ClinVar Miner

List of variants in gene FRAS1 reported as benign for auditory system disease

Included ClinVar conditions (549):
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Gene type:
ClinVar version:
Total variants: 122
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HGVS dbSNP
NM_025074.7(FRAS1):c.*1289G>A rs113324102
NM_025074.7(FRAS1):c.*1301G>A rs3210826
NM_025074.7(FRAS1):c.*1814G>A rs17003321
NM_025074.7(FRAS1):c.*1995G>T rs72873318
NM_025074.7(FRAS1):c.*2154C>T rs3811747
NM_025074.7(FRAS1):c.*2370G>A rs116617672
NM_025074.7(FRAS1):c.*2489T>C rs11098227
NM_025074.7(FRAS1):c.*258G>A
NM_025074.7(FRAS1):c.*2700G>A rs11098228
NM_025074.7(FRAS1):c.*2811T>A rs114574352
NM_025074.7(FRAS1):c.*2824_*2825insTTTT rs397724155
NM_025074.7(FRAS1):c.*282A>T rs3749485
NM_025074.7(FRAS1):c.*3092A>G rs17003335
NM_025074.7(FRAS1):c.*33T>A rs72659058
NM_025074.7(FRAS1):c.*388C>G rs75970105
NM_025074.7(FRAS1):c.*503T>C rs3749484
NM_025074.7(FRAS1):c.*518dup rs397752464
NM_025074.7(FRAS1):c.*708C>A rs111636328
NM_025074.7(FRAS1):c.*709G>A rs115458096
NM_025074.7(FRAS1):c.*731C>G rs116483248
NM_025074.7(FRAS1):c.*751T>G rs6832584
NM_025074.7(FRAS1):c.*78G>T rs77632937
NM_025074.7(FRAS1):c.*808C>T rs59820455
NM_025074.7(FRAS1):c.-23C>T rs34237418
NM_025074.7(FRAS1):c.-257G>T rs78363185
NM_025074.7(FRAS1):c.-65T>C rs6832285
NM_025074.7(FRAS1):c.10002G>A (p.Glu3334=) rs80346282
NM_025074.7(FRAS1):c.10153T>G (p.Tyr3385Asp) rs35933858
NM_025074.7(FRAS1):c.10160T>C (p.Leu3387Pro) rs137982616
NM_025074.7(FRAS1):c.10230C>T (p.Tyr3410=) rs34034599
NM_025074.7(FRAS1):c.10269G>T (p.Pro3423=) rs34806279
NM_025074.7(FRAS1):c.10278C>T (p.Ile3426=) rs34678339
NM_025074.7(FRAS1):c.10377C>T (p.Thr3459=) rs3749487
NM_025074.7(FRAS1):c.10389+11C>T rs74632598
NM_025074.7(FRAS1):c.10494C>T (p.Thr3498=) rs149604281
NM_025074.7(FRAS1):c.10598G>A (p.Arg3533Gln) rs115878217
NM_025074.7(FRAS1):c.10648+25del rs397994139
NM_025074.7(FRAS1):c.10683A>T (p.Glu3561Asp) rs931605
NM_025074.7(FRAS1):c.10696G>A (p.Val3566Ile) rs931606
NM_025074.7(FRAS1):c.1072-5C>T
NM_025074.7(FRAS1):c.108+2546T>C rs10008489
NM_025074.7(FRAS1):c.10877T>C (p.Val3626Ala) rs34670941
NM_025074.7(FRAS1):c.11037C>G (p.Pro3679=) rs4975070
NM_025074.7(FRAS1):c.11056C>T (p.Leu3686=) rs4975139
NM_025074.7(FRAS1):c.11445+68_11445+69del rs3062747
NM_025074.7(FRAS1):c.11717T>C (p.Ile3906Thr) rs61748814
NM_025074.7(FRAS1):c.11720G>T (p.Gly3907Val) rs61748815
NM_025074.7(FRAS1):c.1286C>A (p.Ser429Tyr) rs6838959
NM_025074.7(FRAS1):c.1396T>A (p.Leu466Ile) rs12504081
NM_025074.7(FRAS1):c.1416C>T (p.Cys472=) rs35690113
NM_025074.7(FRAS1):c.160G>C (p.Asp54His) rs17003071
NM_025074.7(FRAS1):c.1617A>G (p.Arg539=) rs345528
NM_025074.7(FRAS1):c.1710C>T (p.Pro570=) rs17003124
NM_025074.7(FRAS1):c.1769T>C (p.Met590Thr) rs35030041
NM_025074.7(FRAS1):c.1947T>C (p.His649=) rs345514
NM_025074.7(FRAS1):c.2060A>G (p.Asp687Gly) rs345513
NM_025074.7(FRAS1):c.2128A>C (p.Ile710Leu) rs345512
NM_025074.7(FRAS1):c.2313G>T (p.Pro771=) rs396790
NM_025074.7(FRAS1):c.2450C>T (p.Ala817Val) rs6835769
NM_025074.7(FRAS1):c.2575+15G>A rs79624813
NM_025074.7(FRAS1):c.2660C>G (p.Thr887Ser) rs74510691
