ClinVar Miner

List of variants in gene DHCR7 reported as uncertain significance for not provided

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Gene type:
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Total variants: 79
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HGVS dbSNP
NM_001360.2(DHCR7):c.1005G>A (p.Pro335=)
NM_001360.2(DHCR7):c.1011C>T (p.Ala337=) rs369382960
NM_001360.2(DHCR7):c.1012G>A (p.Val338Met) rs72954276
NM_001360.2(DHCR7):c.1087C>T (p.Arg363Cys)
NM_001360.2(DHCR7):c.1091C>T (p.Thr364Met) rs567600444
NM_001360.2(DHCR7):c.1099C>T (p.Arg367Cys) rs531038145
NM_001360.2(DHCR7):c.1152C>T (p.Ser384=)
NM_001360.2(DHCR7):c.1153G>A (p.Ala385Thr)
NM_001360.2(DHCR7):c.1155C>T (p.Ala385=)
NM_001360.2(DHCR7):c.1159G>A (p.Gly387Arg)
NM_001360.2(DHCR7):c.1168C>T (p.His390Tyr)
NM_001360.2(DHCR7):c.1203C>T (p.Gly401=)
NM_001360.2(DHCR7):c.1225G>A (p.Val409Ile) rs757861528
NM_001360.2(DHCR7):c.122C>T (p.Ala41Val) rs761265690
NM_001360.2(DHCR7):c.123G>A (p.Ala41=) rs376263149
NM_001360.2(DHCR7):c.1267G>A (p.Gly423Ser) rs902179640
NM_001360.2(DHCR7):c.1270G>A (p.Gly424Ser) rs368150818
NM_001360.2(DHCR7):c.1273G>A (p.Gly425Ser) rs760242
NM_001360.2(DHCR7):c.131T>C (p.Ile44Thr) rs142897396
NM_001360.2(DHCR7):c.1341C>T (p.Asp447=) rs139721775
NM_001360.2(DHCR7):c.1362G>A (p.Lys454=) rs147850435
NM_001360.2(DHCR7):c.1365C>T (p.Tyr455=) rs557097410
NM_001360.2(DHCR7):c.1366G>A (p.Gly456Ser)
NM_001360.2(DHCR7):c.1368C>T (p.Gly456=) rs144562471
NM_001360.2(DHCR7):c.1370G>A (p.Arg457Gln) rs886043122
NM_001360.2(DHCR7):c.1381C>T (p.Arg461Cys) rs199506852
NM_001360.2(DHCR7):c.1384T>C (p.Tyr462His) rs201270451
NM_001360.2(DHCR7):c.139C>T (p.Leu47=) rs140721259
NM_001360.2(DHCR7):c.1406G>A (p.Arg469His)
NM_001360.2(DHCR7):c.1406G>C (p.Arg469Pro) rs201150384
NM_001360.2(DHCR7):c.1410G>A (p.Leu470=) rs375993195
NM_001360.2(DHCR7):c.15G>A (p.Ser5=)
NM_001360.2(DHCR7):c.198C>T (p.Cys66=) rs775127532
NM_001360.2(DHCR7):c.199G>A (p.Ala67Thr) rs143999854
NM_001360.2(DHCR7):c.223A>T (p.Ile75Phe) rs370748173
NM_001360.2(DHCR7):c.233G>A (p.Gly78Glu) rs1565589472
NM_001360.2(DHCR7):c.241C>T (p.Arg81Trp) rs775735710
NM_001360.2(DHCR7):c.288C>T (p.Ala96=) rs745595242
NM_001360.2(DHCR7):c.28C>G (p.Pro10Ala) rs139166382
NM_001360.2(DHCR7):c.318C>T (p.Phe106=) rs1386646132
NM_001360.2(DHCR7):c.375C>T (p.Tyr125=) rs779401555
NM_001360.2(DHCR7):c.376G>A (p.Val126Ile) rs143587828
NM_001360.2(DHCR7):c.400G>T (p.Val134Leu) rs201466849
NM_001360.2(DHCR7):c.485C>T (p.Ala162Val) rs398123606
NM_001360.2(DHCR7):c.520T>G (p.Phe174Val) rs886044698
NM_001360.2(DHCR7):c.522C>T (p.Phe174=) rs140648594
NM_001360.2(DHCR7):c.571G>A (p.Val191Ile)
NM_001360.2(DHCR7):c.582C>T (p.Phe194=) rs150603941
NM_001360.2(DHCR7):c.58A>G (p.Asn20Asp) rs772572550
NM_001360.2(DHCR7):c.615C>T (p.Ser205=)
NM_001360.2(DHCR7):c.658A>C (p.Met220Leu) rs200659923
NM_001360.2(DHCR7):c.658A>T (p.Met220Leu) rs200659923
NM_001360.2(DHCR7):c.670G>A (p.Glu224Lys) rs373121544
NM_001360.2(DHCR7):c.69C>T (p.Thr23=) rs199798127
NM_001360.2(DHCR7):c.709C>T (p.Leu237=) rs755941916
NM_001360.2(DHCR7):c.70G>A (p.Ala24Thr)
NM_001360.2(DHCR7):c.719A>G (p.Asn240Ser) rs148609143
NM_001360.2(DHCR7):c.723G>T (p.Gly241=) rs369654651
NM_001360.2(DHCR7):c.729C>T (p.Pro243=) rs145284180
NM_001360.2(DHCR7):c.742T>C (p.Trp248Arg) rs886044494
NM_001360.2(DHCR7):c.771G>A (p.Ala257=)
NM_001360.2(DHCR7):c.778C>G (p.Arg260Gly) rs777617141
NM_001360.2(DHCR7):c.795T>C (p.His265=) rs1472363309
NM_001360.2(DHCR7):c.831+7G>A rs1318919210
NM_001360.2(DHCR7):c.840C>T (p.Tyr280=) rs148468879
NM_001360.2(DHCR7):c.84G>T (p.Gln28His) rs372855459
NM_001360.2(DHCR7):c.855C>T (p.Phe285=) rs781026169
NM_001360.2(DHCR7):c.862G>A (p.Glu288Lys) rs565893436
NM_001360.2(DHCR7):c.882C>T (p.Thr294=) rs748858240
NM_001360.2(DHCR7):c.89G>C (p.Gly30Ala) rs200334114
NM_001360.2(DHCR7):c.906C>T (p.Phe302=) rs80338858
NM_001360.2(DHCR7):c.91C>T (p.Arg31Cys) rs367585401
NM_001360.2(DHCR7):c.927C>A (p.Gly309=) rs149974099
NM_001360.2(DHCR7):c.92G>A (p.Arg31His) rs370307688
NM_001360.2(DHCR7):c.947A>G (p.Tyr316Cys)
NM_001360.2(DHCR7):c.957G>A (p.Thr319=)
NM_001360.2(DHCR7):c.963+7A>G
NM_001360.2(DHCR7):c.988G>A (p.Val330Met) rs139724817
NM_001360.2(DHCR7):c.99-5C>T rs372886043

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