ClinVar Miner

List of variants in gene ARHGEF10 studied for Autosomal dominant slowed nerve conduction velocity

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Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_014629.4(ARHGEF10):c.3398-16A>G rs7832438 0.93211
NM_014629.4(ARHGEF10):c.1075+13A>G rs4543586 0.65298
NM_014629.4(ARHGEF10):c.2143+13T>G rs2294041 0.28589
NM_014629.4(ARHGEF10):c.630G>A (p.Glu210=) rs7003969 0.20504
NM_014629.4(ARHGEF10):c.1110G>C (p.Leu370Phe) rs9657362 0.11648
NM_014629.4(ARHGEF10):c.387A>G (p.Val129=) rs749822 0.05521
NM_014629.4(ARHGEF10):c.1113C>T (p.Phe371=) rs34655804 0.04733
NM_014629.4(ARHGEF10):c.2098G>A (p.Val700Ile) rs2294039 0.03098
NM_014629.4(ARHGEF10):c.1991T>C (p.Met664Thr) rs34319003 0.00800
NM_014629.4(ARHGEF10):c.2812G>A (p.Val938Ile) rs61752020 0.00620
NM_014629.4(ARHGEF10):c.1260+4C>T rs79548709 0.00566
NM_014629.4(ARHGEF10):c.38-10T>C rs138713415 0.00351
NM_014629.4(ARHGEF10):c.401C>T (p.Ala134Val) rs151080025 0.00082
NM_014629.4(ARHGEF10):c.474C>T (p.Asp158=) rs147914724 0.00082
NM_014629.4(ARHGEF10):c.2063G>A (p.Ser688Asn) rs143290224 0.00051
NM_014629.4(ARHGEF10):c.3098A>G (p.Glu1033Gly) rs189989926 0.00044
NM_014629.4(ARHGEF10):c.3869C>T (p.Ser1290Leu) rs150226594 0.00041
NM_014629.4(ARHGEF10):c.2909C>T (p.Thr970Met) rs35925274 0.00036
NM_014629.4(ARHGEF10):c.2460C>G (p.Asn820Lys) rs61758704 0.00009
NM_014629.4(ARHGEF10):c.1013G>C (p.Arg338Thr) rs587777712 0.00002
NM_014629.4(ARHGEF10):c.1030A>G (p.Lys344Glu)
NM_014629.4(ARHGEF10):c.1076-3_1076-2delinsTG
NM_014629.4(ARHGEF10):c.121G>T (p.Glu41Ter) rs764859351
NM_014629.4(ARHGEF10):c.133C>T (p.Gln45Ter) rs1467438651
NM_014629.4(ARHGEF10):c.1343A>G (p.Glu448Gly) rs1809808538
NM_014629.4(ARHGEF10):c.141A>C (p.Pro47=) rs4875950
NM_014629.4(ARHGEF10):c.1606del (p.Met535_Met536insTer)
NM_014629.4(ARHGEF10):c.1720G>A (p.Glu574Lys) rs1437730951
NM_014629.4(ARHGEF10):c.1812C>A (p.Tyr604Ter) rs1332591469
NM_014629.4(ARHGEF10):c.1936G>A (p.Asp646Asn)
NM_014629.4(ARHGEF10):c.2005T>G (p.Tyr669Asp)
NM_014629.4(ARHGEF10):c.2134G>T (p.Ala712Ser) rs1057523214
NM_014629.4(ARHGEF10):c.2711C>G (p.Thr904Ser)
NM_014629.4(ARHGEF10):c.343G>T (p.Glu115Ter) rs1585296361
NM_014629.4(ARHGEF10):c.3964_3965dup (p.Arg1323fs) rs1563343679
NM_014629.4(ARHGEF10):c.541A>G (p.Thr181Ala) rs746857277
NM_014629.4(ARHGEF10):c.679+2T>A
NM_014629.4(ARHGEF10):c.843+47C>G
NM_014629.4(ARHGEF10):c.990C>A (p.Asp330Glu) rs372309933
NM_014629.4(ARHGEF10):c.995C>T (p.Thr332Ile) rs28940281

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