ClinVar Miner

Submissions for variant NM_206933.3(USH2A):c.9258+1G>A (rs748810737)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000672669 SCV000797799 pathogenic Usher syndrome, type 2A; Retinitis pigmentosa 39 2018-02-13 criteria provided, single submitter clinical testing
Blueprint Genetics RCV001074509 SCV001240096 likely pathogenic Retinal dystrophy 2017-12-07 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV001091127 SCV001246992 pathogenic not provided 2018-07-01 criteria provided, single submitter clinical testing
Invitae RCV001091127 SCV001407857 pathogenic not provided 2020-10-06 criteria provided, single submitter clinical testing This sequence change affects a donor splice site in intron 46 of the USH2A gene. It is expected to disrupt RNA splicing and likely results in an absent or disrupted protein product. This variant is present in population databases (rs748810737, ExAC 0.002%). Disruption of this splice site has been observed in individual(s) with clinical features of USH2A-related conditions (PMID: 27460420, 31047384, 30902645, 28944237). ClinVar contains an entry for this variant (Variation ID: 265980). 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. Donor and acceptor splice site variants typically lead to a loss of protein function (PMID: 16199547), and loss-of-function variants in USH2A are known to be pathogenic (PMID: 10729113, 10909849, 20507924, 25649381). For these reasons, this variant has been classified as Pathogenic.
Bioscientia Institut fuer Medizinische Diagnostik GmbH,Sonic Healthcare RCV000256404 SCV000323138 likely pathogenic Usher syndrome, type 2A no assertion criteria provided clinical testing

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