Lys2894Arg) rs192608206 0.00003
NM_015512.5(DNAH1):c.10076G>A (p.Gly3359Asp) rs1437972390 0.00001
NM_015512.5(DNAH1):c.1516C>T (p.Arg506Trp) rs532226080 0.00001
NM_015512.5(DNAH1):c.241C>T (p.Pro81Ser) rs770488524 0.00001
NM_015512.5(DNAH1):c.3512C>T (p.Thr1171Ile) rs1363854699 0.00001
NM_015512.5(DNAH1):c.4188C>G (p.Asp1396Glu) rs376317081 0.00001
NM_015512.5(DNAH1):c.548C>T (p.Pro183Leu) rs181177631 0.00001
NM_015512.5(DNAH1):c.5680G>A (p.Glu1894Lys) rs758777068 0.00001
NM_015512.5(DNAH1):c.6701C>T (p.Thr2234Met) rs780434919 0.00001
NM_015512.5(DNAH1):c.6941G>A (p.Arg2314His) rs759815756 0.00001
NM_015512.5(DNAH1):c.11715C>T (p.Asp3905=)
NM_015512.5(DNAH1):c.1204G>A (p.Gly402Ser)
NM_015512.5(DNAH1):c.12089+9C>T
NM_015512.5(DNAH1):c.1252G>A (p.Ala418Thr)
NM_015512.5(DNAH1):c.12784G>A (p.Ala4262Thr)
NM_015512.5(DNAH1):c.1790G>T (p.Arg597Leu)
NM_015512.5(DNAH1):c.3549C>A (p.Asp1183Glu)
NM_015512.5(DNAH1):c.3595G>A (p.Asp1199Asn)
NM_015512.5(DNAH1):c.3598C>T (p.His1200Tyr)
NM_015512.5(DNAH1):c.397A>G (p.Thr133Ala)
NM_015512.5(DNAH1):c.4222A>G (p.Ser1408Gly)
NM_015512.5(DNAH1):c.4799T>C (p.Ile1600Thr)
NM_015512.5(DNAH1):c.5110G>A (p.Val1704Met)
NM_015512.5(DNAH1):c.5272G>A (p.Val1758Met)
NM_015512.5(DNAH1):c.5773G>T (p.Gly1925Trp) rs558171797
NM_015512.5(DNAH1):c.5804C>A (p.Ala1935Asp)
NM_015512.5(DNAH1):c.6211C>T (p.Leu2071Phe)
NM_015512.5(DNAH1):c.643T>A (p.Ser215Thr) rs2153223043
NM_015512.5(DNAH1):c.7147G>T (p.Gly2383Cys)
NM_015512.5(DNAH1):c.7148G>A (p.Gly2383Asp)
NM_015512.5(DNAH1):c.816C>G (p.Asp272Glu)

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