ClinVar Miner

List of variants in gene DNAH8 reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 67
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001206927.2(DNAH8):c.10141-4del rs11291395 0.51174
NM_001206927.2(DNAH8):c.13119A>G (p.Leu4373=) rs3737094 0.40497
NM_001206927.2(DNAH8):c.13054-17T>C rs3737095 0.40469
NM_001206927.2(DNAH8):c.13462A>G (p.Ile4488Val) rs10484847 0.14280
NM_001206927.2(DNAH8):c.3034+9T>C rs12192604 0.13807
NM_001206927.2(DNAH8):c.11511G>A (p.Arg3837=) rs61748646 0.02251
NM_001206927.2(DNAH8):c.11331T>A (p.Thr3777=) rs75954496 0.00945
NM_001206927.2(DNAH8):c.8338A>G (p.Ile2780Val) rs116401640 0.00421
NM_001206927.2(DNAH8):c.12567A>C (p.Glu4189Asp) rs61757618 0.00314
NM_001206927.2(DNAH8):c.11340A>G (p.Leu3780=) rs113024778 0.00312
NM_001206927.2(DNAH8):c.2526G>A (p.Gln842=) rs141289823 0.00282
NM_001206927.2(DNAH8):c.14100G>T (p.Val4700=) rs113990988 0.00263
NM_001206927.2(DNAH8):c.9574A>G (p.Met3192Val) rs140935840 0.00213
NM_001206927.2(DNAH8):c.13214+10T>C rs112998568 0.00210
NM_001206927.2(DNAH8):c.13381C>T (p.Arg4461Cys) rs143714496 0.00205
NM_001206927.2(DNAH8):c.5527G>C (p.Asp1843His) rs61758415 0.00195
NM_001206927.2(DNAH8):c.8909C>T (p.Ser2970Phe) rs150571615 0.00161
NM_001206927.2(DNAH8):c.13214C>T (p.Thr4405Met) rs115630842 0.00146
NM_001206927.2(DNAH8):c.6856A>G (p.Ser2286Gly) rs113909197 0.00146
NM_001206927.2(DNAH8):c.10818G>A (p.Thr3606=) rs79890174 0.00140
NM_001206927.2(DNAH8):c.10290A>G (p.Ser3430=) rs140024206 0.00136
NM_001206927.2(DNAH8):c.8088A>G (p.Leu2696=) rs59600851 0.00104
NM_001206927.2(DNAH8):c.13747C>T (p.Arg4583Cys) rs144505769 0.00087
NM_001206927.2(DNAH8):c.2096G>A (p.Arg699His) rs141983502 0.00067
NM_001206927.2(DNAH8):c.7774C>T (p.Arg2592Trp) rs113332942 0.00064
NM_001206927.2(DNAH8):c.9673C>A (p.Gln3225Lys) rs138703233 0.00063
NM_001206927.2(DNAH8):c.7335T>C (p.Ala2445=) rs144391737 0.00050
NM_001206927.2(DNAH8):c.8583+10G>T rs146573461 0.00043
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.8238G>C (p.Val2746=) rs147418086 0.00039
NM_001206927.2(DNAH8):c.2804A>G (p.His935Arg) rs150379318 0.00038
NM_001206927.2(DNAH8):c.4512C>T (p.Thr1504=) rs200564814 0.00033
NM_001206927.2(DNAH8):c.737C>T (p.Ala246Val) rs146560083 0.00026
NM_001206927.2(DNAH8):c.9277A>G (p.Ile3093Val) rs139533720 0.00022
NM_001206927.2(DNAH8):c.11865G>T (p.Glu3955Asp) rs377043320 0.00020
NM_001206927.2(DNAH8):c.7969T>C (p.Phe2657Leu) rs372849137 0.00020
NM_001206927.2(DNAH8):c.12951+7G>A rs565030663 0.00014
NM_001206927.2(DNAH8):c.9194+1G>A rs144711161 0.00013
NM_001206927.2(DNAH8):c.7068G>T (p.Thr2356=) rs760793116 0.00011
NM_001206927.2(DNAH8):c.6847C>T (p.Leu2283=) rs200508313 0.00010
NM_001206927.2(DNAH8):c.2946G>A (p.Lys982=) rs146331687 0.00009
NM_001206927.2(DNAH8):c.3129T>A (p.Asp1043Glu) rs573755164 0.00009
NM_001206927.2(DNAH8):c.10685C>T (p.Thr3562Met) rs373914023 0.00006
NM_001206927.2(DNAH8):c.6369T>C (p.Pro2123=) rs759664111 0.00006
NM_001206927.2(DNAH8):c.2083C>G (p.His695Asp) rs200737379 0.00004
NM_001206927.2(DNAH8):c.1007A>C (p.Asn336Thr) rs111566149 0.00002
NM_001206927.2(DNAH8):c.10790+4G>A rs571129029 0.00001
NM_001206927.2(DNAH8):c.4540G>C (p.Glu1514Gln) rs1407889028 0.00001
NM_001206927.2(DNAH8):c.10525-15TCT[2] rs748043587
NM_001206927.2(DNAH8):c.10582G>A (p.Ala3528Thr)
NM_001206927.2(DNAH8):c.11169T>C (p.Leu3723=)
NM_001206927.2(DNAH8):c.11182C>T (p.Pro3728Ser) rs138016358
NM_001206927.2(DNAH8):c.11184C>G (p.Pro3728=) rs114401631
NM_001206927.2(DNAH8):c.11184C>T (p.Pro3728=)
NM_001206927.2(DNAH8):c.11714del (p.Gly3905fs)
NM_001206927.2(DNAH8):c.12248+9A>G
NM_001206927.2(DNAH8):c.12835-4T>C
NM_001206927.2(DNAH8):c.1294-6del
NM_001206927.2(DNAH8):c.13748G>T (p.Arg4583Leu) rs139227429
NM_001206927.2(DNAH8):c.2260-4dup
NM_001206927.2(DNAH8):c.2267dup (p.Asp757fs)
NM_001206927.2(DNAH8):c.673A>G (p.Asn225Asp)
NM_001206927.2(DNAH8):c.6888A>G (p.Gln2296=)
NM_001206927.2(DNAH8):c.8313G>A (p.Leu2771=)
NM_001206927.2(DNAH8):c.8832G>A (p.Ser2944=)
NM_001206927.2(DNAH8):c.9459A>G (p.Glu3153=)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.