Variant #0000003935 (NC_000017.10:g.44061036T>C, MAPT(NM_016835.4):c.866T>C)

Individual ID 00003935
Chromosome 17
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.44061036T>C
Reference Higgins JJ1, Adler RL, Loveless JM.(1999)
DB-ID MAPT_000042
Frequency -
Average frequency (gnomAD v.2.1.1) 0.14545 View details
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_016835.4 ./. 6 c.866T>C r.(?) p.(Val289Ala) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000003935 ? ? MAPT 1 Y Yang