ClinVar Miner

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

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Gene type:
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Total variants: 29
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HGVS dbSNP
NM_001081.3(CUBN):c.10102A>G (p.Met3368Val) rs767333853
NM_001081.3(CUBN):c.10190_10191GA[1] (p.Asp3398fs) rs1564376600
NM_001081.3(CUBN):c.10431_10447del (p.Pro3477_Val3478insTer) rs1564374451
NM_001081.3(CUBN):c.10641G>A (p.Arg3547=) rs145909413
NM_001081.3(CUBN):c.1097G>C (p.Cys366Ser) rs1564518870
NM_001081.3(CUBN):c.1349G>A (p.Gly450Asp) rs146463364
NM_001081.3(CUBN):c.1450A>G (p.Ser484Gly) rs750735519
NM_001081.3(CUBN):c.2756A>G (p.His919Arg) rs148869805
NM_001081.3(CUBN):c.4069C>G (p.Pro1357Ala) rs780012075
NM_001081.3(CUBN):c.4268C>T (p.Thr1423Met) rs483352704
NM_001081.3(CUBN):c.4472A>C (p.Asp1491Ala) rs1064795523
NM_001081.3(CUBN):c.4669C>T (p.Leu1557Phe) rs140970422
NM_001081.3(CUBN):c.4720A>G (p.Met1574Val) rs1482983523
NM_001081.3(CUBN):c.4787G>A (p.Ser1596Asn) rs368081631
NM_001081.3(CUBN):c.5069C>T (p.Ala1690Val) rs141640975
NM_001081.3(CUBN):c.5084G>A (p.Arg1695His) rs145880377
NM_001081.3(CUBN):c.557A>G (p.Asn186Ser) rs1286216349
NM_001081.3(CUBN):c.5840C>A (p.Ser1947Tyr) rs147617753
NM_001081.3(CUBN):c.5856_5858delinsGGC (p.Gly1953Ala) rs1564434486
NM_001081.3(CUBN):c.6091A>G (p.Thr2031Ala) rs150392211
NM_001081.3(CUBN):c.6125-2A>G rs75386064
NM_001081.3(CUBN):c.6268A>G (p.Lys2090Glu) rs201374966
NM_001081.3(CUBN):c.7400A>G (p.Asn2467Ser) rs200197243
NM_001081.3(CUBN):c.8007dup (p.Val2670fs) rs1564414648
NM_001081.3(CUBN):c.8104del (p.Ser2702fs) rs1564412484
NM_001081.3(CUBN):c.8894T>C (p.Phe2965Ser) rs117620008
NM_001081.3(CUBN):c.8908C>T (p.Arg2970Cys) rs562374248
NM_001081.3(CUBN):c.9236+8A>G rs372673718
NM_001081.3(CUBN):c.9266_9268CCT[3] (p.Ser3090dup) rs1300066453

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