ClinVar Miner

Submissions for variant NM_002968.2(SALL1):c.3584G>A (p.Arg1195Gln) (rs1030315086)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000696783 SCV000825361 uncertain significance Townes syndrome 2018-08-02 criteria provided, single submitter clinical testing This sequence change replaces arginine with glutamine at codon 1195 of the SALL1 protein (p.Arg1195Gln). The arginine residue is highly conserved and there is a small physicochemical difference between arginine and glutamine. This variant is not present in population databases (ExAC no frequency). Family studies have indicated that an individual with bilateral congenital profound hearing loss and asymmetric kidneys inherited this variant from an unaffected parent, which suggests that this variant is not likely a primary cause of disease. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C0"). In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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