Variant #0000001338 (NC_000017.10:g.44087769G>A, MAPT(NM_001123066.3):c.1920+1G>A)

Individual ID 00001338
Chromosome 17
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.44087769G>A
Reference Spillantini MG1, Murrell JR, Goedert M, Farlow MR, Klug A, Ghetti B.(1998)
DB-ID MAPT_000032
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
MAPT NM_001123066.3 ./. IVS10 c.1920+1G>A r.spl? p.? - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000001338 ? ? MAPT 1 Y Yang