ClinVar Miner

List of variants in gene DYRK1A reported as likely benign for not specified

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Total variants: 66
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HGVS dbSNP
NM_001347721.2(DYRK1A):c.1071+15G>A rs374505179
NM_001347721.2(DYRK1A):c.1072-19_1072-17del rs1384038532
NM_001347721.2(DYRK1A):c.1213-7C>T rs199867876
NM_001347721.2(DYRK1A):c.1339A>G (p.Ile447Val) rs1268200083
NM_001347721.2(DYRK1A):c.1519+14_1519+20dup rs1265719325
NM_001347721.2(DYRK1A):c.1539C>T (p.Ser513=) rs113110833
NM_001347721.2(DYRK1A):c.1644+101A>G rs188763724
NM_001347721.2(DYRK1A):c.1644+73C>A rs200322053
NM_001347721.2(DYRK1A):c.1644+86C>T rs184784885
NM_001347721.2(DYRK1A):c.1818T>C (p.His606=) rs372827991
NM_001347721.2(DYRK1A):c.2020C>T (p.Arg674Cys) rs201554841
NM_001347721.2(DYRK1A):c.2049T>C (p.Phe683=) rs375130004
NM_001347721.2(DYRK1A):c.208-28G>A rs552103257
NM_001347721.2(DYRK1A):c.208-38_208-35del rs1064794918
NM_001347721.2(DYRK1A):c.208-41del rs746060894
NM_001347721.2(DYRK1A):c.2085C>G (p.Val695=) rs372748919
NM_001347721.2(DYRK1A):c.2224A>T (p.Thr742Ser) rs147973077
NM_001347721.2(DYRK1A):c.234C>T (p.Asp78=) rs1049764
NM_001347721.2(DYRK1A):c.489+9A>G rs187936450
NM_001347721.2(DYRK1A):c.492T>C (p.Val164=) rs148892536
NM_001347721.2(DYRK1A):c.637+16A>G rs373230801
NM_001347721.2(DYRK1A):c.637+8_637+11del rs764954220
NM_001347721.2(DYRK1A):c.696G>T (p.Leu232=) rs549631808
NM_001347721.2(DYRK1A):c.925-19A>G rs78428152
NM_001347721.2(DYRK1A):c.925-8T>C rs199804785
NM_001396.4(DYRK1A):c.-37C>T rs755807124
NM_001396.4(DYRK1A):c.10+6T>G rs1057522660
NM_001396.4(DYRK1A):c.10+9A>G rs1555960038
NM_001396.4(DYRK1A):c.1002G>A (p.Leu334=) rs1057524118
NM_001396.4(DYRK1A):c.11-14_11-13del rs1064794556
NM_001396.4(DYRK1A):c.11-15C>G rs1057521693
NM_001396.4(DYRK1A):c.11-17C>T rs369277619
NM_001396.4(DYRK1A):c.1287G>A (p.Val429=) rs139043513
NM_001396.4(DYRK1A):c.1392C>A (p.Pro464=) rs745311187
NM_001396.4(DYRK1A):c.1428C>T (p.His476=) rs1057524542
NM_001396.4(DYRK1A):c.1542C>T (p.Ser514=) rs1555991138
NM_001396.4(DYRK1A):c.1547-9A>G rs1057524491
NM_001396.4(DYRK1A):c.1635C>T (p.Ala545=) rs151236032
NM_001396.4(DYRK1A):c.1671+13G>A rs752956372
NM_001396.4(DYRK1A):c.1671+15G>A rs1555991561
NM_001396.4(DYRK1A):c.1671+18T>C rs755097100
NM_001396.4(DYRK1A):c.1671+9G>A rs750741834
NM_001396.4(DYRK1A):c.1672-12C>G rs777693335
NM_001396.4(DYRK1A):c.1725A>C (p.Thr575=) rs375157979
NM_001396.4(DYRK1A):c.1920C>T (p.Ser640=) rs1057523331
NM_001396.4(DYRK1A):c.192A>G (p.Gln64=) rs1018001317
NM_001396.4(DYRK1A):c.1968A>G (p.Thr656=) rs773356976
NM_001396.4(DYRK1A):c.1986G>A (p.Thr662=) rs754773650
NM_001396.4(DYRK1A):c.1998G>C (p.Ser666=) rs755724183
NM_001396.4(DYRK1A):c.208-11G>A rs115030073
NM_001396.4(DYRK1A):c.208-6T>C rs1555979077
NM_001396.4(DYRK1A):c.208-7A>G rs201001986
NM_001396.4(DYRK1A):c.2109C>T (p.Thr703=) rs750035013
NM_001396.4(DYRK1A):c.2115C>T (p.Tyr705=) rs1555995350
NM_001396.4(DYRK1A):c.2215A>T (p.Met739Leu) rs201958918
NM_001396.4(DYRK1A):c.294T>G (p.Val98=) rs1049767
NM_001396.4(DYRK1A):c.328-17A>G rs200070302
NM_001396.4(DYRK1A):c.360A>G (p.Gln120=) rs370463929
NM_001396.4(DYRK1A):c.390G>A (p.Lys130=) rs991834315
NM_001396.4(DYRK1A):c.516+12G>A rs374459216
NM_001396.4(DYRK1A):c.664+10C>A rs775642525
NM_001396.4(DYRK1A):c.664+8A>C rs1555982713
NM_001396.4(DYRK1A):c.665-8T>G rs1555984066
NM_001396.4(DYRK1A):c.804G>A (p.Gln268=) rs1555984261
NM_001396.4(DYRK1A):c.822T>C (p.Leu274=) rs1057523364
NM_001396.4(DYRK1A):c.845G>A (p.Ser282Asn) rs758888181

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