List of variants in gene SLC34A3 reported as uncertain significance by Eurofins NTD LLC (GA)

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_001177316.2(SLC34A3):c.1149C>T (p.Ala383=)	rs199536442	0.00271
NM_001177316.2(SLC34A3):c.375C>T (p.Gly125=)	rs142873841	0.00108
NM_001177316.2(SLC34A3):c.1484G>C (p.Gly495Ala)	rs140869490	0.00072
NM_001177316.2(SLC34A3):c.1727G>T (p.Ser576Ile)	rs200090657	0.00064
NM_001177316.2(SLC34A3):c.1464T>C (p.Ala488=)	rs144666114	0.00054
NM_001177316.2(SLC34A3):c.1074G>A (p.Val358=)	rs146097023	0.00025
NM_001177316.2(SLC34A3):c.1473C>T (p.Tyr491=)	rs148095831	0.00022
NM_001177316.2(SLC34A3):c.698C>T (p.Ala233Val)	rs370826757	0.00006
NM_001177316.2(SLC34A3):c.1060G>A (p.Val354Met)	rs534880363	0.00005
NM_001177316.2(SLC34A3):c.1072G>A (p.Val358Met)	rs770332251	0.00005
NM_001177316.2(SLC34A3):c.987C>T (p.Ala329=)	rs372523225	0.00005
NM_001177316.2(SLC34A3):c.1164A>G (p.Ala388=)	rs762986714	0.00004
NM_001177316.2(SLC34A3):c.1198G>C (p.Val400Leu)	rs748862410	0.00004
NM_001177316.2(SLC34A3):c.882G>A (p.Pro294=)	rs370122685	0.00004
NM_001177316.2(SLC34A3):c.734C>T (p.Pro245Leu)	rs773260718	0.00003
NM_001177316.2(SLC34A3):c.978C>T (p.Ile326=)	rs886044633	0.00003
NM_001177316.2(SLC34A3):c.1703G>A (p.Arg568His)	rs1162579417	0.00002
NM_001177316.2(SLC34A3):c.383T>A (p.Val128Asp)	rs759826596	0.00002
NM_001177316.2(SLC34A3):c.449-3C>T	rs757092241	0.00002
NM_001177316.2(SLC34A3):c.423C>T (p.Ile141=)	rs748166039	0.00001
NM_001177316.2(SLC34A3):c.945C>T (p.Gly315=)	rs915920618	0.00001
NM_001177316.2(SLC34A3):c.305-8del	rs1283799215
NM_001177316.2(SLC34A3):c.448C>T (p.Leu150=)	rs200186549
NM_001177316.2(SLC34A3):c.533A>G (p.Gln178Arg)	rs1564417596
NM_001177316.2(SLC34A3):c.769A>G (p.Met257Val)	rs765193958
NM_001177316.2(SLC34A3):c.837G>A (p.Thr279=)	rs368153798

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