ClinVar Miner

List of variants in gene FRAS1 reported as benign for autosomal recessive disease

Included ClinVar conditions (1196):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 125
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_025074.7(FRAS1):c.10649-29T>A rs931604 0.99498
NM_025074.7(FRAS1):c.470-35T>C rs1017646 0.97862
NM_025074.7(FRAS1):c.7132A>G (p.Lys2378Glu) rs7684722 0.97162
NM_025074.7(FRAS1):c.7371+11T>C rs7664505 0.95846
NM_025074.7(FRAS1):c.604-8G>A rs2867014 0.93589
NM_025074.7(FRAS1):c.1947T>C (p.His649=) rs345514 0.79008
NM_025074.7(FRAS1):c.6468C>T (p.His2156=) rs753752 0.67410
NM_025074.7(FRAS1):c.*2489T>C rs11098227 0.64399
NM_025074.7(FRAS1):c.*2154C>T rs3811747 0.63908
NM_025074.7(FRAS1):c.*2700G>A rs11098228 0.61498
NM_025074.7(FRAS1):c.10696G>A (p.Val3566Ile) rs931606 0.51866
NM_025074.7(FRAS1):c.9116-11T>C rs7677541 0.51261
NM_025074.7(FRAS1):c.9116-5C>G rs7695038 0.50468
NM_025074.7(FRAS1):c.95A>G (p.Asp32Gly) rs4859905 0.50277
NM_025074.7(FRAS1):c.2450C>T (p.Ala817Val) rs6835769 0.43382
NM_025074.7(FRAS1):c.3151+14_3151+15dup rs398092530 0.38519
NM_025074.7(FRAS1):c.7110C>T (p.His2370=) rs7660664 0.38360
NM_025074.7(FRAS1):c.8439C>T (p.Asp2813=) rs11098194 0.32564
NM_025074.7(FRAS1):c.7011G>A (p.Ala2337=) rs6851427 0.32517
NM_025074.7(FRAS1):c.1396T>A (p.Leu466Ile) rs12504081 0.31848
NM_025074.7(FRAS1):c.9808A>C (p.Arg3270=) rs3749488 0.31772
NM_025074.7(FRAS1):c.5366+13T>G rs2170899 0.31001
NM_025074.7(FRAS1):c.604-132G>A rs6856362 0.30120
NM_025074.7(FRAS1):c.*282A>T rs3749485 0.24962
NM_025074.7(FRAS1):c.108+2546T>C rs10008489 0.24570
NM_025074.7(FRAS1):c.3406G>A (p.Glu1136Lys) rs12512164 0.24213
NM_025074.7(FRAS1):c.8745C>T (p.Phe2915=) rs41327848 0.23030
NM_025074.7(FRAS1):c.7254A>G (p.Lys2418=) rs34840208 0.22689
NM_025074.7(FRAS1):c.6444C>T (p.Thr2148=) rs17003235 0.21846
NM_025074.7(FRAS1):c.*33T>A rs72659058 0.18560
NM_025074.7(FRAS1):c.9116-6C>T rs76630865 0.18150
NM_025074.7(FRAS1):c.10377C>T (p.Thr3459=) rs3749487 0.18004
NM_025074.7(FRAS1):c.4635G>A (p.Pro1545=) rs78575519 0.17765
NM_025074.7(FRAS1):c.-23C>T rs34237418 0.15546
NM_025074.7(FRAS1):c.10153T>G (p.Tyr3385Asp) rs35933858 0.14412
NM_025074.7(FRAS1):c.9252G>T (p.Arg3084=) rs11933630 0.14408
NM_025074.7(FRAS1):c.10389+11C>T rs74632598 0.14352
NM_025074.7(FRAS1):c.10683A>T (p.Glu3561Asp) rs931605 0.14336
NM_025074.7(FRAS1):c.*1814G>A rs17003321 0.13590
NM_025074.7(FRAS1):c.10877T>C (p.Val3626Ala) rs34670941 0.12788