NM_025074.7(FRAS1):c.3068G>A (p.Gly1023Glu) rs17459809
NM_025074.7(FRAS1):c.308A>T (p.Glu103Val) rs78711748
NM_025074.7(FRAS1):c.3124G>A (p.Ala1042Thr) rs114077522
NM_025074.7(FRAS1):c.3151+14_3151+15dup rs398092530
NM_025074.7(FRAS1):c.3312T>C (p.Ser1104=) rs35774552
NM_025074.7(FRAS1):c.3406G>A (p.Glu1136Lys) rs12512164
NM_025074.7(FRAS1):c.380C>G (p.Pro127Arg) rs147709711
NM_025074.7(FRAS1):c.3951G>A (p.Leu1317=) rs76107832
NM_025074.7(FRAS1):c.4143T>C (p.Leu1381=) rs113301188
NM_025074.7(FRAS1):c.4635G>A (p.Pro1545=) rs78575519
NM_025074.7(FRAS1):c.470-4C>G rs59429199
NM_025074.7(FRAS1):c.4940C>T (p.Thr1647Ile) rs34271211
NM_025074.7(FRAS1):c.518G>A (p.Arg173Gln) rs147332320
NM_025074.7(FRAS1):c.5208T>C (p.Leu1736=) rs35608396
NM_025074.7(FRAS1):c.5366+13T>G rs2170899
NM_025074.7(FRAS1):c.6010+10G>A rs78537685
NM_025074.7(FRAS1):c.6010+13C>T rs75774018
NM_025074.7(FRAS1):c.6010+8A>G rs7670555
NM_025074.7(FRAS1):c.6039T>C (p.Ser2013=) rs76472539
NM_025074.7(FRAS1):c.604-132G>A rs6856362
NM_025074.7(FRAS1):c.604-8G>A rs2867014
NM_025074.7(FRAS1):c.6124C>T (p.Pro2042Ser) rs60539739
NM_025074.7(FRAS1):c.6252C>T (p.Asn2084=) rs114956797
NM_025074.7(FRAS1):c.625C>T (p.Pro209Ser) rs7699637
NM_025074.7(FRAS1):c.6444C>T (p.Thr2148=) rs17003235
NM_025074.7(FRAS1):c.6468C>T (p.His2156=) rs753752
NM_025074.7(FRAS1):c.6608C>T (p.Thr2203Ile) rs114373602
NM_025074.7(FRAS1):c.6691G>A (p.Gly2231Arg) rs76623027
NM_025074.7(FRAS1):c.6754G>A (p.Ala2252Thr) rs78404051
NM_025074.7(FRAS1):c.682T>C (p.Tyr228His) rs7682296
NM_025074.7(FRAS1):c.688-13T>C rs144657066
NM_025074.7(FRAS1):c.6924C>T (p.Val2308=) rs13123710
NM_025074.7(FRAS1):c.7011G>A (p.Ala2337=) rs6851427
NM_025074.7(FRAS1):c.7074C>T (p.Gly2358=) rs7660641
NM_025074.7(FRAS1):c.7110C>T (p.His2370=) rs7660664
NM_025074.7(FRAS1):c.7132A>G (p.Lys2378Glu) rs7684722
NM_025074.7(FRAS1):c.7254A>G (p.Lys2418=) rs34840208
NM_025074.7(FRAS1):c.727A>G (p.Ile243Val) rs6848030
NM_025074.7(FRAS1):c.7371+11T>C rs7664505
NM_025074.7(FRAS1):c.7633G>A (p.Asp2545Asn) rs4388111
NM_025074.7(FRAS1):c.7652A>G (p.Gln2551Arg) rs183712679
NM_025074.7(FRAS1):c.7701G>A (p.Lys2567=) rs79849142
NM_025074.7(FRAS1):c.7758C>T (p.Ile2586=) rs77602894
NM_025074.7(FRAS1):c.789+12T>G
NM_025074.7(FRAS1):c.8215G>A (p.Ala2739Thr) rs192476468
NM_025074.7(FRAS1):c.8417C>T (p.Thr2806Met) rs114190041
NM_025074.7(FRAS1):c.8439C>T (p.Asp2813=) rs11098194
NM_025074.7(FRAS1):c.8745C>T (p.Phe2915=) rs41327848
NM_025074.7(FRAS1):c.8959-11A>G rs112232078
NM_025074.7(FRAS1):c.9116-11T>C rs7677541
NM_025074.7(FRAS1):c.9116-5C>G rs7695038
NM_025074.7(FRAS1):c.9116-6C>T rs76630865
NM_025074.7(FRAS1):c.9183G>A (p.Ala3061=) rs139589570
NM_025074.7(FRAS1):c.9252G>T (p.Arg3084=) rs11933630
NM_025074.7(FRAS1):c.95A>G (p.Asp32Gly) rs4859905
NM_025074.7(FRAS1):c.9759A>G (p.Pro3253=) rs61741742
NM_025074.7(FRAS1):c.979C>T (p.Arg327Trp) rs61999335
NM_025074.7(FRAS1):c.9808A>C (p.Arg3270=) rs3749488
NM_025074.7(FRAS1):c.981+9C>T rs112081709
NM_025074.7(FRAS1):c.9853C>T (p.His3285Tyr) rs182196851
NM_025074.7(FRAS1):c.9955C>G (p.Gln3319Glu) rs78619145

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