ClinVar Miner

Submissions for variant NM_014875.3(KIF14):c.3039G>A (p.Lys1013=)

gnomAD frequency: 0.00148  dbSNP: rs77213709
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000969928 SCV001117477 benign not provided 2024-11-19 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001819099 SCV002065493 benign not specified 2017-11-09 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000969928 SCV005287996 benign not provided criteria provided, single submitter not provided

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