ClinVar Miner

List of variants in gene CNNM4 reported as likely benign for Jalili syndrome

Included ClinVar conditions (1):
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Gene type:
ClinVar version:
Total variants: 10
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HGVS dbSNP
NM_020184.4(CNNM4):c.*1056C>T rs183039738
NM_020184.4(CNNM4):c.*1974C>T rs538676167
NM_020184.4(CNNM4):c.*459_*461TCC[6] rs202044868
NM_020184.4(CNNM4):c.*95T>C rs138947618
NM_020184.4(CNNM4):c.-14A>C rs545205153
NM_020184.4(CNNM4):c.1461C>T (p.Phe487=) rs147804021
NM_020184.4(CNNM4):c.1541T>C (p.Met514Thr) rs140192152
NM_020184.4(CNNM4):c.1851+9G>A rs185433115
NM_020184.4(CNNM4):c.399G>A (p.Val133=) rs34147094
NM_020184.4(CNNM4):c.434T>C (p.Met145Thr) rs148129550

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