ClinVar Miner

Submissions for variant NM_022081.6(HPS4):c.1640G>C (p.Cys547Ser)

gnomAD frequency: 0.00008  dbSNP: rs145674158
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001496663 SCV001701368 likely benign not provided 2024-05-12 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV002271657 SCV002555829 likely benign not specified 2022-06-10 criteria provided, single submitter clinical testing Variant summary: HPS4 c.1640G>C (p.Cys547Ser) results in a non-conservative amino acid change in the encoded protein sequence. Four of five in-silico tools predict a benign effect of the variant on protein function. The variant allele was found at a frequency of 0.00015 in 251344 control chromosomes (gnomAD), predominantly at a frequency of 0.0021 within the East Asian subpopulation in the gnomAD database. The observed variant frequency within East Asian control individuals in the gnomAD database is approximately 4 fold of the estimated maximal expected allele frequency for a pathogenic variant in HPS4 causing Hermansky-Pudlak Syndrome (0.00052), strongly suggesting that the variant is a benign polymorphism found primarily in populations of East Asian origin. To our knowledge, no occurrence of c.1640G>C in individuals affected with Hermansky-Pudlak Syndrome and no experimental evidence demonstrating its impact on protein function have been reported. One ClinVar submitter has assessed the variant since 2014: the variant was classified as likely benign. Based on the evidence outlined above, the variant was classified as likely benign.

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