ClinVar Miner

List of variants in gene DNAH8 studied for not provided

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Gene type:
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Total variants: 80
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HGVS dbSNP
GRCh37/hg19 6p21.2(chr6:38812389-38862242)x3
GRCh37/hg19 6p21.2(chr6:38818643-38884441)x3
NM_001206927.2(DNAH8):c.10431C>G (p.Ala3477=) rs1583349041
NM_001206927.2(DNAH8):c.10464G>C (p.Leu3488=) rs1583349134
NM_001206927.2(DNAH8):c.10662+8T>C rs1177385307
NM_001206927.2(DNAH8):c.10674T>C (p.Asn3558=) rs1160474440
NM_001206927.2(DNAH8):c.10773C>G (p.Phe3591Leu) rs147574550
NM_001206927.2(DNAH8):c.1095A>G (p.Val365=) rs142065001
NM_001206927.2(DNAH8):c.10998T>C (p.Asp3666=) rs201841900
NM_001206927.2(DNAH8):c.11457+5TC[6] rs745611444
NM_001206927.2(DNAH8):c.11577T>C (p.Asp3859=) rs369713875
NM_001206927.2(DNAH8):c.11598A>C (p.Val3866=) rs140415898
NM_001206927.2(DNAH8):c.1167A>G (p.Pro389=) rs1254302655
NM_001206927.2(DNAH8):c.11910C>T (p.Tyr3970=) rs372031053
NM_001206927.2(DNAH8):c.12387C>T (p.Cys4129=)
NM_001206927.2(DNAH8):c.12480A>C (p.Gly4160=) rs747928749
NM_001206927.2(DNAH8):c.12562C>T (p.Leu4188=) rs1583484448
NM_001206927.2(DNAH8):c.12583C>T (p.Leu4195=) rs200315521
NM_001206927.2(DNAH8):c.12651T>C (p.His4217=) rs768250990
NM_001206927.2(DNAH8):c.12795G>C (p.Pro4265=) rs188101498
NM_001206927.2(DNAH8):c.12822C>T (p.His4274=) rs1480630966
NM_001206927.2(DNAH8):c.13599G>A (p.Ser4533=) rs150470972
NM_001206927.2(DNAH8):c.14089C>T (p.Leu4697=) rs560936004
NM_001206927.2(DNAH8):c.1548A>G (p.Ala516=) rs146078369
NM_001206927.2(DNAH8):c.210G>A (p.Gly70=) rs1462801040
NM_001206927.2(DNAH8):c.2409G>A (p.Thr803=) rs150073636
NM_001206927.2(DNAH8):c.2419C>T (p.Arg807Ter) rs567050969
NM_001206927.2(DNAH8):c.264T>G (p.Leu88=) rs1582824738
NM_001206927.2(DNAH8):c.2652A>C (p.Pro884=) rs750208062
NM_001206927.2(DNAH8):c.2673T>C (p.Ser891=) rs1583012566
NM_001206927.2(DNAH8):c.2685A>G (p.Gln895=) rs878854273
NM_001206927.2(DNAH8):c.2708C>T (p.Ser903Leu) rs569365870
NM_001206927.2(DNAH8):c.2719C>T (p.Leu907=) rs1060504238
NM_001206927.2(DNAH8):c.2946G>A (p.Lys982=) rs146331687
NM_001206927.2(DNAH8):c.3035-4A>G rs185584533
NM_001206927.2(DNAH8):c.3419A>G (p.His1140Arg) rs377516809
NM_001206927.2(DNAH8):c.3582G>A (p.Ala1194=) rs199802771
NM_001206927.2(DNAH8):c.3822T>C (p.Val1274=) rs1338876432
NM_001206927.2(DNAH8):c.3849G>A (p.Glu1283=) rs878854274
NM_001206927.2(DNAH8):c.3853A>G (p.Met1285Val)
NM_001206927.2(DNAH8):c.4212T>G (p.Val1404=) rs780066300
NM_001206927.2(DNAH8):c.4224A>G (p.Pro1408=) rs778459478
NM_001206927.2(DNAH8):c.4503G>A (p.Leu1501=) rs61757624
NM_001206927.2(DNAH8):c.4512C>T (p.Thr1504=) rs200564814
NM_001206927.2(DNAH8):c.4782T>C (p.Ser1594=) rs1341087912
NM_001206927.2(DNAH8):c.4845+9G>A rs373670534
NM_001206927.2(DNAH8):c.5160C>G (p.Ala1720=) rs200767977
NM_001206927.2(DNAH8):c.5169A>G (p.Val1723=) rs149635351
NM_001206927.2(DNAH8):c.531A>G (p.Glu177=) rs756356607
NM_001206927.2(DNAH8):c.5328T>C (p.His1776=) rs1583179547
NM_001206927.2(DNAH8):c.5331G>A (p.Glu1777=) rs752965059
NM_001206927.2(DNAH8):c.552G>A (p.Ala184=) rs201672902
NM_001206927.2(DNAH8):c.5547A>C (p.Ile1849=) rs776384266
NM_001206927.2(DNAH8):c.5646A>G (p.Ser1882=) rs1583186990
NM_001206927.2(DNAH8):c.5667C>T (p.Ser1889=) rs143295890
NM_001206927.2(DNAH8):c.5727A>G (p.Pro1909=) rs1583187318
NM_001206927.2(DNAH8):c.6273T>C (p.Asp2091=) rs146195264
NM_001206927.2(DNAH8):c.6654C>T (p.Tyr2218=) rs551682867
NM_001206927.2(DNAH8):c.6675A>G (p.Glu2225=) rs1583220331
NM_001206927.2(DNAH8):c.6705C>T (p.Asp2235=) rs1199187878
NM_001206927.2(DNAH8):c.6726G>A (p.Leu2242=) rs878854275
NM_001206927.2(DNAH8):c.6921C>T (p.Asn2307=) rs536642412
NM_001206927.2(DNAH8):c.7281C>A (p.Ile2427=) rs544209258
NM_001206927.2(DNAH8):c.7335T>C (p.Ala2445=) rs144391737
NM_001206927.2(DNAH8):c.7346G>T (p.Arg2449Leu) rs149449115
NM_001206927.2(DNAH8):c.7482A>G (p.Ala2494=) rs375517878
NM_001206927.2(DNAH8):c.7620+15dup rs558170060
NM_001206927.2(DNAH8):c.7728A>G (p.Gly2576=) rs140943630
NM_001206927.2(DNAH8):c.788C>A (p.Ala263Glu) rs145115573
NM_001206927.2(DNAH8):c.8124A>G (p.Pro2708=) rs1583269175
NM_001206927.2(DNAH8):c.816G>A (p.Arg272=) rs1582865584
NM_001206927.2(DNAH8):c.9087G>A (p.Ser3029=) rs201691475
NM_001206927.2(DNAH8):c.9123C>T (p.Ser3041=) rs761783722
NM_001206927.2(DNAH8):c.9126A>G (p.Gly3042=) rs1304105245
NM_001206927.2(DNAH8):c.9277A>G (p.Ile3093Val) rs139533720
NM_001206927.2(DNAH8):c.9285T>C (p.Thr3095=) rs144188084
NM_001206927.2(DNAH8):c.953-8C>T rs1400806860
NM_001206927.2(DNAH8):c.9762G>A (p.Val3254=) rs776814257
NM_001206927.2(DNAH8):c.9972A>C (p.Ala3324=) rs755263773
NM_001206927.2(DNAH8):c.9G>A (p.Lys3=) rs565853864

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