ClinVar Miner

Submissions for variant NM_001114753.3(ENG):c.1258A>G (p.Met420Val)

gnomAD frequency: 0.00029  dbSNP: rs143724056
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV001168716 SCV001331326 uncertain significance Telangiectasia, hereditary hemorrhagic, type 1 2017-04-27 criteria provided, single submitter clinical testing This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). Publications were found based on this search. However, the evidence from the literature, in combination with allele frequency data from public databases where available, was not sufficient to rule this variant in or out of causing disease. Therefore, this variant is classified as a variant of unknown significance.
Invitae RCV001234384 SCV001407027 likely benign Hereditary hemorrhagic telangiectasia 2022-03-03 criteria provided, single submitter clinical testing

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