ClinVar Miner

Submissions for variant NM_001007792.1(NTRK1):c.264_269+3del (rs1571685736)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000809119 SCV000949260 likely pathogenic Hereditary insensitivity to pain with anhidrosis 2019-06-28 criteria provided, single submitter clinical testing This variant is a deletion of the genomic region encompassing part of exon 3 (c.354_359+3del) of the NTRK1 gene. It is expected to disrupt RNA splicing and likely results in an absent or disrupted protein product. This variant has been observed to be homozygous in an individual affected with hereditary sensory and autonomic neuropathy (PMID: 18322713). Loss-of-function variants in NTRK1 are known to be pathogenic (PMID: 10982191). In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic.
Inherited Neuropathy Consortium RCV000789508 SCV000928864 uncertain significance Charcot-Marie-Tooth disease no assertion criteria provided literature only

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