ClinVar Miner

List of variants in gene ARHGEF9 reported by Ambry Genetics

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Gene type:
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Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_001353921.2(ARHGEF9):c.49A>G (p.Ile17Val) rs55868891 0.00125
NM_001353921.2(ARHGEF9):c.1113C>T (p.Gly371=) rs56375542 0.00054
NM_001353921.2(ARHGEF9):c.675G>A (p.Gln225=) rs140777637 0.00039
NM_001353921.2(ARHGEF9):c.939C>G (p.Asp313Glu) rs143490560 0.00025
NM_001353921.2(ARHGEF9):c.946-4C>A rs56398019 0.00020
NM_001353921.2(ARHGEF9):c.1330A>G (p.Ile444Val) rs141815718 0.00018
NM_001353921.2(ARHGEF9):c.1471G>A (p.Asp491Asn) rs782577519 0.00015
NM_001353921.2(ARHGEF9):c.1488G>A (p.Ser496=) rs782580975 0.00015
NM_001353921.2(ARHGEF9):c.1530A>T (p.Pro510=) rs145815177 0.00009
NM_001353921.2(ARHGEF9):c.582C>T (p.His194=) rs150129110 0.00008
NM_001353921.2(ARHGEF9):c.351G>A (p.Glu117=) rs373866956 0.00006
NM_001353921.2(ARHGEF9):c.1183A>G (p.Met395Val) rs781988728 0.00005
NM_001353921.2(ARHGEF9):c.372C>T (p.His124=) rs138198839 0.00004
NM_001353921.2(ARHGEF9):c.1011G>A (p.Gln337=) rs1330960420 0.00002
NM_001353921.2(ARHGEF9):c.105A>G (p.Ala35=) rs782666474 0.00002
NM_001353921.2(ARHGEF9):c.1452C>T (p.His484=) rs782395885 0.00002
NM_001353921.2(ARHGEF9):c.305G>A (p.Arg102Gln) rs782087438 0.00002
NM_001353921.2(ARHGEF9):c.1480G>A (p.Ala494Thr) rs1556301016 0.00001
NM_001353921.2(ARHGEF9):c.1482T>C (p.Ala494=) rs782665661 0.00001
NM_001353921.2(ARHGEF9):c.1518C>T (p.Arg506=) rs782806516 0.00001
NM_001353921.2(ARHGEF9):c.264C>T (p.Asn88=) rs782671712 0.00001
NM_001353921.2(ARHGEF9):c.366G>A (p.Glu122=) rs781834665 0.00001
NM_001353921.2(ARHGEF9):c.432G>A (p.Arg144=) rs781937951 0.00001
NM_001353921.2(ARHGEF9):c.1033C>T (p.Arg345Trp) rs869312941
NM_001353921.2(ARHGEF9):c.1084A>T (p.Ile362Phe)
NM_001353921.2(ARHGEF9):c.1115G>A (p.Arg372His) rs2048831313
NM_001353921.2(ARHGEF9):c.1142T>C (p.Val381Ala)
NM_001353921.2(ARHGEF9):c.1321G>A (p.Gly441Ser) rs2048820687
NM_001353921.2(ARHGEF9):c.1390+2T>A
NM_001353921.2(ARHGEF9):c.271C>A (p.Leu91Met)
NM_001353921.2(ARHGEF9):c.305G>T (p.Arg102Leu) rs782087438
NM_001353921.2(ARHGEF9):c.403-4A>C
NM_001353921.2(ARHGEF9):c.415C>T (p.Gln139Ter)
NM_001353921.2(ARHGEF9):c.556G>A (p.Glu186Lys) rs1602446549
NM_001353921.2(ARHGEF9):c.811C>T (p.His271Tyr) rs2050403490
NM_001353921.2(ARHGEF9):c.875del (p.Asn292fs) rs2050117690
NM_001353921.2(ARHGEF9):c.87G>A (p.Met29Ile) rs1569491685
NM_001353921.2(ARHGEF9):c.889C>T (p.Arg297Cys) rs2050115619
NM_001353921.2(ARHGEF9):c.890G>A (p.Arg297His)
NM_001353921.2(ARHGEF9):c.968G>T (p.Ser323Ile) rs1569451962
NM_001353921.2(ARHGEF9):c.995T>C (p.Met332Thr)

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