ClinVar Miner

Submissions for variant NM_000368.4(TSC1):c.1030delG

dbSNP: rs118203486
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001380785 SCV001578948 pathogenic Tuberous sclerosis 1 2020-10-01 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. Loss-of-function variants in TSC1 are known to be pathogenic (PMID: 10227394, 17304050). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site, but this prediction has not been confirmed by published transcriptional studies. This variant has not been reported in the literature in individuals with TSC1-related conditions. ClinVar contains an entry for this variant (Variation ID: 48733). This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Ala344Leufs*12) in the TSC1 gene. It is expected to result in an absent or disrupted protein product.
Tuberous sclerosis database (TSC1) RCV000041980 SCV000065759 not provided Tuberous sclerosis syndrome no assertion provided curation

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