ClinVar Miner

Submissions for variant NM_002529.4(NTRK1):c.1252-6C>G

gnomAD frequency: 0.00004  dbSNP: rs776728101
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV001101681 SCV001258308 uncertain significance Hereditary insensitivity to pain with anhidrosis 2018-01-13 criteria provided, single submitter clinical testing This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score, this variant could not be ruled out of causing disease and therefore its association with disease required further investigation. A literature search was performed for the gene, cDNA change, and amino acid change (if applicable). No publications were found based on this search. This variant was therefore classified as a variant of unknown significance for this disease.
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001101681 SCV001473818 likely benign Hereditary insensitivity to pain with anhidrosis 2020-05-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001101681 SCV002944907 likely benign Hereditary insensitivity to pain with anhidrosis 2024-01-10 criteria provided, single submitter clinical testing
Ambry Genetics RCV003363109 SCV004071819 uncertain significance Inborn genetic diseases 2023-06-20 criteria provided, single submitter clinical testing The c.1234-6C>G intronic alteration consists of a C to G substitution 6 nucleotides before coding exon 10 in the NTRK1 gene. Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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