Variant #0000000799 (NC_000022.10:g.24109646G>A, CHCHD10(NM_213720.1):c.176C>T)

Individual ID 00000799
Chromosome 22
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.24109646G>A
Reference Bannwarth S1, Ait-El-Mkadem S1, Chaussenot A1, Genin EC2, Lacas-Gervais S3, Fragaki K1, Berg-Alonso L2, Kageyama Y4, Serre V5, Moore DG6, (2014)
DB-ID CHCHD10_000001
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     
CHCHD10 NM_213720.1 ./. 2 c.176C>T r.(?) p.(Ser59Leu) 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     
0000000799 ? ? CHCHD10 1 Y Yang