Variant #0000000108 (NC_000021.8:g.27264077A>G, APP(NM_000484.3):c.2168T>C)

Individual ID 00000108
Chromosome 21
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.27264077A>G
Reference Kwok JB1, Li QX, Hallupp M, Whyte S, Ames D, Beyreuther K, Masters CL, Schofield PR.(2000)
DB-ID APP_000017 See all 3 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     
APP NM_000484.3 ./. 17 c.2168T>C r.(?) p.(Leu723Pro) 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     
0000000108 ? ? APP 1 Y Yang