ClinVar Miner

List of variants in gene ARMC5 reported as pathogenic for ACTH-independent Cushing syndrome

Included ClinVar conditions (9):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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HGVS dbSNP
ARMC5, 1-BP DEL, G
NM_001288767.2(ARMC5):c.1084C>T (p.Arg362Ter) rs369721476
NM_001288767.2(ARMC5):c.1379T>C (p.Leu460Pro) rs587777663
NM_001288767.2(ARMC5):c.1928T>C (p.Leu643Pro) rs587777661
NM_001288767.2(ARMC5):c.2062C>T (p.Arg688Trp) rs587777662
NM_001288767.2(ARMC5):c.2977C>T (p.Arg993Trp) rs587777659
NM_001288767.2(ARMC5):c.541C>T (p.Gln181Ter) rs587777660

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