ClinVar Miner

List of variants in gene TLK2 reported as uncertain significance for developmental disorder of mental health

Included ClinVar conditions (728):
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Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_006852.6(TLK2):c.1369-8C>T rs1413660720 0.00001
NM_006852.6(TLK2):c.1648A>T (p.Met550Leu) rs754747576 0.00001
NM_006852.6(TLK2):c.1015C>T (p.Arg339Trp) rs1567948262
NM_006852.6(TLK2):c.1016G>A (p.Arg339Gln) rs1567948287
NM_006852.6(TLK2):c.1273G>A (p.Glu425Lys) rs1567959483
NM_006852.6(TLK2):c.1310A>G (p.Asn437Ser)
NM_006852.6(TLK2):c.1456_1458del (p.His486del) rs2146902141
NM_006852.6(TLK2):c.1511T>G (p.Ile504Arg)
NM_006852.6(TLK2):c.1637G>A (p.Arg546Gln) rs2147165727
NM_006852.6(TLK2):c.163A>G (p.Lys55Glu) rs774263147
NM_006852.6(TLK2):c.1760T>G (p.Ile587Arg) rs2147185286
NM_006852.6(TLK2):c.1971G>C (p.Lys657Asn) rs1413696538
NM_006852.6(TLK2):c.2065_2067del (p.Thr689del) rs2147284765
NM_006852.6(TLK2):c.2092C>T (p.Arg698Ter) rs1555669421
NM_006852.6(TLK2):c.2119C>T (p.Arg707Cys)
NM_006852.6(TLK2):c.2170C>T (p.Arg724Ter) rs1568028078
NM_006852.6(TLK2):c.34C>T (p.Arg12Trp) rs796730233
NM_006852.6(TLK2):c.362C>T (p.Pro121Leu)
NM_006852.6(TLK2):c.416C>T (p.Ala139Val)
NM_006852.6(TLK2):c.732T>G (p.Asp244Glu)
NM_006852.6(TLK2):c.870G>A (p.Met290Ile) rs1451322597
NM_006852.6(TLK2):c.890G>A (p.Gly297Asp) rs1555639254

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