Variant #0000658904 (NC_000022.10:g.24110014C>T, CHCHD10(NM_213720.1):c.41+7G>A)
Chromosome |
22 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.24110014C>T |
DNA change (hg38) |
g.23767827C>T |
Published as |
CHCHD10(NM_001301339.1):c.41+7G>A, CHCHD10(NM_001301339.2):c.41+7G>A |
ISCN |
- |
DB-ID |
C22orf15_000005 See all 3 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.001 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2020-03-23 16:13:27 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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