Variant #0000222241 (NC_000005.9:g.74009341_74009344del, NM_000521.3:c.782_785del (HEXB))
| Chromosome |
5 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.74009341_74009344del |
| DNA change (hg38) |
g.74713516_74713519del |
| Published as |
782_785delCTTT |
| ISCN |
- |
| DB-ID |
HEXB_000012 |
| Variant remarks |
not in 200 control individuals |
| Reference |
Oller Ramirez, SAG2017, Cordoba |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
1/132 case chromosomes |
| 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 |
2017-10-24 10:29:06 +02:00 (CEST) |
| Date last edited |
2017-10-24 10:29:30 +02:00 (CEST) |

Variant on transcripts
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