ClinVar Miner

List of variants in gene DNAH8 studied for Spermatogenic failure 46

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Total variants: 49
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HGVS dbSNP gnomAD frequency
NM_001206927.2(DNAH8):c.11771C>T (p.Thr3924Met) rs61757218 0.00667
NM_001206927.2(DNAH8):c.8339T>C (p.Ile2780Thr) rs142328376 0.00453
NM_001206927.2(DNAH8):c.4908G>T (p.Glu1636Asp) rs61757219 0.00440
NM_001206927.2(DNAH8):c.11776T>C (p.Leu3926=) rs148084212 0.00168
NM_001206927.2(DNAH8):c.13823C>T (p.Thr4608Met) rs142438011 0.00168
NM_001206927.2(DNAH8):c.7471A>G (p.Ile2491Val) rs148698911 0.00101
NM_001206927.2(DNAH8):c.7123A>C (p.Asn2375His) rs141532428 0.00092
NM_001206927.2(DNAH8):c.7774C>T (p.Arg2592Trp) rs113332942 0.00064
NM_001206927.2(DNAH8):c.8869C>T (p.Arg2957Cys) rs143707632 0.00059
NM_001206927.2(DNAH8):c.14059C>T (p.Arg4687Ter) rs146551804 0.00056
NM_001206927.2(DNAH8):c.4303-15T>C rs201364154 0.00048
NM_001206927.2(DNAH8):c.9427C>T (p.Arg3143Cys) rs151313083 0.00048
NM_001206927.2(DNAH8):c.11468C>T (p.Ala3823Val) rs185283741 0.00034
NM_001206927.2(DNAH8):c.725G>A (p.Arg242His) rs142863013 0.00021
NM_001206927.2(DNAH8):c.2980A>T (p.Ile994Leu) rs141818413 0.00019
NM_001206927.2(DNAH8):c.11701G>A (p.Ala3901Thr) rs560568324 0.00012
NM_001206927.2(DNAH8):c.13417A>C (p.Ile4473Leu) rs200416428 0.00012
NM_001206927.2(DNAH8):c.3129T>A (p.Asp1043Glu) rs573755164 0.00009
NM_001206927.2(DNAH8):c.6434A>G (p.Gln2145Arg) rs780541458 0.00009
NM_001206927.2(DNAH8):c.9025C>A (p.Leu3009Met) rs199779645 0.00008
NM_001206927.2(DNAH8):c.12721G>A (p.Ala4241Thr) rs369473998 0.00007
NM_001206927.2(DNAH8):c.10817C>T (p.Thr3606Met) rs758157645 0.00006
NM_001206927.2(DNAH8):c.11106A>T (p.Glu3702Asp) rs113496494 0.00005
NM_001206927.2(DNAH8):c.1759G>C (p.Glu587Gln) rs551431678 0.00005
NM_001206927.2(DNAH8):c.3377G>A (p.Arg1126His) rs776311330 0.00005
NM_001206927.2(DNAH8):c.5210G>A (p.Arg1737His) rs568480936 0.00005
NM_001206927.2(DNAH8):c.11345A>C (p.Asn3782Thr) rs150057448 0.00004
NM_001206927.2(DNAH8):c.13082C>T (p.Pro4361Leu) rs770419203 0.00004
NM_001206927.2(DNAH8):c.2664+2T>C rs753831132 0.00003
NM_001206927.2(DNAH8):c.3268C>T (p.Arg1090Ter) rs199969537 0.00003
NM_001206927.2(DNAH8):c.5038A>G (p.Ser1680Gly) rs541531465 0.00003
NM_001206927.2(DNAH8):c.10963-1G>A rs376903331 0.00002
NM_001206927.2(DNAH8):c.5768A>T (p.His1923Leu) rs994955767 0.00002
NM_001206927.2(DNAH8):c.12601A>G (p.Thr4201Ala) rs139379184 0.00001
NM_001206927.2(DNAH8):c.2100T>G (p.Ile700Met) rs758338554 0.00001
NM_001206927.2(DNAH8):c.6689A>G (p.Lys2230Arg) rs1563044711 0.00001
NM_001206927.2(DNAH8):c.11024T>C (p.Ile3675Thr)
NM_001206927.2(DNAH8):c.11396C>T (p.Thr3799Ile)
NM_001206927.2(DNAH8):c.11422C>T (p.Gln3808Ter) rs2533558063
NM_001206927.2(DNAH8):c.12536del (p.Val4179fs)
NM_001206927.2(DNAH8):c.13546A>G (p.Asn4516Asp) rs1218550898
NM_001206927.2(DNAH8):c.2863G>A (p.Gly955Ser)
NM_001206927.2(DNAH8):c.3006A>T (p.Lys1002Asn) rs1268449600
NM_001206927.2(DNAH8):c.3483_3489del (p.Thr1162fs) rs766707325
NM_001206927.2(DNAH8):c.3601A>G (p.Lys1201Glu) rs1772998152
NM_001206927.2(DNAH8):c.665A>G (p.Tyr222Cys) rs753974456
NM_001206927.2(DNAH8):c.6962_6968del (p.His2321fs) rs752692263
NM_001206927.2(DNAH8):c.7480-1G>A rs2533098735
NM_001206927.2(DNAH8):c.8747+4C>T rs201261721

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