List of variants in gene SPRED1 reported as uncertain significance for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_152594.3(SPRED1):c.587C>T (p.Thr196Ile)	rs147474792	0.00008
NM_152594.3(SPRED1):c.1289G>C (p.Gly430Ala)	rs749389617	0.00006
NM_152594.3(SPRED1):c.424-5A>G	rs752656697	0.00004
NM_152594.3(SPRED1):c.1202G>T (p.Cys401Phe)	rs779058019	0.00003
NM_152594.3(SPRED1):c.583-9G>T	rs1421813002	0.00003
NM_152594.3(SPRED1):c.1282C>T (p.Arg428Cys)	rs941091989	0.00002
NM_152594.3(SPRED1):c.182G>A (p.Arg61His)	rs750686148	0.00002
NM_152594.3(SPRED1):c.170A>G (p.Asp57Gly)	rs959758606	0.00001
NM_152594.3(SPRED1):c.353G>A (p.Arg118Lys)	rs373381933	0.00001
NM_152594.3(SPRED1):c.-12G>C	rs371200183
NM_152594.3(SPRED1):c.-12G>T	rs371200183
NM_152594.3(SPRED1):c.-22A>C	rs1057518143
NM_152594.3(SPRED1):c.1087A>G (p.Ile363Val)
NM_152594.3(SPRED1):c.1108C>T (p.Leu370Phe)	rs397517870
NM_152594.3(SPRED1):c.1112G>C (p.Cys371Ser)
NM_152594.3(SPRED1):c.1117G>C (p.Glu373Gln)
NM_152594.3(SPRED1):c.1163C>T (p.Ser388Phe)	rs1888487548
NM_152594.3(SPRED1):c.1231T>C (p.Ser411Pro)
NM_152594.3(SPRED1):c.1281_*4dup (p.His427_Ter445=)	rs1888490960
NM_152594.3(SPRED1):c.1304G>A (p.Cys435Tyr)
NM_152594.3(SPRED1):c.189G>C (p.Glu63Asp)	rs2140978555
NM_152594.3(SPRED1):c.221G>T (p.Cys74Phe)	rs1412213561
NM_152594.3(SPRED1):c.38G>A (p.Ser13Asn)	rs1057517922
NM_152594.3(SPRED1):c.424-4A>G	rs1057518328
NM_152594.3(SPRED1):c.502T>G (p.Tyr168Asp)	rs1566872960
NM_152594.3(SPRED1):c.582+16A>G	rs1895996789
NM_152594.3(SPRED1):c.808G>T (p.Asp270Tyr)
NM_152594.3(SPRED1):c.881A>T (p.Tyr294Phe)	rs886051105

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