ClinVar Miner

List of variants studied for Slowed nerve conduction velocity, autosomal dominant

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Total variants: 29
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HGVS dbSNP
NM_014629.4(ARHGEF10):c.1075+13A>G rs4543586
NM_014629.4(ARHGEF10):c.1110G>C (p.Leu370Phe) rs9657362
NM_014629.4(ARHGEF10):c.1113C>T (p.Phe371=) rs34655804
NM_014629.4(ARHGEF10):c.121G>T (p.Glu41Ter)
NM_014629.4(ARHGEF10):c.1260+4C>T rs79548709
NM_014629.4(ARHGEF10):c.133C>T (p.Gln45Ter) rs1467438651
NM_014629.4(ARHGEF10):c.1343A>G (p.Glu448Gly)
NM_014629.4(ARHGEF10):c.141A>C (p.Pro47=) rs4875950
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.1991T>C (p.Met664Thr) rs34319003
NM_014629.4(ARHGEF10):c.2063G>A (p.Ser688Asn) rs143290224
NM_014629.4(ARHGEF10):c.2098G>A (p.Val700Ile) rs2294039
NM_014629.4(ARHGEF10):c.2134G>T (p.Ala712Ser) rs1057523214
NM_014629.4(ARHGEF10):c.2143+13T>G rs2294041
NM_014629.4(ARHGEF10):c.2259+8T>C rs1015159398
NM_014629.4(ARHGEF10):c.2460C>G (p.Asn820Lys)
NM_014629.4(ARHGEF10):c.2812G>A (p.Val938Ile) rs61752020
NM_014629.4(ARHGEF10):c.2909C>T (p.Thr970Met) rs35925274
NM_014629.4(ARHGEF10):c.3398-16A>G rs7832438
NM_014629.4(ARHGEF10):c.38-10T>C rs138713415
NM_014629.4(ARHGEF10):c.3869C>T (p.Ser1290Leu)
NM_014629.4(ARHGEF10):c.387A>G (p.Val129=) rs749822
NM_014629.4(ARHGEF10):c.3964_3965dup (p.Arg1323fs) rs1563343679
NM_014629.4(ARHGEF10):c.401C>T (p.Ala134Val) rs151080025
NM_014629.4(ARHGEF10):c.474C>T (p.Asp158=) rs147914724
NM_014629.4(ARHGEF10):c.541A>G (p.Thr181Ala)
NM_014629.4(ARHGEF10):c.630G>A (p.Glu210=) rs7003969
NM_014629.4(ARHGEF10):c.995C>T (p.Thr332Ile) rs28940281

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