ClinVar Miner

List of variants in gene ARHGEF9 studied for not specified

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Gene type:
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Total variants: 35
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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.675G>A (p.Gln225=) rs140777637 0.00039
NM_001353921.2(ARHGEF9):c.*7C>G rs202232026 0.00027
NM_001353921.2(ARHGEF9):c.946-4C>A rs56398019 0.00020
NM_001353921.2(ARHGEF9):c.579G>A (p.Glu193=) rs56182751 0.00016
NM_001353921.2(ARHGEF9):c.885G>A (p.Lys295=) rs199625034 0.00016
NM_001353921.2(ARHGEF9):c.946-16C>T rs781867369 0.00011
NM_001353921.2(ARHGEF9):c.31-29583C>A rs370045250 0.00009
NM_001353921.2(ARHGEF9):c.582C>T (p.His194=) rs150129110 0.00008
NM_001353921.2(ARHGEF9):c.447C>T (p.Asp149=) rs782313473 0.00007
NM_001353921.2(ARHGEF9):c.351G>A (p.Glu117=) rs373866956 0.00006
NM_001353921.2(ARHGEF9):c.777G>A (p.Gln259=) rs1057522740 0.00006
NM_001353921.2(ARHGEF9):c.372C>T (p.His124=) rs138198839 0.00004
NM_001353921.2(ARHGEF9):c.564A>T (p.Gly188=) rs782187939 0.00003
NM_001353921.2(ARHGEF9):c.583-18T>G rs1057521815 0.00003
NM_001353921.2(ARHGEF9):c.31-29639A>T rs782573720 0.00002
NM_001353921.2(ARHGEF9):c.1218T>A (p.Thr406=) rs1057521807 0.00001
NM_001353921.2(ARHGEF9):c.1506C>T (p.Thr502=) rs782129771 0.00001
NM_001353921.2(ARHGEF9):c.475A>G (p.Ile159Val) rs1556389367 0.00001
NM_001353921.2(ARHGEF9):c.667C>T (p.Arg223Cys) rs782139620 0.00001
NM_001353921.2(ARHGEF9):c.668G>A (p.Arg223His) rs1556365349 0.00001
GRCh37/hg19 Xq11.1-11.2(chrX:62970571-63052696)
NM_001353921.2(ARHGEF9):c.1078-18C>T rs781901799
NM_001353921.2(ARHGEF9):c.166C>A (p.Gln56Lys) rs781823638
NM_001353921.2(ARHGEF9):c.234G>A (p.Glu78=) rs868932053
NM_001353921.2(ARHGEF9):c.266G>T (p.Gly89Val) rs797045261
NM_001353921.2(ARHGEF9):c.31-29642del rs782757577
NM_001353921.2(ARHGEF9):c.561A>T (p.Ile187=) rs1057522301
NM_001353921.2(ARHGEF9):c.726C>A (p.Ile242=) rs1556365224
NM_001353921.2(ARHGEF9):c.744T>C (p.Thr248=) rs1556365168
NM_001353921.2(ARHGEF9):c.781G>T (p.Ala261Ser) rs782497496
NM_001353921.2(ARHGEF9):c.816-12_816-11del rs781845457
NM_001353921.2(ARHGEF9):c.816-9T>C rs1057522347
NM_001353921.2(ARHGEF9):c.901A>T (p.Ile301Phe) rs1556359038
NM_001353921.2(ARHGEF9):c.948C>A (p.Gly316=) rs141158169

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