Variant #0000969272 (NC_000017.10:g.78188544dup, NM_000199.3:c.376dup (SGSH))
| Chromosome |
17 |
| 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.78188544dup |
| DNA change (hg38) |
- |
| Published as |
SGSH(NM_000199.4):c.376dupG (p.V126Gfs*10), SGSH(NM_000199.5):c.376dup (p.(Val126Glyfs*10)) |
| ISCN |
- |
| DB-ID |
SGSH_000080 See all 3 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_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2024-02-26 20:06:56 +01:00 (CET) |
| Date last edited |
2025-11-01 13:22:20 +01:00 (CET) |

Variant on transcripts
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