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 International |
Created by |
Y Yang |
Variant on transcripts
Screenings
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