ClinVar Miner

List of variants in gene DYRK1A reported as likely benign for DYRK1A-related intellectual disability syndrome

Included ClinVar conditions (2):
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Gene type:
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Total variants: 19
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HGVS dbSNP
NM_001347721.2(DYRK1A):c.1311C>T (p.Val437=) rs149417608
NM_001347721.2(DYRK1A):c.1800T>C (p.His600=) rs867610020
NM_001347721.2(DYRK1A):c.1818T>C (p.His606=) rs372827991
NM_001347721.2(DYRK1A):c.2049T>C (p.Phe683=) rs375130004
NM_001347721.2(DYRK1A):c.2085C>G (p.Val695=) rs372748919
NM_001347721.2(DYRK1A):c.234C>T (p.Asp78=) rs1049764
NM_001396.4(DYRK1A):c.1038C>G (p.Ser346=) rs1555985655
NM_001396.4(DYRK1A):c.11-9T>G rs1555976923
NM_001396.4(DYRK1A):c.1205C>G (p.Thr402Ser) rs777270510
NM_001396.4(DYRK1A):c.138A>T (p.Pro46=) rs1049759
NM_001396.4(DYRK1A):c.1602G>A (p.Gln534=) rs1555991440
NM_001396.4(DYRK1A):c.1635C>T (p.Ala545=) rs151236032
NM_001396.4(DYRK1A):c.1672-7C>T rs1198926046
NM_001396.4(DYRK1A):c.1762A>C (p.Thr588Pro) rs149948846
NM_001396.4(DYRK1A):c.1794G>A (p.Leu598=) rs1555994711
NM_001396.4(DYRK1A):c.2172T>C (p.Ala724=) rs1173777263
NM_001396.4(DYRK1A):c.354A>G (p.Arg118=) rs760666489
NM_001396.4(DYRK1A):c.360A>G (p.Gln120=) rs370463929
NM_001396.4(DYRK1A):c.375C>T (p.Asp125=) rs150200258

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