ClinVar Miner

Submissions for variant NM_030760.5(S1PR5):c.440G>C (p.Ser147Thr)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV004863565 SCV005498738 uncertain significance not specified 2024-06-26 criteria provided, single submitter clinical testing The c.440G>C (p.S147T) alteration is located in exon 2 (coding exon 1) of the S1PR5 gene. This alteration results from a G to C substitution at nucleotide position 440, causing the serine (S) at amino acid position 147 to be replaced by a threonine (T). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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