ClinVar Miner

List of variants in gene ARHGEF15 reported as benign by Invitae

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Gene type:
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Total variants: 36
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HGVS dbSNP gnomAD frequency
NM_173728.4(ARHGEF15):c.2491T>C (p.Ser831Pro) rs3744647 0.64122
NM_173728.4(ARHGEF15):c.1704+12A>G rs2270445 0.58634
NM_173728.4(ARHGEF15):c.830T>C (p.Leu277Pro) rs871841 0.58202
NM_173728.4(ARHGEF15):c.177C>T (p.Thr59=) rs3744651 0.36629
NM_173728.4(ARHGEF15):c.2323C>T (p.Arg775Trp) rs79993581 0.02200
NM_173728.4(ARHGEF15):c.217C>T (p.Pro73Ser) rs9890841 0.01541
NM_173728.4(ARHGEF15):c.1827A>G (p.Glu609=) rs35204656 0.01440
NM_173728.4(ARHGEF15):c.1278G>A (p.Val426=) rs8067778 0.01338
NM_173728.4(ARHGEF15):c.1574+11C>T rs113936293 0.01284
NM_173728.4(ARHGEF15):c.570C>T (p.Thr190=) rs62637603 0.01279
NM_173728.4(ARHGEF15):c.822C>T (p.Leu274=) rs115119785 0.00507
NM_173728.4(ARHGEF15):c.2366C>A (p.Thr789Asn) rs76729434 0.00477
NM_173728.4(ARHGEF15):c.2034-19C>T rs117474192 0.00461
NM_173728.4(ARHGEF15):c.2388G>T (p.Gly796=) rs145204305 0.00310
NM_173728.4(ARHGEF15):c.67C>T (p.Arg23Cys) rs137909519 0.00294
NM_173728.4(ARHGEF15):c.1250G>T (p.Arg417Leu) rs142119277 0.00258
NM_173728.4(ARHGEF15):c.54G>A (p.Arg18=) rs138484229 0.00235
NM_173728.4(ARHGEF15):c.2494T>C (p.Ser832Pro) rs115597604 0.00205
NM_173728.4(ARHGEF15):c.2504C>A (p.Thr835Asn) rs114610832 0.00203
NM_173728.4(ARHGEF15):c.960G>A (p.Gln320=) rs112237413 0.00203
NM_173728.4(ARHGEF15):c.1638G>A (p.Arg546=) rs115756996 0.00197
NM_173728.4(ARHGEF15):c.2270-15C>T rs79687084 0.00189
NM_173728.4(ARHGEF15):c.618C>T (p.Cys206=) rs138521691 0.00154
NM_173728.4(ARHGEF15):c.1260+8C>G rs73975818 0.00113
NM_173728.4(ARHGEF15):c.2004C>T (p.Ser668=) rs142705439 0.00093
NM_173728.4(ARHGEF15):c.1260+4G>A rs199691980 0.00072
NM_173728.4(ARHGEF15):c.2337C>T (p.Ser779=) rs115332545 0.00054
NM_173728.4(ARHGEF15):c.1809G>C (p.Gly603=) rs116091376 0.00028
NM_173728.4(ARHGEF15):c.2239T>C (p.Cys747Arg) rs202083675 0.00026
NM_173728.4(ARHGEF15):c.708G>A (p.Arg236=) rs34046779 0.00021
NM_173728.4(ARHGEF15):c.930A>G (p.Gln310=) rs115530616 0.00016
NM_173728.4(ARHGEF15):c.711C>T (p.Val237=) rs537744294 0.00010
NM_173728.4(ARHGEF15):c.2298G>A (p.Ser766=) rs116448253 0.00006
NM_173728.4(ARHGEF15):c.1873-5C>T rs752190951 0.00002
NM_173728.4(ARHGEF15):c.1944G>A (p.Arg648=) rs201714597
NM_173728.4(ARHGEF15):c.2519C>A (p.Pro840Gln) rs552154823

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