ClinVar Miner

List of variants in gene combination DAAM2, MOCS1 reported as uncertain significance for amino acid or protein metabolism disease with epilepsy

Included ClinVar conditions (24):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
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HGVS dbSNP
NM_001358530.2(MOCS1):c.*1502A>G
NM_001358530.2(MOCS1):c.*1628C>T rs766403739
NM_001358530.2(MOCS1):c.*1660_*1663ATAG[3] rs112059918
NM_001358530.2(MOCS1):c.*1711G>A rs886061379
NM_001358530.2(MOCS1):c.*1752C>G
NM_001358530.2(MOCS1):c.*1808G>A
NM_001358530.2(MOCS1):c.*1832G>A
NM_001358530.2(MOCS1):c.*1835T>G
NM_001358530.2(MOCS1):c.*1857G>A rs193217053
NM_001358530.2(MOCS1):c.*1866_*1870dup rs370863199
NM_001358530.2(MOCS1):c.*1878G>A rs886061378
NM_001358530.2(MOCS1):c.*1884G>A
NM_001358530.2(MOCS1):c.*1942C>T rs764671362
NM_001358530.2(MOCS1):c.*1954G>A
NM_001358530.2(MOCS1):c.*2074A>G

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