Variant #0000000208 (NC_000021.8:g.27264101A>G, APP(NM_000484.3):c.2144T>C)

Individual ID 00000208
Chromosome 21
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.27264101A>G
Reference Luedecke D1, Becktepe JS1, Lehmbeck JT1, Finckh U2, Yamamoto R2, Jahn H1, Boelmans K3.(2014)
DB-ID APP_000019 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
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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.2144T>C r.(?) p.(Val715Ala) 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     
0000000208 ? ? APP 1 Y Yang