ClinVar Miner

List of variants in gene MAPT reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 41
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001377265.1(MAPT):c.1891G>A (p.Ala631Thr) rs63750096 0.00085
NM_001377265.1(MAPT):c.889C>A (p.Arg297Ser) rs150983093 0.00038
NM_001377265.1(MAPT):c.1070C>T (p.Ser357Leu) rs199644237 0.00014
NM_001377265.1(MAPT):c.1567C>T (p.Arg523Ter) rs200099007 0.00011
NM_001377265.1(MAPT):c.1115C>T (p.Ala372Val) rs377402921 0.00010
NM_001377265.1(MAPT):c.601C>T (p.Pro201Ser) rs776821664 0.00004
NM_001377265.1(MAPT):c.898G>A (p.Asp300Asn) rs779635238 0.00004
NM_001377265.1(MAPT):c.1042T>C (p.Ser348Pro) rs753640366 0.00003
NM_001377265.1(MAPT):c.1998+33G>A rs759546274 0.00003
NM_001377265.1(MAPT):c.1884G>A (p.Pro628=) rs145897970 0.00002
NM_001377265.1(MAPT):c.25G>A (p.Glu9Lys) rs762595428 0.00002
NM_001377265.1(MAPT):c.1011G>C (p.Glu337Asp) rs1157103342 0.00001
NM_001377265.1(MAPT):c.1390G>A (p.Asp464Asn) rs768615863 0.00001
NM_001377265.1(MAPT):c.1516G>A (p.Val506Met) rs375359117 0.00001
NM_001377265.1(MAPT):c.2364G>A (p.Ser788=) rs377720312 0.00001
NM_001377265.1(MAPT):c.110G>T (p.Gly37Val) rs966689443
NM_001377265.1(MAPT):c.1156G>A (p.Val386Met) rs747178896
NM_001377265.1(MAPT):c.1160A>C (p.Gln387Pro)
NM_001377265.1(MAPT):c.1319G>A (p.Gly440Glu)
NM_001377265.1(MAPT):c.1321A>C (p.Lys441Gln) rs1598276822
NM_001377265.1(MAPT):c.1478G>A (p.Gly493Asp) rs1555710393
NM_001377265.1(MAPT):c.1622C>T (p.Thr541Met)
NM_001377265.1(MAPT):c.1732+2367C>A
NM_001377265.1(MAPT):c.1750G>A (p.Gly584Arg) rs1568303669
NM_001377265.1(MAPT):c.1762G>A (p.Gly588Ser) rs1400315970
NM_001377265.1(MAPT):c.1795G>A (p.Gly599Ser)
NM_001377265.1(MAPT):c.1837C>T (p.Arg613Trp)
NM_001377265.1(MAPT):c.1838G>A (p.Arg613Gln)
NM_001377265.1(MAPT):c.1918G>A (p.Val640Met) rs369217369
NM_001377265.1(MAPT):c.1998+8T>A
NM_001377265.1(MAPT):c.1999G>T (p.Val667Leu) rs1064797225
NM_001377265.1(MAPT):c.2090G>T (p.Ser697Ile) rs63751165
NM_001377265.1(MAPT):c.2302C>G (p.Leu768Val) rs1598425089
NM_001377265.1(MAPT):c.233G>T (p.Gly78Val) rs144397565
NM_001377265.1(MAPT):c.2404A>C (p.Asn802His)
NM_001377265.1(MAPT):c.2492A>G (p.Gln831Arg)
NM_001377265.1(MAPT):c.2495G>C (p.Gly832Ala) rs2146226506
NM_001377265.1(MAPT):c.761_762del (p.Glu254fs) rs748194611
NM_001377265.1(MAPT):c.775G>A (p.Ala259Thr)
NM_001377265.1(MAPT):c.965A>G (p.Gln322Arg)
NM_001377265.1(MAPT):c.998G>C (p.Gly333Ala)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.