ClinVar Miner

Submissions for variant NM_002968.3(SALL1):c.1514A>G (p.His505Arg) (rs776094507)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Johns Hopkins Genomics,Johns Hopkins University RCV000855402 SCV000998463 uncertain significance Townes-Brocks syndrome 1 2019-08-04 criteria provided, single submitter clinical testing This SALL1 variant is absent from large population datasets and has not been reported in the literature, to our knowledge. Two bioinformatic tools queried predict that this substitution would be probably damaging, and the histidine residue at this position is evolutionarily conserved across all species assessed. Bioinformatic analysis predicts that this missense variant would not affect normal exon 2 splicing, although this has not been confirmed experimentally to our knowledge. Due to the presence of this variant in the proband's assumed unaffected father in addition to the lack of previously reported disease associated missense variation in SALL1, the clinical significance of c.1514A>G is uncertain at this time.

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