Variant #0000036396 (NC_000019.9:g.13002736del, NM_000159.3:c.219del (GCDH))
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic (recessive) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.13002736del |
| DNA change (hg38) |
g.12891922del |
| Published as |
c.219delC |
| ISCN |
- |
| DB-ID |
GCDH_000066 See all 10 reported entries |
| Variant remarks |
Geographic origin: Germany |
| Reference |
PubMed: Zschocke 2000 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline/De novo (untested) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Svenja Wagner |
| Database submission license |
No license selected |
| Created by |
Svenja Wagner |
| Date created |
2014-05-13 12:24:41 +02:00 (CEST) |
| Date last edited |
2024-11-11 14:52:25 +01:00 (CET) |

Variant on transcripts
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