Variant #0000926668 (NC_000017.10:g.78157961G>T, NM_000199.3:c.*26290C>A (SGSH))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.78157961G>T |
| DNA change (hg38) |
- |
| Published as |
CARD14(NM_024110.4):c.599G>T (p.S200I) |
| ISCN |
- |
| DB-ID |
SGSH_000160 |
| 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) |
0.00141 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2023-04-16 21:50:28 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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