ClinVar Miner

Submissions for variant NM_003954.5(MAP3K14):c.411G>C (p.Lys137Asn)

dbSNP: rs922237736
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000799642 SCV000939315 uncertain significance NIK deficiency 2022-08-23 criteria provided, single submitter clinical testing This sequence change replaces lysine, which is basic and polar, with asparagine, which is neutral and polar, at codon 137 of the MAP3K14 protein (p.Lys137Asn). This variant is present in population databases (no rsID available, gnomAD 0.0009%). This variant has not been reported in the literature in individuals affected with MAP3K14-related conditions. ClinVar contains an entry for this variant (Variation ID: 645542). In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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