Annotation Detail
Information
- Associated Genes
- MAPT
- Associated Variants
-
MAPT p.Leu707Arg (p.L707R)
(
ENST00000262410.10,
ENST00000446361.7,
ENST00000415613.6,
ENST00000535772.6,
ENST00000574436.5,
ENST00000344290.10,
ENST00000680674.1,
ENST00000420682.7,
ENST00000334239.12,
ENST00000431008.7,
ENST00000571987.5,
ENST00000351559.10 )
MAPT p.Leu707Arg (p.L707R) ( 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
- not provided
- Source Database
- ClinVar
- Description
- NM_001377265.1(MAPT):c.2120T>G (p.Leu707Arg) AND not provided
- ClinVar Allele ID
- 104118
- ClinVar RefSeq Alternation Syntax
- NM_001377268.1:c.677T>G
- ClinVar RefSeq Alternation Syntax
- NM_001123067.4:c.857T>G
- ClinVar RefSeq Alternation Syntax
- NM_005910.6:c.944T>G
- ClinVar RefSeq Alternation Syntax
- NM_016835.5:c.1895T>G
- ClinVar RefSeq Alternation Syntax
- NM_016834.5:c.770T>G
- ClinVar RefSeq Alternation Syntax
- NM_001377265.1:c.2120T>G
- ClinVar RefSeq Alternation Syntax
- NM_016841.5:c.677T>G
- ClinVar RefSeq Alternation Syntax
- NR_165166.1:n.775T>G
- ClinVar RefSeq Alternation Syntax
- NM_001203251.2:c.764T>G
- ClinVar RefSeq Alternation Syntax
- NM_001377266.1:c.1829T>G
- ClinVar RefSeq Alternation Syntax
- NM_001377267.1:c.764T>G
- ClinVar RefSeq Alternation Syntax
- NM_001203252.2:c.851T>G
- ClinVar RefSeq Alternation Syntax
- NM_001123066.4:c.1949T>G
- Clinical Significance Description
- Pathogenic
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000084541
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
- Observed Origin Sample
- not provided
Drugs