ClinVar Miner

List of variants in gene IQSEC2 reported as benign by GeneDx

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Gene type:
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Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_001111125.3(IQSEC2):c.2298-258A>G rs4830361 0.96679
NM_001111125.3(IQSEC2):c.737+12499A>G rs6529669 0.23864
NM_001111125.3(IQSEC2):c.3115+218T>G rs111902282 0.11266
NM_001111125.3(IQSEC2):c.4104G>A (p.Leu1368=) rs184087864 0.07175
NM_001111125.3(IQSEC2):c.3555A>C (p.Pro1185=) rs1315062158 0.05436
NM_001111125.3(IQSEC2):c.999+51C>T rs75167079 0.03998
NM_001111125.3(IQSEC2):c.737+170G>A rs143266331 0.03205
NM_001111125.3(IQSEC2):c.2297+14G>A rs17002631 0.02684
NM_001111125.3(IQSEC2):c.477G>A (p.Leu159=) rs185512321 0.02235
NM_001111125.3(IQSEC2):c.1641G>A (p.Ala547=) rs61745228 0.02162
NM_001111125.3(IQSEC2):c.4408G>A (p.Ala1470Thr) rs191886831 0.00894
NM_001111125.3(IQSEC2):c.3015+14G>C rs189183148 0.00462
NM_001111125.3(IQSEC2):c.3277+18G>A rs143966238 0.00306
NM_001111125.3(IQSEC2):c.435C>T (p.Thr145=) rs782726368 0.00101
NM_001111125.3(IQSEC2):c.3990G>A (p.Gly1330=) rs371450118 0.00097
NM_001111125.3(IQSEC2):c.2508G>A (p.Ala836=) rs2274308 0.00060
NM_001111125.3(IQSEC2):c.2571C>A (p.Ile857=) rs146979083 0.00046
NM_001111125.3(IQSEC2):c.222G>C (p.Arg74=) rs781805662 0.00028
NM_001111125.3(IQSEC2):c.2322T>C (p.Tyr774=) rs147706810 0.00017
NM_001111125.3(IQSEC2):c.999+4C>T rs199648681 0.00012
NM_001111125.3(IQSEC2):c.1648C>G (p.Pro550Ala) rs782469479 0.00010
NM_001111125.3(IQSEC2):c.2937C>T (p.Tyr979=) rs191305900 0.00004
NM_001111125.3(IQSEC2):c.1498G>C (p.Glu500Gln) rs202076203 0.00002
NM_001111125.3(IQSEC2):c.4022G>A (p.Arg1341Lys) rs957057964 0.00002
NM_001111125.3(IQSEC2):c.669C>T (p.Thr223=) rs782083256 0.00001
NM_001111125.3(IQSEC2):c.1000-259del rs61173462
NM_001111125.3(IQSEC2):c.1401+186_1401+187insTTTTCC rs370967301
NM_001111125.3(IQSEC2):c.1401+199del rs57468463
NM_001111125.3(IQSEC2):c.1402-11C>A rs187186062
NM_001111125.3(IQSEC2):c.1402-65C>T rs7886988
NM_001111125.3(IQSEC2):c.2297+228C>G rs5933562
NM_001111125.3(IQSEC2):c.2890-56A>C rs2274307
NM_001111125.3(IQSEC2):c.3278-158A>G rs2296541
NM_001111125.3(IQSEC2):c.737+11962CTCC[5] rs200286632

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