ClinVar Miner

List of variants in gene ALG8 reported as benign for not provided

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_024079.5(ALG8):c.478+35A>T rs518624 0.99999
NM_024079.5(ALG8):c.1039-284A>C rs11825396 0.99868
NM_024079.4(ALG8):c.*20A>G rs1263505 0.86211
NM_024079.5(ALG8):c.96-263G>A rs579088 0.85973
NC_000011.10:g.78100680T>C rs2845556 0.67338
NM_024079.5(ALG8):c.547-204T>C rs653721 0.66755
NM_024079.5(ALG8):c.898+139C>T rs624350 0.62975
NM_024079.5(ALG8):c.175-239G>C rs7951150 0.44753
NM_024079.5(ALG8):c.673+37T>C rs10899440 0.37163
NM_024079.5(ALG8):c.546+180C>T rs12146488 0.37149
NM_024079.5(ALG8):c.1038+320A>G rs10751281 0.37135
NM_024079.5(ALG8):c.1179-277C>T rs611331 0.22119
NM_024079.5(ALG8):c.174+155G>T rs553576 0.21996
NM_024079.5(ALG8):c.546+270A>G rs1783517 0.21983
NM_024079.5(ALG8):c.547-259G>A rs653368 0.21974
NM_024079.5(ALG8):c.778-228G>T rs563013 0.21957
NM_024079.5(ALG8):c.674-29T>C rs572693 0.21953
NM_024079.5(ALG8):c.547-70T>C rs678277 0.21947
NM_024079.5(ALG8):c.899-43A>G rs1783515 0.21923
NM_024079.5(ALG8):c.369-249A>C rs7105633 0.21917
NM_024079.5(ALG8):c.479-294A>G rs61900233 0.21917
NM_024079.5(ALG8):c.174+259dup rs111964866 0.21914
NM_024079.5(ALG8):c.899-46A>G rs1789032 0.21912
NM_024079.5(ALG8):c.96-198G>A rs578903 0.21900
NM_024079.5(ALG8):c.174+268G>A rs1815861 0.21889
NM_024079.5(ALG8):c.665A>G (p.Asn222Ser) rs665278 0.17617
NM_024079.5(ALG8):c.1277-98G>A rs660061 0.17517
NM_024079.5(ALG8):c.674-31C>T rs61566223 0.07574
NM_024079.5(ALG8):c.1178+234T>C rs112629321 0.07562
NM_024079.5(ALG8):c.1178+122_1178+125dup rs3831385 0.06679
NC_000011.10:g.78100847T>C rs11237385 0.05463
NM_024079.5(ALG8):c.862T>C (p.Leu288=) rs61995924 0.04685
NM_024079.5(ALG8):c.174+238T>C rs188432893 0.02278
NM_024079.5(ALG8):c.1316T>C (p.Ile439Thr) rs17825668 0.02180
NC_000011.10:g.78100817C>T rs17136231 0.02132
NM_024079.5(ALG8):c.1350-82A>T rs113781975 0.02119
NM_024079.5(ALG8):c.1039-5T>C rs112211908 0.02114
NM_024079.5(ALG8):c.1179-241A>G rs111248015 0.02022
NM_024079.5(ALG8):c.898+36T>C rs112355034 0.01871
NM_024079.5(ALG8):c.803G>A (p.Arg268Gln) rs61995925 0.01476
NM_024079.5(ALG8):c.896T>C (p.Ile299Thr) rs61995922 0.00615
NM_024079.5(ALG8):c.588A>C (p.Leu196=) rs562915665 0.00003
NC_000011.10:g.78100755dup rs3841745
NC_000011.10:g.78139757G>T rs615116
NC_000011.10:g.78139763C>T rs582266
NC_000011.10:g.78139778C>T rs2156785
NM_024079.5(ALG8):c.1039-276AT[10] rs57228944
NM_024079.5(ALG8):c.1039-276AT[11] rs57228944
NM_024079.5(ALG8):c.1039-276AT[13] rs57228944
NM_024079.5(ALG8):c.1039-276AT[14] rs57228944
NM_024079.5(ALG8):c.1039-276AT[9] rs57228944
NM_024079.5(ALG8):c.174+30del rs59662312
NM_024079.5(ALG8):c.368+73C>T rs498278
NM_024079.5(ALG8):c.369-339dup rs11431514
NM_024079.5(ALG8):c.479-179_479-169del rs1484151842
NM_024079.5(ALG8):c.479-179_479-171del rs374346497
NM_024079.5(ALG8):c.479-304G>A rs139548337
NM_024079.5(ALG8):c.777+164G>T rs4991879
NM_024079.5(ALG8):c.777+164_777+167del rs200682684
NM_024079.5(ALG8):c.777+164_777+168del rs371530185
NM_024079.5(ALG8):c.777+187A>G rs570219
NM_024079.5(ALG8):c.777+8_777+10dup rs111652232
NM_024079.5(ALG8):c.777+8_777+11dup rs111652232
NM_024079.5(ALG8):c.777+8dup rs111652232
NM_024079.5(ALG8):c.96-291_96-287dup rs1192507872
NM_024079.5(ALG8):c.96-291_96-288dup rs1192507872

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