ClinVar Miner

List of variants in gene TYK2 reported as likely benign for not provided

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Gene type:
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Total variants: 55
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HGVS dbSNP gnomAD frequency
NM_003331.5(TYK2):c.1669+7T>C rs280519 0.52527
NM_003331.5(TYK2):c.2176-157A>C rs12979105 0.03702
NM_003331.5(TYK2):c.3027+66G>C rs12720359 0.02862
NM_003331.5(TYK2):c.3310C>G (p.Pro1104Ala) rs34536443 0.02850
NM_003331.5(TYK2):c.2908+178G>A rs12720358 0.01442
NM_003331.5(TYK2):c.2047+27C>T rs143978290 0.01433
NM_003331.5(TYK2):c.193+117C>T rs12720225 0.01183
NM_003331.5(TYK2):c.465+308G>A rs141536032 0.00992
NM_003331.5(TYK2):c.465+262C>T rs34923070 0.00907
NM_003331.5(TYK2):c.2467-270G>A rs12720306 0.00875
NM_003331.5(TYK2):c.2459C>A (p.Pro820His) rs34046749 0.00848
NM_003331.5(TYK2):c.194-288G>T rs115691830 0.00842
NM_003331.5(TYK2):c.1011+21G>A rs12720267 0.00840
NM_003331.5(TYK2):c.630-225A>G rs12720264 0.00839
NM_003331.5(TYK2):c.193+71G>A rs12720224 0.00830
NM_003331.5(TYK2):c.193+57G>A rs12720223 0.00822
NM_003331.5(TYK2):c.3201-81C>T rs149329233 0.00732
NM_003331.5(TYK2):c.1959+25G>A rs115703737 0.00725
NM_003331.5(TYK2):c.3200+23G>C rs12720360 0.00655
NM_003331.5(TYK2):c.2908+156C>A rs72563148 0.00581
NM_003331.5(TYK2):c.2909-152T>C rs12720321 0.00580
NM_003331.5(TYK2):c.2716-61G>T rs141407156 0.00578
NM_003331.5(TYK2):c.3318+196T>A rs187586005 0.00508
NM_003331.5(TYK2):c.2783C>T (p.Ala928Val) rs35018800 0.00499
NM_003331.5(TYK2):c.2716-55G>C rs56286467 0.00494
NM_003331.5(TYK2):c.2716-39T>C rs116502549 0.00491
NM_003331.5(TYK2):c.*199A>G rs12720335 0.00482
NM_003331.5(TYK2):c.2175+188G>A rs540171989 0.00410
NM_003331.5(TYK2):c.630-212G>A rs12720265 0.00372
NM_003331.5(TYK2):c.2716-128G>A rs12720318 0.00364
NM_003331.5(TYK2):c.3330G>A (p.Glu1110=) rs114073289 0.00353
NM_003331.5(TYK2):c.1012-204T>C rs12720269 0.00339
NM_003331.5(TYK2):c.1869C>T (p.Asp623=) rs140078545 0.00110
NM_003331.5(TYK2):c.2250C>T (p.Gly750=) rs138652649 0.00093
NM_003331.5(TYK2):c.44T>C (p.Val15Ala) rs144960992 0.00069
NM_003331.5(TYK2):c.513G>A (p.Ser171=) rs55988893 0.00051
NM_003331.5(TYK2):c.2176-156dup rs1483068125 0.00034
NM_003331.5(TYK2):c.648G>A (p.Pro216=) rs142642403 0.00030
NM_003331.5(TYK2):c.2670G>C (p.Thr890=) rs144332908 0.00026
NM_003331.5(TYK2):c.810C>T (p.Phe270=) rs56107150 0.00021
NM_003331.5(TYK2):c.1702C>T (p.Arg568Trp) rs569896082 0.00014
NM_003331.5(TYK2):c.3200+3G>A rs143533630 0.00011
NM_003331.5(TYK2):c.1959+9G>A rs756452186 0.00009
NM_003331.5(TYK2):c.1362C>G (p.Pro454=) rs374268170 0.00004
NM_003331.5(TYK2):c.1821C>G (p.Arg607=) rs773859320 0.00004
NM_003331.5(TYK2):c.2814C>G (p.Pro938=) rs763629813 0.00004
NM_003331.5(TYK2):c.353G>A (p.Arg118Gln) rs369530676 0.00002
NM_003331.5(TYK2):c.3147C>G (p.Pro1049=) rs747568389 0.00001
NM_003331.5(TYK2):c.193+184_193+203del rs1245905985
NM_003331.5(TYK2):c.3201-162_3201-147del rs12720324
NM_003331.5(TYK2):c.466-156_466-154del rs750662938
NM_003331.5(TYK2):c.466-172dup rs750662938
NM_003331.5(TYK2):c.844C>T (p.Leu282=) rs753449931
NM_003331.5(TYK2):c.903A>C (p.Thr301=) rs1599351475
NM_003331.5(TYK2):c.957A>G (p.Thr319=) rs1317857991

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