ClinVar Miner

List of variants in gene ST3GAL3 reported by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 47
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HGVS dbSNP gnomAD frequency
NM_006279.5(ST3GAL3):c.636C>T (p.Gly212=) rs12140044 0.00451
NM_006279.5(ST3GAL3):c.618C>T (p.Arg206=) rs115003742 0.00183
NM_006279.5(ST3GAL3):c.822A>G (p.Pro274=) rs199852949 0.00079
NM_006279.5(ST3GAL3):c.1014C>G (p.Thr338=) rs149000966 0.00070
NM_006279.5(ST3GAL3):c.118+36C>G rs149404491 0.00031
NM_006279.5(ST3GAL3):c.753G>A (p.Ser251=) rs187276382 0.00029
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.1075C>T (p.Leu359=) rs200457973 0.00017
NM_006279.5(ST3GAL3):c.400A>T (p.Asn134Tyr) rs201834329 0.00013
NM_006279.5(ST3GAL3):c.684C>T (p.Leu228=) rs376627212 0.00010
NM_006279.5(ST3GAL3):c.303G>T (p.Arg101=) rs200957732 0.00009
NM_006279.5(ST3GAL3):c.900T>C (p.Pro300=) rs563317319 0.00009
NM_006279.5(ST3GAL3):c.841G>A (p.Ala281Thr) rs371540962 0.00006
NM_006279.5(ST3GAL3):c.945C>T (p.Asp315=) rs748922857 0.00005
NM_006279.5(ST3GAL3):c.1070A>T (p.Glu357Val) rs141947405 0.00004
NM_006279.5(ST3GAL3):c.660C>T (p.Tyr220=) rs201204481 0.00004
NM_006279.5(ST3GAL3):c.81G>A (p.Ala27=) rs201489310 0.00004
NM_006279.5(ST3GAL3):c.1099G>A (p.Val367Ile) rs369157620 0.00003
NM_006279.5(ST3GAL3):c.711G>A (p.Lys237=) rs763616499 0.00003
NM_006279.5(ST3GAL3):c.1023G>A (p.Met341Ile) rs895326720 0.00002
NM_006279.5(ST3GAL3):c.630C>T (p.Pro210=) rs763641682 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.234C>T (p.Tyr78=) rs550614361 0.00001
NM_006279.5(ST3GAL3):c.637G>A (p.Ala213Thr) rs780493101 0.00001
NM_006279.5(ST3GAL3):c.781C>T (p.Arg261Ter) rs1195818093 0.00001
NM_006279.5(ST3GAL3):c.87G>A (p.Lys29=) rs138684243 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.144C>T (p.Ser48=) rs756428954
NM_006279.5(ST3GAL3):c.15A>G (p.Val5=)
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.442C>T (p.Leu148=) rs1570937203
NM_006279.5(ST3GAL3):c.633G>T (p.Glu211Asp)
NM_006279.5(ST3GAL3):c.651T>G (p.Pro217=)
NM_006279.5(ST3GAL3):c.664C>T (p.Arg222Cys)
NM_006279.5(ST3GAL3):c.727G>A (p.Val243Ile)
NM_006279.5(ST3GAL3):c.840C>T (p.Ala280=) rs752116461
NM_006279.5(ST3GAL3):c.886C>T (p.Arg296Trp)
NM_006279.5(ST3GAL3):c.912T>C (p.Ser304=) rs1557562991
NM_006279.5(ST3GAL3):c.959C>T (p.Ala320Val)
NM_006279.5(ST3GAL3):c.975C>G (p.Asp325Glu)

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