ClinVar Miner

Submissions for variant NM_000094.4(COL7A1):c.4859G>A (p.Arg1620Gln)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pathology and Laboratory Medicine,Sinai Health System RCV001355646 SCV001550589 uncertain significance not provided no assertion criteria provided clinical testing The COL7A1 p.Arg1620Gln variant was not identified in the literature nor was it identified in ClinVar or LOVD 3.0. The variant was identified in dbSNP (ID: rs373682717) and Cosmic. The variant was identified in control databases in 23 of 280948 chromosomes at a frequency of 0.000082 (Genome Aggregation Database Feb 27, 2017). The variant was observed in the following populations: African in 13 of 24576 chromosomes (freq: 0.000529), European (Finnish) in 8 of 25060 chromosomes (freq: 0.000319), Other in 1 of 7170 chromosomes (freq: 0.00014) and European (non-Finnish) in 1 of 127980 chromosomes (freq: 0.000008), it was not observed in the Latino, Ashkenazi Jewish, East Asian, and South Asian populations. The p.Arg1620 residue is conserved in mammals but not in more distantly related organisms however four out of five computational analyses (SIFT, AlignGVGD, BLOSUM, MutationTaster) do not suggest a high likelihood of impact to the protein; this information is not predictive enough to rule out pathogenicity. The variant occurs outside of the splicing consensus sequence and in silico or computational prediction software programs (SpliceSiteFinder, MaxEntScan, NNSPLICE, GeneSplicer) do not predict a difference in splicing. In summary, based on the above information the clinical significance of this variant cannot be determined with certainty at this time. This variant is classified as a variant of uncertain significance.

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