Variant #0000863494 (NC_000014.8:g.21870169G>A, NM_001170629.1:c.4009C>T (CHD8))
| Chromosome |
14 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.21870169G>A |
| DNA change (hg38) |
g.21402010G>A |
| Published as |
CHD8(NM_001170629.1):c.4009C>T (p.(Arg1337*)), CHD8(NM_001170629.2):c.4009C>T (p.R1337*) |
| ISCN |
- |
| DB-ID |
CHD8_000015 See all 2 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) |
Retrieve |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2022-05-09 15:51:19 +02:00 (CEST) |
| Date last edited |
2022-08-11 14:25:59 +02:00 (CEST) |

Variant on transcripts
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