ClinVar Miner

Submissions for variant NM_007375.4(TARDBP):c.36C>T (p.Asn12=)

gnomAD frequency: 0.00008  dbSNP: rs565091566
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV001099682 SCV001256154 uncertain significance Amyotrophic lateral sclerosis type 10 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). No publications were found based on this search. Allele frequency data from public databases did not allow this variant to be ruled in or out of causing disease. Therefore, this variant is classified as a variant of unknown significance.
Invitae RCV002067757 SCV002439059 likely benign Amyotrophic lateral sclerosis type 10; TARDBP-related frontotemporal dementia 2022-04-12 criteria provided, single submitter clinical testing
Ambry Genetics RCV002348556 SCV002621883 likely benign Inborn genetic diseases 2019-11-06 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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