NM_025074.7(FRAS1):c.*1301G>A rs3210826 0.12730
NM_025074.7(FRAS1):c.1617A>G (p.Arg539=) rs345528 0.11760
NM_025074.7(FRAS1):c.-65T>C rs6832285 0.08887
NM_025074.7(FRAS1):c.*1995G>T rs72873318 0.08697
NM_025074.7(FRAS1):c.3312T>C (p.Ser1104=) rs35774552 0.06352
NM_025074.7(FRAS1):c.6924C>T (p.Val2308=) rs13123710 0.05675
NM_025074.7(FRAS1):c.2128A>C (p.Ile710Leu) rs345512 0.04568
NM_025074.7(FRAS1):c.2575+15G>A rs79624813 0.04419
NM_025074.7(FRAS1):c.160G>C (p.Asp54His) rs17003071 0.03918
NM_025074.7(FRAS1):c.*3092A>G rs17003335 0.03563
NM_025074.7(FRAS1):c.*388C>G rs75970105 0.03561
NM_025074.7(FRAS1):c.6608C>T (p.Thr2203Ile) rs114373602 0.02814
NM_025074.7(FRAS1):c.6691G>A (p.Gly2231Arg) rs76623027 0.02812
NM_025074.7(FRAS1):c.6754G>A (p.Ala2252Thr) rs78404051 0.02812
NM_025074.7(FRAS1):c.6010+13C>T rs75774018 0.02805
NM_025074.7(FRAS1):c.6039T>C (p.Ser2013=) rs76472539 0.02805
NM_025074.7(FRAS1):c.6010+10G>A rs78537685 0.02804
NM_025074.7(FRAS1):c.682T>C (p.Tyr228His) rs7682296 0.02766
NM_025074.7(FRAS1):c.625C>T (p.Pro209Ser) rs7699637 0.02763
NM_025074.7(FRAS1):c.470-4C>G rs59429199 0.02676
NM_025074.7(FRAS1):c.7758C>T (p.Ile2586=) rs77602894 0.02660
NM_025074.7(FRAS1):c.7701G>A (p.Lys2567=) rs79849142 0.02656
NM_025074.7(FRAS1):c.*751T>G rs6832584 0.02441
NM_025074.7(FRAS1):c.6010+8A>G rs7670555 0.02371
NM_025074.7(FRAS1):c.6252C>T (p.Asn2084=) rs114956797 0.02261
NM_025074.7(FRAS1):c.*78G>T rs77632937 0.02198
NM_025074.7(FRAS1):c.7633G>A (p.Asp2545Asn) rs4388111 0.02134
NM_025074.7(FRAS1):c.3068G>A (p.Gly1023Glu) rs17459809 0.01892
NM_025074.7(FRAS1):c.3124G>A (p.Ala1042Thr) rs114077522 0.01873
NM_025074.7(FRAS1):c.981+9C>T rs112081709 0.01835
NM_025074.7(FRAS1):c.*1289G>A rs113324102 0.01731
NM_025074.7(FRAS1):c.2660C>G (p.Thr887Ser) rs74510691 0.01688
NM_025074.7(FRAS1):c.727A>G (p.Ile243Val) rs6848030 0.01516
NM_025074.7(FRAS1):c.1286C>A (p.Ser429Tyr) rs6838959 0.01491
NM_025074.7(FRAS1):c.308A>T (p.Glu103Val) rs78711748 0.01459
NM_025074.7(FRAS1):c.979C>T (p.Arg327Trp) rs61999335 0.01454
NM_025074.7(FRAS1):c.11717T>C (p.Ile3906Thr) rs61748814 0.01397
NM_025074.7(FRAS1):c.5208T>C (p.Leu1736=) rs35608396 0.01318
NM_025074.7(FRAS1):c.8417C>T (p.Thr2806Met) rs114190041 0.01251
NM_025074.7(FRAS1):c.10230C>T (p.Tyr3410=) rs34034599 0.01250
NM_025074.7(FRAS1):c.9955C>G (p.Gln3319Glu) rs78619145 0.01249
NM_025074.7(FRAS1):c.9759A>G (p.Pro3253=) rs61741742 0.01240
