ClinVar Miner

List of variants in gene MAP3K14 reported as likely benign for NIK deficiency

Included ClinVar conditions (1):
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Gene type:
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Total variants: 15
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HGVS dbSNP
NM_003954.5(MAP3K14):c.1009C>T (p.Leu337=) rs374376396
NM_003954.5(MAP3K14):c.1103G>A (p.Arg368Gln) rs200062238
NM_003954.5(MAP3K14):c.1131C>T (p.Asn377=) rs750776653
NM_003954.5(MAP3K14):c.1455C>T (p.Gly485=) rs549438131
NM_003954.5(MAP3K14):c.1546G>A (p.Val516Ile) rs367938510
NM_003954.5(MAP3K14):c.1587C>T (p.His529=) rs562409633
NM_003954.5(MAP3K14):c.168G>A (p.Glu56=) rs530385135
NM_003954.5(MAP3K14):c.2290A>G (p.Thr764Ala) rs56302559
NM_003954.5(MAP3K14):c.2292C>T (p.Thr764=) rs746706058
NM_003954.5(MAP3K14):c.2820T>C (p.His940=) rs751517422
NM_003954.5(MAP3K14):c.416G>A (p.Arg139His) rs533327337
NM_003954.5(MAP3K14):c.538-4G>C rs534556740
NM_003954.5(MAP3K14):c.555C>T (p.Leu185=) rs191629489
NM_003954.5(MAP3K14):c.651A>G (p.Leu217=) rs766144092
NM_003954.5(MAP3K14):c.880A>C (p.Lys294Gln) rs113278485

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