ClinVar Miner

List of variants in gene MAPT reported by Genome Diagnostics Laboratory, Amsterdam University Medical Center

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
Download table as spreadsheet
HGVS dbSNP
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.1326C>T (p.Pro442=)
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.1708G>A (p.Ala570Thr) rs63750612
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.2120T>G (p.Leu707Arg) rs63749855
NM_001377265.1(MAPT):c.220+18C>T rs75242405
NM_001377265.1(MAPT):c.220+2432G>A
NM_001377265.1(MAPT):c.220+2477C>G
NM_001377265.1(MAPT):c.220+2535A>G rs1800547
NM_001377265.1(MAPT):c.220+2538C>G rs368845248
NM_001377265.1(MAPT):c.2392C>T (p.Arg798Trp) rs63750424
NM_001377265.1(MAPT):c.830C>T (p.Pro277Leu) rs63750417
NM_001377265.1(MAPT):c.914A>G (p.Gln305Arg) rs63750072

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.