Variant #0000003939 (NC_000017.10:g.44087741T>A, MAPT(NM_005910.5):c.888T>A)

Individual ID 00003939
Chromosome 17
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.44087741T>A
Reference Pastor P1, Pastor E, Carnero C, Vela R, GarcĂ­a T, Amer G, Tolosa E, Oliva R.(2001)
DB-ID MAPT_000013 See all 2 reported entries
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
MAPT NM_005910.5 ./. 9 c.888T>A r.(?) p.(Asn296Lys) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000003939 ? ? MAPT 1 Y Yang