Annotation Detail
Information
- Associated Genes
- MAPT
- Associated Variants
-
MAPT p.Leu658= (p.L658=)
(
ENST00000344290.10,
ENST00000574436.5,
ENST00000535772.6,
ENST00000446361.7,
ENST00000415613.6,
ENST00000262410.10,
ENST00000351559.10,
ENST00000431008.7,
ENST00000571987.5,
ENST00000420682.7,
ENST00000680674.1,
ENST00000334239.12 )
MAPT p.Leu658= (p.L658=) ( ENST00000262410.10, ENST00000334239.12, ENST00000344290.10, ENST00000351559.10, ENST00000415613.6, ENST00000420682.7, ENST00000431008.7, ENST00000446361.7, ENST00000535772.6, ENST00000571987.5, ENST00000574436.5, ENST00000680674.1 ) - Associated Disease
- MAPT-Related Spectrum Disorders
- Source Database
- ClinVar
- Description
- NM_001377265.1(MAPT):c.1972C>T (p.Leu658=) AND MAPT-Related Spectrum Disorders
- ClinVar Allele ID
- 877793
- ClinVar RefSeq Alternation Syntax
- NM_001377265.1:c.1972C>T
- ClinVar RefSeq Alternation Syntax
- NM_001377266.1:c.1774C>T
- ClinVar RefSeq Alternation Syntax
- NM_005910.6:c.796C>T
- ClinVar RefSeq Alternation Syntax
- NM_001123066.4:c.1801C>T
- ClinVar RefSeq Alternation Syntax
- NM_016834.5:c.622C>T
- ClinVar RefSeq Alternation Syntax
- NM_001203251.2:c.709C>T
- ClinVar RefSeq Alternation Syntax
- NM_001123067.4:c.709C>T
- ClinVar RefSeq Alternation Syntax
- NM_001203252.2:c.796C>T
- ClinVar RefSeq Alternation Syntax
- NM_001377268.1:c.622C>T
- ClinVar RefSeq Alternation Syntax
- NR_165166.1:n.720C>T
- ClinVar RefSeq Alternation Syntax
- NM_016835.5:c.1747C>T
- ClinVar RefSeq Alternation Syntax
- NM_016841.5:c.622C>T
- ClinVar RefSeq Alternation Syntax
- NM_001377267.1:c.709C>T
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2018-01-13
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001128502
- ClinVar Disease
- MAPT-Related Spectrum Disorders
- Observed Origin Sample
- germline
Drugs