List of variants in gene MAPT reported as benign for Frontotemporal dementia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 30

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HGVS	dbSNP	gnomAD frequency
NM_001377265.1(MAPT):c.1546T>C (p.Tyr516His)	rs2258689	0.21570
NM_001377265.1(MAPT):c.1857A>G (p.Ala619=)	rs1052553	0.14782
NM_001377265.1(MAPT):c.1941T>C (p.Asn647=)	rs17652121	0.14693
NM_001377265.1(MAPT):c.1091T>C (p.Val364Ala)	rs62063787	0.14671
NM_001377265.1(MAPT):c.830C>T (p.Pro277Leu)	rs63750417	0.14668
NM_001377265.1(MAPT):c.1078G>A (p.Asp360Asn)	rs62063786	0.14666
NM_001377265.1(MAPT):c.1564T>C (p.Ser522Pro)	rs10445337	0.14666
NM_001377265.1(MAPT):c.1732+2342T>C	rs62063845	0.14662
NM_001377265.1(MAPT):c.220+2535A>G	rs1800547	0.14618
NM_001377265.1(MAPT):c.220+18C>T	rs75242405	0.14617
NM_001377265.1(MAPT):c.1333C>T (p.Arg445Trp)	rs17651549	0.14348
NM_001377265.1(MAPT):c.1704G>A (p.Pro568=)	rs1052551	0.12440
NM_001377265.1(MAPT):c.-18+124C>G	rs3744456	0.12381
NM_001377265.1(MAPT):c.1080C>T (p.Asp360=)	rs63750222	0.10563
NM_001377265.1(MAPT):c.1178C>T (p.Ser393Leu)	rs73314997	0.05622
NM_001377265.1(MAPT):c.1986G>A (p.Pro662=)	rs11568305	0.03866
NM_001377265.1(MAPT):c.914A>G (p.Gln305Arg)	rs63750072	0.03830
NM_001377265.1(MAPT):c.1708G>A (p.Ala570Thr)	rs63750612	0.01528
NM_001377265.1(MAPT):c.862G>A (p.Gly288Arg)	rs76375268	0.01093
NM_001377265.1(MAPT):c.896T>G (p.Val299Gly)	rs141120474	0.00235
NM_001377265.1(MAPT):c.2091+29G>A	rs63751443	0.00213
NM_001377265.1(MAPT):c.1732+2364C>T	rs187760483	0.00195
NM_001377265.1(MAPT):c.117G>A (p.Thr39=)	rs63750529	0.00154
NM_001377265.1(MAPT):c.912C>G (p.Pro304=)	rs142327009	0.00112
NM_001377265.1(MAPT):c.643C>T (p.Pro215Ser)	rs151115928	0.00019
NM_001377265.1(MAPT):c.1732+2367C>G	rs267604921	0.00013
NM_001377265.1(MAPT):c.2406T>C (p.Asn802=)	rs115381139	0.00009
NM_001377265.1(MAPT):c.176C>T (p.Pro59Leu)	rs143138715	0.00006
NM_001377265.1(MAPT):c.1761C>T (p.Ser587=)
NM_001377265.1(MAPT):c.1974G>A (p.Leu658=)	rs373081497

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