ClinVar Miner

List of variants in gene ST3GAL3 reported as uncertain significance by Ambry Genetics

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Gene type:
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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_006279.5(ST3GAL3):c.118+36C>G rs149404491 0.00031
NM_006279.5(ST3GAL3):c.1079G>A (p.Arg360Gln) rs553120567 0.00027
NM_006279.5(ST3GAL3):c.362G>A (p.Arg121Gln) rs201287443 0.00027
NM_006279.5(ST3GAL3):c.400A>T (p.Asn134Tyr) rs201834329 0.00013
NM_006279.5(ST3GAL3):c.841G>A (p.Ala281Thr) rs371540962 0.00006
NM_006279.5(ST3GAL3):c.1070A>T (p.Glu357Val) rs141947405 0.00004
NM_006279.5(ST3GAL3):c.1099G>A (p.Val367Ile) rs369157620 0.00003
NM_006279.5(ST3GAL3):c.1023G>A (p.Met341Ile) rs895326720 0.00002
NM_006279.5(ST3GAL3):c.647G>A (p.Arg216Gln) rs368686769 0.00002
NM_006279.5(ST3GAL3):c.1015G>A (p.Val339Ile) rs767586606 0.00001
NM_006279.5(ST3GAL3):c.1097G>A (p.Arg366His) rs572958701 0.00001
NM_006279.5(ST3GAL3):c.637G>A (p.Ala213Thr) rs780493101 0.00001
NM_006279.5(ST3GAL3):c.946G>A (p.Glu316Lys) rs770661277 0.00001
NM_006279.5(ST3GAL3):c.989A>G (p.Asn330Ser) rs370499935 0.00001
NM_006279.5(ST3GAL3):c.118A>G (p.Asn40Asp)
NM_006279.5(ST3GAL3):c.173A>G (p.Asp58Gly)
NM_006279.5(ST3GAL3):c.25A>C (p.Asn9His)
NM_006279.5(ST3GAL3):c.343C>T (p.Arg115Cys) rs948699026
NM_006279.5(ST3GAL3):c.633G>T (p.Glu211Asp)
NM_006279.5(ST3GAL3):c.664C>T (p.Arg222Cys)
NM_006279.5(ST3GAL3):c.727G>A (p.Val243Ile)
NM_006279.5(ST3GAL3):c.886C>T (p.Arg296Trp)
NM_006279.5(ST3GAL3):c.959C>T (p.Ala320Val)
NM_006279.5(ST3GAL3):c.975C>G (p.Asp325Glu)

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