ClinVar Miner

List of variants in gene FRAS1 reported as benign for not specified

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Total variants: 66
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HGVS dbSNP gnomAD frequency
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.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.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.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.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.10877T>C (p.Val3626Ala) rs34670941 0.12788
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.160G>C (p.Asp54His) rs17003071 0.03918
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.308A>T (p.Glu103Val) rs78711748 0.01459
NM_025074.7(FRAS1):c.979C>T (p.Arg327Trp) rs61999335 0.01454
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.4940C>T (p.Thr1647Ile) rs34271211 0.00909
NM_025074.7(FRAS1):c.1710C>T (p.Pro570=) rs17003124 0.00783
NM_025074.7(FRAS1):c.10598G>A (p.Arg3533Gln) rs115878217 0.00648
NM_025074.7(FRAS1):c.9806G>A (p.Arg3269Gln) rs61729366 0.00592
NM_025074.7(FRAS1):c.10312G>A (p.Val3438Met) rs34063631 0.00478
NM_025074.7(FRAS1):c.4877C>T (p.Ala1626Val) rs17003213 0.00468
NM_025074.7(FRAS1):c.8215G>A (p.Ala2739Thr) rs192476468 0.00426
NM_025074.7(FRAS1):c.10149C>T (p.Thr3383=) rs35321934 0.00379
NM_025074.7(FRAS1):c.10160T>C (p.Leu3387Pro) rs137982616 0.00365
NM_025074.7(FRAS1):c.776T>G (p.Leu259Arg) rs148509395 0.00356
NM_025074.7(FRAS1):c.5046C>G (p.Asp1682Glu) rs35219594 0.00344
NM_025074.7(FRAS1):c.6301C>T (p.His2101Tyr) rs183398121 0.00302
NM_025074.7(FRAS1):c.8832C>T (p.Ser2944=) rs114854941 0.00296
NM_025074.7(FRAS1):c.11907C>G (p.His3969Gln) rs140492803 0.00272
NM_025074.7(FRAS1):c.11724T>C (p.Ser3908=) rs151307846 0.00264
NM_025074.7(FRAS1):c.11718T>C (p.Ile3906=) rs142389362 0.00240
NM_025074.7(FRAS1):c.11605A>G (p.Ile3869Val) rs145035489 0.00236
NM_025074.7(FRAS1):c.10594A>G (p.Ile3532Val) rs144715071 0.00232
NM_025074.7(FRAS1):c.4958C>T (p.Pro1653Leu) rs6813102 0.00134
NM_025074.7(FRAS1):c.10539A>G (p.Thr3513=) rs199921300 0.00098
NM_025074.7(FRAS1):c.5725G>A (p.Val1909Ile) rs182652779 0.00049
NM_025074.7(FRAS1):c.6530T>C (p.Val2177Ala) rs76345011 0.00020
NM_025074.7(FRAS1):c.109-15del rs548267943
NM_025074.7(FRAS1):c.2060A>G (p.Asp687Gly) rs345513
NM_025074.7(FRAS1):c.380C>G (p.Pro127Arg) rs147709711
NM_025074.7(FRAS1):c.7029+9A>C rs188606284

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