ClinVar Miner

List of variants in gene DNAH8 reported as uncertain significance for not provided

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Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_001206927.2(DNAH8):c.11771C>T (p.Thr3924Met) rs61757218 0.00685
NM_001206927.2(DNAH8):c.10308+107G>A rs371811720 0.00150
NM_001206927.2(DNAH8):c.14059C>T (p.Arg4687Ter) rs146551804 0.00058
NM_001206927.2(DNAH8):c.2150C>G (p.Ser717Cys) rs145798237 0.00055
NM_001206927.2(DNAH8):c.11695C>T (p.Arg3899Trp) rs138030174 0.00052
NM_001206927.2(DNAH8):c.10529A>G (p.Asn3510Ser) rs145843224 0.00040
NM_001206927.2(DNAH8):c.4111G>A (p.Glu1371Lys) rs149020489 0.00039
NM_001206927.2(DNAH8):c.2804A>G (p.His935Arg) rs150379318 0.00038
NM_001206927.2(DNAH8):c.10773C>G (p.Phe3591Leu) rs147574550 0.00031
NM_001206927.2(DNAH8):c.9277A>G (p.Ile3093Val) rs139533720 0.00022
NM_001206927.2(DNAH8):c.725G>A (p.Arg242His) rs142863013 0.00021
NM_001206927.2(DNAH8):c.13417A>C (p.Ile4473Leu) rs200416428 0.00011
NM_001206927.2(DNAH8):c.13282G>C (p.Gly4428Arg) rs755556134 0.00009
NM_001206927.2(DNAH8):c.2285C>T (p.Pro762Leu) rs199804814 0.00008
NM_001206927.2(DNAH8):c.6778G>A (p.Glu2260Lys) rs1018899864 0.00005
NM_001206927.2(DNAH8):c.4083+12T>C rs1202897114 0.00002
NM_001206927.2(DNAH8):c.9197C>T (p.Ser3066Phe) rs1463693356 0.00002
NM_001206927.2(DNAH8):c.10801G>A (p.Asp3601Asn) rs376013784 0.00001
NM_001206927.2(DNAH8):c.2419C>T (p.Arg807Ter) rs567050969 0.00001
NM_001206927.2(DNAH8):c.5654A>G (p.Asn1885Ser) rs1157302965 0.00001
GRCh37/hg19 6p21.2(chr6:38812389-38862242)x3
GRCh37/hg19 6p21.2(chr6:38818643-38884441)x3
NM_001206927.2(DNAH8):c.10447A>T (p.Asn3483Tyr)
NM_001206927.2(DNAH8):c.10760A>G (p.Gln3587Arg) rs373965207
NM_001206927.2(DNAH8):c.11729T>A (p.Phe3910Tyr) rs375158290
NM_001206927.2(DNAH8):c.12100C>T (p.Leu4034Phe) rs146505940
NM_001206927.2(DNAH8):c.12166G>C (p.Asp4056His)
NM_001206927.2(DNAH8):c.12194T>A (p.Ile4065Asn)
NM_001206927.2(DNAH8):c.13701C>G (p.Phe4567Leu)
NM_001206927.2(DNAH8):c.13916C>G (p.Pro4639Arg)
NM_001206927.2(DNAH8):c.3853A>G (p.Met1285Val) rs1773299688
NM_001206927.2(DNAH8):c.6097A>T (p.Thr2033Ser)
NM_001206927.2(DNAH8):c.6548A>G (p.Gln2183Arg)
NM_001206927.2(DNAH8):c.6772G>A (p.Asp2258Asn)
NM_001206927.2(DNAH8):c.9194G>A (p.Arg3065Lys)
NM_001206927.2(DNAH8):c.9514-4A>G
NM_001206927.2(DNAH8):c.9637G>C (p.Asp3213His)

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