Variant #0000097054 (NC_000020.10:g.49508756_49508759del, NM_015339.2:c.2496_2499del (ADNP))
| Chromosome |
20 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.49508756_49508759del |
| DNA change (hg38) |
g.50892219_50892222del |
| Published as |
2496_2499delTAAA |
| ISCN |
- |
| DB-ID |
ADNP_000004 See all 8 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
De novo |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Elisa Cappuyns |
| Database submission license |
No license selected |
| Created by |
Elisa Cappuyns |
| Date created |
2016-05-23 15:45:42 +02:00 (CEST) |
| Date last edited |
2024-10-23 12:40:41 +02:00 (CEST) |

Variant on transcripts
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