Variant #0000786109 (NC_000003.11:g.120371490C>G, NM_000187.3:c.291G>C (HGD))
| Chromosome |
3 |
| 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.120371490C>G |
| DNA change (hg38) |
g.120652643C>G |
| Published as |
W97C |
| ISCN |
- |
| DB-ID |
HGD_000177 |
| Variant remarks |
- |
| Reference |
Ascher (2019) - data and classification copied from HGD mutations database |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2021-05-21 10:09:09 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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