NM_025074.7(FRAS1):c.10494C>T (p.Thr3498=) rs149604281 0.01195
NM_025074.7(FRAS1):c.1769T>C (p.Met590Thr) rs35030041 0.01189
NM_025074.7(FRAS1):c.1416C>T (p.Cys472=) rs35690113 0.01114
NM_025074.7(FRAS1):c.3951G>A (p.Leu1317=) rs76107832 0.01090
NM_025074.7(FRAS1):c.*2811T>A rs114574352 0.01027
NM_025074.7(FRAS1):c.7074C>T (p.Gly2358=) rs7660641 0.01013
NM_025074.7(FRAS1):c.6124C>T (p.Pro2042Ser) rs60539739 0.01012
NM_025074.7(FRAS1):c.10278C>T (p.Ile3426=) rs34678339 0.00987
NM_025074.7(FRAS1):c.8959-11A>G rs112232078 0.00985
NM_025074.7(FRAS1):c.518G>A (p.Arg173Gln) rs147332320 0.00963
NM_025074.7(FRAS1):c.11720G>T (p.Gly3907Val) rs61748815 0.00933
NM_025074.7(FRAS1):c.10269G>T (p.Pro3423=) rs34806279 0.00927
NM_025074.7(FRAS1):c.10002G>A (p.Glu3334=) rs80346282 0.00915
NM_025074.7(FRAS1):c.4940C>T (p.Thr1647Ile) rs34271211 0.00909
NM_025074.7(FRAS1):c.*708C>A rs111636328 0.00860
NM_025074.7(FRAS1):c.1710C>T (p.Pro570=) rs17003124 0.00783
NM_025074.7(FRAS1):c.*709G>A rs115458096 0.00723
NM_025074.7(FRAS1):c.*2370G>A rs116617672 0.00710
NM_025074.7(FRAS1):c.4143T>C (p.Leu1381=) rs113301188 0.00658
NM_025074.7(FRAS1):c.10598G>A (p.Arg3533Gln) rs115878217 0.00648
NM_025074.7(FRAS1):c.688-13T>C rs144657066 0.00629
NM_025074.7(FRAS1):c.9183G>A (p.Ala3061=) rs139589570 0.00463
NM_025074.7(FRAS1):c.9853C>T (p.His3285Tyr) rs182196851 0.00436
NM_025074.7(FRAS1):c.8215G>A (p.Ala2739Thr) rs192476468 0.00426
NM_025074.7(FRAS1):c.10160T>C (p.Leu3387Pro) rs137982616 0.00365
NM_025074.7(FRAS1):c.*258G>A rs114161007 0.00361
NM_025074.7(FRAS1):c.8832C>T (p.Ser2944=) rs114854941 0.00296
NM_025074.7(FRAS1):c.4969+9A>C rs147019759 0.00213
NM_025074.7(FRAS1):c.7652A>G (p.Gln2551Arg) rs183712679 0.00169
NM_025074.7(FRAS1):c.789+12T>G rs142206350 0.00142
NM_025074.7(FRAS1):c.*503T>C rs3749484 0.00098
NM_025074.7(FRAS1):c.3010+14_3010+29del rs112289727 0.00091
NM_025074.7(FRAS1):c.1072-5C>T rs570183677 0.00006
NM_025074.7(FRAS1):c.*2824_*2825insTTTT rs397724155
NM_025074.7(FRAS1):c.*518dup rs397752464
NM_025074.7(FRAS1):c.*731C>G rs116483248
NM_025074.7(FRAS1):c.*808C>T rs59820455
NM_025074.7(FRAS1):c.-257G>T rs78363185
NM_025074.7(FRAS1):c.10648+25del rs397994139
NM_025074.7(FRAS1):c.11445+68_11445+69del rs3062747
NM_025074.7(FRAS1):c.2060A>G (p.Asp687Gly) rs345513
NM_025074.7(FRAS1):c.2313G>T (p.Pro771=) rs396790
NM_025074.7(FRAS1):c.380C>G (p.Pro127Arg) rs147709711

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.