ClinVar Miner

List of variants in gene MAPT reported as benign for Grn-related frontotemporal lobar degeneration with Tdp43 inclusions

Included ClinVar conditions (12):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
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HGVS dbSNP
NM_016835.4(MAPT):c.1108C>T (p.Arg370Trp) rs17651549
NM_016835.4(MAPT):c.1339T>C (p.Ser447Pro) rs10445337
NM_016835.4(MAPT):c.1483G>A (p.Ala495Thr) rs63750612
NM_016835.4(MAPT):c.1507+2364C>T rs187760483
NM_016835.4(MAPT):c.1507+2367C>G rs267604921
NM_016835.4(MAPT):c.1749G>A (p.Leu583=) rs373081497
NM_016835.4(MAPT):c.1761G>A (p.Pro587=) rs11568305
NM_016835.4(MAPT):c.1866+29G>A rs63751443
NM_016835.4(MAPT):c.2181T>C (p.Asn727=) rs115381139
NM_016835.4(MAPT):c.418C>T (p.Pro140Ser) rs151115928
NM_016835.4(MAPT):c.637G>A (p.Gly213Arg) rs76375268
NM_016835.4(MAPT):c.687C>G (p.Pro229=) rs142327009
NM_016835.4(MAPT):c.689A>G (p.Gln230Arg) rs63750072

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