ClinVar Miner

List of variants in gene MAPT reported as likely benign by GeneDx

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Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_001377265.1(MAPT):c.862G>A (p.Gly288Arg) rs76375268 0.00973
NM_001377265.1(MAPT):c.117G>A (p.Thr39=) rs63750529 0.00154
NM_001377265.1(MAPT):c.-17-215C>T
NM_001377265.1(MAPT):c.1351+21C>T
NM_001377265.1(MAPT):c.1351+48_1351+56del
NM_001377265.1(MAPT):c.1351+52C>T
NM_001377265.1(MAPT):c.1352-103C>T
NM_001377265.1(MAPT):c.1732+195C>A
NM_001377265.1(MAPT):c.1732+210dup
NM_001377265.1(MAPT):c.1733-31T>C
NM_001377265.1(MAPT):c.1998+147C>T
NM_001377265.1(MAPT):c.2092-192C>T
NM_001377265.1(MAPT):c.220+2202G>A
NM_001377265.1(MAPT):c.2286+109G>C
NM_001377265.1(MAPT):c.427G>T (p.Ala143Ser)
NM_001377265.1(MAPT):c.464G>A (p.Arg155His)
NM_001377265.1(MAPT):c.921C>G (p.Ser307=)

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