ClinVar Miner

List of variants in gene HSD3B7 reported as uncertain significance for not provided

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Total variants: 56
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HGVS dbSNP gnomAD frequency
NM_025193.4(HSD3B7):c.103C>G (p.Arg35Gly) rs150464212 0.00282
NM_025193.4(HSD3B7):c.234C>T (p.Ala78=) rs143699328 0.00104
NM_025193.4(HSD3B7):c.1090G>A (p.Ala364Thr) rs141997902 0.00054
NM_025193.4(HSD3B7):c.695-6C>T rs139152685 0.00048
NM_025193.4(HSD3B7):c.637G>A (p.Gly213Arg) rs143434186 0.00033
NM_025193.4(HSD3B7):c.608G>A (p.Arg203Lys) rs201349611 0.00030
NM_025193.4(HSD3B7):c.329G>A (p.Arg110Gln) rs141045776 0.00029
NM_025193.4(HSD3B7):c.695-5G>A rs201111173 0.00021
NM_025193.4(HSD3B7):c.1097G>C (p.Gly366Ala) rs147810715 0.00020
NM_025193.4(HSD3B7):c.997G>A (p.Val333Ile) rs143419053 0.00018
NM_025193.4(HSD3B7):c.40G>T (p.Val14Phe) rs374469295 0.00016
NM_025193.4(HSD3B7):c.1061G>A (p.Arg354Gln) rs757174407 0.00014
NM_025193.4(HSD3B7):c.226G>A (p.Ala76Thr) rs148706735 0.00014
NM_025193.4(HSD3B7):c.714C>T (p.His238=) rs147510106 0.00014
NM_025193.4(HSD3B7):c.7G>A (p.Asp3Asn) rs200555135 0.00011
NM_025193.4(HSD3B7):c.521A>G (p.Asn174Ser) rs750999061 0.00010
NM_025193.4(HSD3B7):c.*1C>T rs781013516 0.00009
NM_025193.4(HSD3B7):c.129C>G (p.Asp43Glu) rs371011295 0.00009
NM_025193.4(HSD3B7):c.558G>A (p.Thr186=) rs760192112 0.00008
NM_025193.4(HSD3B7):c.1047G>C (p.Ser349=) rs746926891 0.00007
NM_025193.4(HSD3B7):c.728G>A (p.Arg243Gln) rs769032830 0.00006
NM_025193.4(HSD3B7):c.859C>T (p.Arg287Cys) rs376499076 0.00005
NM_025193.4(HSD3B7):c.257C>T (p.Thr86Met) rs371576756 0.00004
NM_025193.4(HSD3B7):c.331A>C (p.Asn111His) rs369828425 0.00004
NM_025193.4(HSD3B7):c.498C>T (p.Ala166=) rs750739758 0.00004
NM_025193.4(HSD3B7):c.780C>T (p.Tyr260=) rs752601401 0.00004
NM_025193.4(HSD3B7):c.273C>T (p.Asp91=) rs200616143 0.00003
NM_025193.4(HSD3B7):c.323-3C>A rs1456158372 0.00003
NM_025193.4(HSD3B7):c.454G>A (p.Glu152Lys) rs774018498 0.00003
NM_025193.4(HSD3B7):c.837C>T (p.Cys279=) rs376286513 0.00003
NM_025193.4(HSD3B7):c.431+7_431+8insA rs1343784849 0.00002
NM_025193.4(HSD3B7):c.1088C>A (p.Ala363Asp) rs761166824 0.00001
NM_025193.4(HSD3B7):c.166+7G>T rs886043482 0.00001
NM_025193.4(HSD3B7):c.167-6G>A rs794727520 0.00001
NM_025193.4(HSD3B7):c.284G>A (p.Arg95Lys) rs756963815 0.00001
NM_025193.4(HSD3B7):c.365G>A (p.Arg122Gln) rs772927729 0.00001
NM_025193.4(HSD3B7):c.535C>T (p.Arg179Cys) rs137906271 0.00001
NM_025193.4(HSD3B7):c.576G>A (p.Thr192=) rs751904240 0.00001
NM_025193.4(HSD3B7):c.652C>T (p.Arg218Trp) rs775023023 0.00001
NM_025193.4(HSD3B7):c.671T>C (p.Val224Ala) rs750327663 0.00001
NM_025193.4(HSD3B7):c.838G>A (p.Gly280Arg) rs199637063 0.00001
NM_025193.4(HSD3B7):c.94C>T (p.Arg32Trp) rs775304061 0.00001
NM_025193.4(HSD3B7):c.-6-1_-6delinsTT rs1567369807
NM_025193.4(HSD3B7):c.226G>C (p.Ala76Pro) rs148706735
NM_025193.4(HSD3B7):c.263G>C (p.Gly88Ala) rs1567370766
NM_025193.4(HSD3B7):c.302T>C (p.Ile101Thr) rs1555492705
NM_025193.4(HSD3B7):c.328C>T (p.Arg110Trp)
NM_025193.4(HSD3B7):c.385A>G (p.Ser129Gly) rs1057524162
NM_025193.4(HSD3B7):c.388A>G (p.Met130Val) rs1567371284
NM_025193.4(HSD3B7):c.397G>A (p.Val133Met)
NM_025193.4(HSD3B7):c.542G>A (p.Gly181Glu)
NM_025193.4(HSD3B7):c.565C>T (p.Leu189Phe) rs1567371833
NM_025193.4(HSD3B7):c.586G>A (p.Gly196Ser) rs886044435
NM_025193.4(HSD3B7):c.727C>T (p.Arg243Trp) rs903191890
NM_025193.4(HSD3B7):c.844C>T (p.Arg282Trp)
NM_025193.4(HSD3B7):c.965A>G (p.Tyr322Cys)

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