ClinVar Miner

List of variants in gene TYK2 studied for not specified

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Total variants: 47
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HGVS dbSNP gnomAD frequency
NM_003331.5(TYK2):c.2908+31T>C rs280497 0.55677
NM_003331.5(TYK2):c.1669+7T>C rs280519 0.52527
NM_003331.5(TYK2):c.1477-6T>C rs280520 0.27974
NM_003331.5(TYK2):c.629+26T>C rs34725611 0.22818
NM_003331.5(TYK2):c.1084G>T (p.Val362Phe) rs2304256 0.22701
NM_003331.5(TYK2):c.1368-59C>T rs280521 0.17265
NM_003331.5(TYK2):c.1012-36C>T rs12720270 0.15757
NM_003331.5(TYK2):c.2311+11G>C rs12720299 0.11734
NM_003331.5(TYK2):c.516C>T (p.Thr172=) rs280523 0.10217
NM_003331.5(TYK2):c.2051T>G (p.Ile684Ser) rs12720356 0.06169
NM_003331.5(TYK2):c.1087G>A (p.Gly363Ser) rs2304255 0.05403
NM_003331.5(TYK2):c.2716-10T>G rs12720319 0.03021
NM_003331.5(TYK2):c.3310C>G (p.Pro1104Ala) rs34536443 0.02850
NM_003331.5(TYK2):c.2176-18C>G rs12720298 0.02818
NM_003331.5(TYK2):c.1848T>G (p.Pro616=) rs12720276 0.02503
NM_003331.5(TYK2):c.1953C>T (p.Ile651=) rs12720355 0.01009
NM_003331.5(TYK2):c.590G>A (p.Arg197His) rs12720263 0.00860
NM_003331.5(TYK2):c.942C>T (p.His314=) rs12720266 0.00844
NM_003331.5(TYK2):c.157G>A (p.Ala53Thr) rs55762744 0.00716
NM_003331.5(TYK2):c.-21+7T>G rs77948647 0.00645
NM_003331.5(TYK2):c.2783C>T (p.Ala928Val) rs35018800 0.00499
NM_003331.5(TYK2):c.3330G>A (p.Glu1110=) rs114073289 0.00353
NM_003331.5(TYK2):c.1960-15G>A rs12720277 0.00261
NM_003331.5(TYK2):c.3488A>G (p.Glu1163Gly) rs55886939 0.00226
NM_003331.5(TYK2):c.3201-8C>T rs2304252 0.00176
NM_003331.5(TYK2):c.513G>A (p.Ser171=) rs55988893 0.00051
NM_003331.5(TYK2):c.193+14G>A rs199931972 0.00041
NM_003331.5(TYK2):c.2670G>C (p.Thr890=) rs144332908 0.00026
NM_003331.5(TYK2):c.42C>T (p.Pro14=) rs543965548 0.00024
NM_003331.5(TYK2):c.639C>T (p.Asp213=) rs375654286 0.00016
NM_003331.5(TYK2):c.708C>T (p.Asn236=) rs372328362 0.00011
NM_003331.5(TYK2):c.2494C>T (p.Arg832Trp) rs144995884 0.00009
NM_003331.5(TYK2):c.2003C>T (p.Thr668Met) rs146430107 0.00008
NM_003331.5(TYK2):c.1011+20C>T rs747045647 0.00004
NM_003331.5(TYK2):c.2286G>A (p.Val762=) rs778089592 0.00004
NM_003331.5(TYK2):c.2646G>C (p.Pro882=) rs184567726 0.00003
NM_003331.5(TYK2):c.630-12G>A rs758598921 0.00003
NM_003331.5(TYK2):c.1669+10T>C rs536378862 0.00001
NM_003331.5(TYK2):c.1670-19A>G rs534465521 0.00001
NM_003331.5(TYK2):c.2617+13C>T rs770667639 0.00001
NM_003331.5(TYK2):c.588C>A (p.Leu196=) rs748702569 0.00001
NM_003331.5(TYK2):c.1011+12G>A rs377517686
NM_003331.5(TYK2):c.1774-4G>C rs280518
NM_003331.5(TYK2):c.2175+100GTTT[3] rs143429818
NM_003331.5(TYK2):c.2312-4C>G rs1057522650
NM_003331.5(TYK2):c.2371_2376del (p.Leu791_Ser792del) rs773966828
NM_003331.5(TYK2):c.465+135del rs34301809

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