List of variants reported as likely benign for NIK deficiency

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Show significances as they were submitted (without aggregation into standard terms)
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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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