ClinVar Miner

List of variants in gene ARHGEF10 reported by Mayo Clinic Laboratories, Mayo Clinic

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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_014629.4(ARHGEF10):c.1631A>T (p.Gln544Leu) rs148715187 0.00153
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.3589C>T (p.His1197Tyr) rs200779877 0.00026
NM_014629.4(ARHGEF10):c.3475G>A (p.Val1159Met) rs370742932 0.00013
NM_014629.4(ARHGEF10):c.2894C>T (p.Thr965Met) rs375235314 0.00008
NM_014629.4(ARHGEF10):c.3571G>A (p.Val1191Ile) rs577376669 0.00007
NM_014629.4(ARHGEF10):c.971T>C (p.Leu324Pro) rs985210714 0.00004
NM_014629.4(ARHGEF10):c.2684A>G (p.His895Arg) rs777004497 0.00003
NM_014629.4(ARHGEF10):c.3056T>A (p.Val1019Asp) rs750481483 0.00002
NM_014629.4(ARHGEF10):c.4000G>A (p.Val1334Ile) rs748072321 0.00002
NM_014629.4(ARHGEF10):c.1235T>C (p.Val412Ala) rs774258882 0.00001
NM_014629.4(ARHGEF10):c.125C>T (p.Ala42Val) rs775076236 0.00001
NM_014629.4(ARHGEF10):c.2045C>T (p.Ala682Val) rs1057518334 0.00001
NM_014629.4(ARHGEF10):c.2838G>T (p.Glu946Asp) rs768339597 0.00001
NM_014629.4(ARHGEF10):c.2993C>G (p.Ser998Cys) rs1812929298 0.00001
NM_014629.4(ARHGEF10):c.3349C>A (p.His1117Asn) rs1006898043 0.00001
NM_014629.4(ARHGEF10):c.167G>A (p.Gly56Glu) rs1374095120
NM_014629.4(ARHGEF10):c.3020C>T (p.Ser1007Phe) rs1812932469
NM_014629.4(ARHGEF10):c.3161C>T (p.Thr1054Met) rs141078341
NM_014629.4(ARHGEF10):c.577C>T (p.Leu193Phe) rs373032561
NM_014629.4(ARHGEF10):c.898T>G (p.Leu300Val) rs754510892

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