ClinVar Miner

List of variants in gene FRAS1 reported as benign by PreventionGenetics, part of Exact Sciences

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Total variants: 46
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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.5366+13T>G rs2170899 0.31001
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.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.6924C>T (p.Val2308=) rs13123710 0.05675
NM_025074.7(FRAS1):c.1769T>C (p.Met590Thr) rs35030041 0.01189
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.11855T>C (p.Val3952Ala) rs35379534 0.00945
NM_025074.7(FRAS1):c.10269G>T (p.Pro3423=) rs34806279 0.00927
NM_025074.7(FRAS1):c.3409G>A (p.Asp1137Asn) rs73828000 0.00832
NM_025074.7(FRAS1):c.8215G>A (p.Ala2739Thr) rs192476468 0.00426
NM_025074.7(FRAS1):c.12039A>G (p.Ter4013=) rs61734892 0.00322
NM_025074.7(FRAS1):c.806G>A (p.Arg269Gln) rs202231425 0.00313
NM_025074.7(FRAS1):c.11907C>G (p.His3969Gln) rs140492803 0.00272
NM_025074.7(FRAS1):c.9553G>A (p.Gly3185Arg) rs202095663 0.00230
NM_025074.7(FRAS1):c.201A>G (p.Gln67=) rs117876433 0.00210
NM_025074.7(FRAS1):c.7652A>G (p.Gln2551Arg) rs183712679 0.00169
NM_025074.7(FRAS1):c.641C>T (p.Pro214Leu) rs200053639 0.00108
NM_025074.7(FRAS1):c.9627C>T (p.Tyr3209=) rs377369857 0.00036
NM_025074.7(FRAS1):c.109-15del rs548267943
NM_025074.7(FRAS1):c.2060A>G (p.Asp687Gly) rs345513
NM_025074.7(FRAS1):c.7029+9A>C rs188606284

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