ClinVar Miner

List of variants in gene LMAN1 reported as uncertain significance for coagulation protein disease

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 34
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HGVS dbSNP
NM_005570.4(LMAN1):c.*1168C>T rs770166340
NM_005570.4(LMAN1):c.*1298A>G rs762134361
NM_005570.4(LMAN1):c.*1305A>G rs886054036
NM_005570.4(LMAN1):c.*1332C>G rs779423308
NM_005570.4(LMAN1):c.*1390T>G rs566011013
NM_005570.4(LMAN1):c.*1452_*1455del rs886054035
NM_005570.4(LMAN1):c.*1565C>T rs140930139
NM_005570.4(LMAN1):c.*1616A>G rs543483287
NM_005570.4(LMAN1):c.*164A>G rs41332251
NM_005570.4(LMAN1):c.*1970T>G rs886054034
NM_005570.4(LMAN1):c.*1988C>T rs886054033
NM_005570.4(LMAN1):c.*2044A>G rs191555835
NM_005570.4(LMAN1):c.*2259A>T rs886054032
NM_005570.4(LMAN1):c.*2602G>T rs886054031
NM_005570.4(LMAN1):c.*2650G>A rs886054030
NM_005570.4(LMAN1):c.*2893G>A rs143943495
NM_005570.4(LMAN1):c.*2923C>T rs561819154
NM_005570.4(LMAN1):c.*424T>G rs886054037
NM_005570.4(LMAN1):c.*48G>A rs148071519
NM_005570.4(LMAN1):c.*57G>A rs41355245
NM_005570.4(LMAN1):c.*939C>T rs149781610
NM_005570.4(LMAN1):c.-5C>T rs765835101
NM_005570.4(LMAN1):c.1050G>T (p.Arg350=) rs185875271
NM_005570.4(LMAN1):c.1221-4T>C rs200829791
NM_005570.4(LMAN1):c.1319A>G (p.Lys440Arg) rs147071939
NM_005570.4(LMAN1):c.1392G>A (p.Pro464=) rs149932943
NM_005570.4(LMAN1):c.214+7C>T rs2277728
NM_005570.4(LMAN1):c.27C>G (p.Leu9=) rs747955217
NM_005570.4(LMAN1):c.478-15T>C rs183354795
NM_005570.4(LMAN1):c.539+3A>G rs201868497
NM_005570.4(LMAN1):c.540T>G (p.Asn180Lys) rs886054038
NM_005570.4(LMAN1):c.663A>G (p.Thr221=) rs368261071
NM_005570.4(LMAN1):c.821C>T (p.Pro274Leu) rs41476148
NM_005570.4(LMAN1):c.846G>A (p.Ser282=) rs377676111

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