ClinVar Miner

Submissions for variant NM_001059.3(TACR3):c.775C>T (p.Pro259Ser)

dbSNP: rs1057524840
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000429514 SCV000536590 uncertain significance not provided 2017-01-30 criteria provided, single submitter clinical testing The P259S variant has not been published as a pathogenic variant, nor has it been reported as a benign variant to our knowledge. However, the variant was not observed in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. P259S is a non-conservative amino acid substitution, which is likely to impact secondary protein structure as these residues differ in polarity, charge, size and/or other properties. This substitution occurs at a position that is conserved across species, and in silico analysis predicts this variant is probably damaging to the protein structure/function. Therefore, based on the currently available information, it is unclear whether this variant is a pathogenic variant or a rare benign variant.

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