ClinVar Miner

Submissions for variant NM_003664.4(AP3B1):c.2915A>G (p.Asn972Ser) (rs139968311)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000547832 SCV000639574 benign Hermansky Pudlak syndrome 2 2017-11-28 criteria provided, single submitter clinical testing
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago RCV000547832 SCV000898523 uncertain significance Hermansky Pudlak syndrome 2 2018-05-02 criteria provided, single submitter clinical testing AP3B1 NM_003664.4 exon 25 p.Asn972Ser (c.2915A>G): This variant has not been reported in the literature but is present in 0.6% (163/24026) of African alleles, including 1 homozygote in the Genome Aggregation Database (http://gnomad.broadinstitute.org/rs139968311). This variant is present in ClinVar (Variation ID:464884). This variant amino acid Serine (Ser) is present in >40 species and is not well conserved among evolutionarily distant species; this suggests that this variant may not impact the protein. Additional computational prediction tools do not suggest an impact. In summary, data on this variant is insufficient for disease classification. Therefore, the clinical significance of this variant is uncertain.

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