ClinVar Miner

List of variants in gene DNM1 reported as likely benign by Ambry Genetics

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Gene type:
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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_004408.4(DNM1):c.747C>T (p.Thr249=) rs141651183 0.00086
NM_004408.4(DNM1):c.1707C>T (p.Asn569=) rs145318071 0.00039
NM_004408.4(DNM1):c.1437C>T (p.Ile479=) rs141788807 0.00036
NM_004408.4(DNM1):c.1386C>T (p.Thr462=) rs372666180 0.00020
NM_004408.4(DNM1):c.1586A>G (p.Asn529Ser) rs150040014 0.00019
NM_004408.4(DNM1):c.849+6C>T rs527412689 0.00013
NM_004408.4(DNM1):c.1200G>A (p.Thr400=) rs373198034 0.00009
NM_004408.4(DNM1):c.2541G>A (p.Ser847=) rs545142847 0.00007
NM_004408.4(DNM1):c.1161G>A (p.Glu387=) rs998519750 0.00002
NM_004408.4(DNM1):c.1617G>A (p.Lys539=) rs908450540 0.00002
NM_004408.4(DNM1):c.702G>A (p.Val234=) rs754094661 0.00002
NM_004408.4(DNM1):c.1116C>T (p.Phe372=) rs367584321 0.00001
NM_004408.4(DNM1):c.1356A>G (p.Leu452=) rs756954152 0.00001
NM_004408.4(DNM1):c.2113C>T (p.Leu705=) rs752228958 0.00001
NM_004408.4(DNM1):c.2178C>A (p.Asp726Glu) rs745835138 0.00001
NM_004408.4(DNM1):c.633C>T (p.Asp211=) rs1043525791 0.00001
NM_004408.4(DNM1):c.822G>A (p.Thr274=) rs765410948 0.00001
NM_004408.4(DNM1):c.1023G>A (p.Glu341=)
NM_004408.4(DNM1):c.1781+4C>A
NM_004408.4(DNM1):c.1899A>G (p.Lys633=)
NM_004408.4(DNM1):c.2232C>T (p.Asp744=) rs1315817571
NM_004408.4(DNM1):c.636G>A (p.Glu212=) rs766735683
NM_004408.4(DNM1):c.792T>A (p.Ser264=)

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