ClinVar Miner

List of variants in gene DNAH8 reported as likely benign for not provided

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Gene type:
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Total variants: 45
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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.12264C>T (p.Asp4088=) rs61748647 0.00611
NM_001206927.2(DNAH8):c.4084-4G>T rs61748602 0.00549
NM_001206927.2(DNAH8):c.8339T>C (p.Ile2780Thr) rs142328376 0.00463
NM_001206927.2(DNAH8):c.4401G>A (p.Thr1467=) rs45622336 0.00347
NM_001206927.2(DNAH8):c.4383G>A (p.Leu1461=) rs145272110 0.00317
NM_001206927.2(DNAH8):c.14100G>T (p.Val4700=) rs113990988 0.00263
NM_001206927.2(DNAH8):c.8724G>A (p.Glu2908=) rs149787191 0.00261
NM_001206927.2(DNAH8):c.9987C>T (p.Ser3329=) rs150857304 0.00235
NM_001206927.2(DNAH8):c.2174C>G (p.Ala725Gly) rs61757621 0.00170
NM_001206927.2(DNAH8):c.10591C>T (p.Leu3531=) rs150730516 0.00152
NM_001206927.2(DNAH8):c.11379G>A (p.Thr3793=) rs112903128 0.00137
NM_001206927.2(DNAH8):c.13992G>C (p.Leu4664=) rs371719991 0.00046
NM_001206927.2(DNAH8):c.8238G>C (p.Val2746=) rs147418086 0.00039
NM_001206927.2(DNAH8):c.4512C>T (p.Thr1504=) rs200564814 0.00033
NM_001206927.2(DNAH8):c.5545A>T (p.Ile1849Leu) rs145036630 0.00025
NM_001206927.2(DNAH8):c.6273T>C (p.Asp2091=) rs146195264 0.00014
NM_001206927.2(DNAH8):c.8880A>T (p.Pro2960=) rs774972147 0.00007
NM_001206927.2(DNAH8):c.13083G>A (p.Pro4361=) rs143472136 0.00006
NM_001206927.2(DNAH8):c.7584C>T (p.Pro2528=) rs748939836 0.00005
NM_001206927.2(DNAH8):c.7482A>G (p.Ala2494=) rs375517878 0.00004
NM_001206927.2(DNAH8):c.12526-3C>T rs374461538 0.00003
NM_001206927.2(DNAH8):c.552G>A (p.Ala184=) rs201672902 0.00002
NM_001206927.2(DNAH8):c.5547A>C (p.Ile1849=) rs776384266 0.00001
NM_001206927.2(DNAH8):c.6705C>T (p.Asp2235=) rs1199187878 0.00001
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.10674T>C (p.Asn3558=) rs1160474440
NM_001206927.2(DNAH8):c.11184C>G (p.Pro3728=) rs114401631
NM_001206927.2(DNAH8):c.1134G>A (p.Glu378=)
NM_001206927.2(DNAH8):c.12387C>T (p.Cys4129=) rs1761899691
NM_001206927.2(DNAH8):c.12562C>T (p.Leu4188=) rs1583484448
NM_001206927.2(DNAH8):c.12822C>T (p.His4274=) rs1480630966
NM_001206927.2(DNAH8):c.2673T>C (p.Ser891=) rs1583012566
NM_001206927.2(DNAH8):c.3822T>C (p.Val1274=) rs1338876432
NM_001206927.2(DNAH8):c.5160C>G (p.Ala1720=) rs200767977
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.5646A>G (p.Ser1882=) rs1583186990
NM_001206927.2(DNAH8):c.5727A>G (p.Pro1909=) rs1583187318
NM_001206927.2(DNAH8):c.6675A>G (p.Glu2225=) rs1583220331
NM_001206927.2(DNAH8):c.816G>A (p.Arg272=) rs1582865584
NM_001206927.2(DNAH8):c.953-8C>T rs1400806860
NM_001206927.2(DNAH8):c.9762G>A (p.Val3254=) rs776814257

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