ClinVar Miner

List of variants in gene MAPT reported as benign by Clinical Genetics, Academic Medical Center

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Total variants: 17
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NM_001377265.1(MAPT):c.-13A>G rs17650901
NM_001377265.1(MAPT):c.1078G>A (p.Asp360Asn) rs62063786
NM_001377265.1(MAPT):c.1080C>T (p.Asp360=) rs63750222
NM_001377265.1(MAPT):c.1091T>C (p.Val364Ala) rs62063787
NM_001377265.1(MAPT):c.1178C>T (p.Ser393Leu) rs73314997
NM_001377265.1(MAPT):c.1333C>T (p.Arg445Trp) rs17651549
NM_001377265.1(MAPT):c.1546T>C (p.Tyr516His) rs2258689
NM_001377265.1(MAPT):c.1564T>C (p.Ser522Pro) rs10445337
NM_001377265.1(MAPT):c.1704G>A (p.Pro568=) rs1052551
NM_001377265.1(MAPT):c.1732+2342T>C rs62063845
NM_001377265.1(MAPT):c.1857A>G (p.Ala619=) rs1052553
NM_001377265.1(MAPT):c.1941T>C (p.Asn647=) rs17652121
NM_001377265.1(MAPT):c.1986G>A (p.Pro662=) rs11568305
NM_001377265.1(MAPT):c.220+18C>T rs75242405
NM_001377265.1(MAPT):c.220+2535A>G rs1800547
NM_001377265.1(MAPT):c.830C>T (p.Pro277Leu) rs63750417
NM_001377265.1(MAPT):c.914A>G (p.Gln305Arg) rs63750072

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