List of variants reported as uncertain significance for Normophosphatemic familial tumoral calcinosis

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_017654.4(SAMD9):c.4558G>T (p.Glu1520Ter)	rs200178876	0.00004
NM_017654.4(SAMD9):c.3381C>A (p.Tyr1127Ter)	rs572380130	0.00003
NM_017654.4(SAMD9):c.460C>T (p.Gln154Ter)	rs767558735	0.00001
NM_017654.4(SAMD9):c.1507del (p.Glu503fs)
NM_017654.4(SAMD9):c.1800_1801del (p.Glu600fs)	rs375515095
NM_017654.4(SAMD9):c.2009del (p.Asn670fs)
NM_017654.4(SAMD9):c.2198T>C (p.Ile733Thr)	rs778749748
NM_017654.4(SAMD9):c.2509dup (p.Arg837fs)	rs1554337029
NM_017654.4(SAMD9):c.3505C>T (p.Gln1169Ter)	rs1554336918
NM_017654.4(SAMD9):c.4331AAC[1] (p.Gln1445del)	rs755666547
NM_017654.4(SAMD9):c.95del (p.His32fs)	rs1085307093

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