Variant #0000508032 (NC_000001.10:g.5933335C>T, NM_015102.4:c.3292G>A (NPHP4))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5933335C>T |
| DNA change (hg38) |
g.5873275C>T |
| Published as |
NPHP4(NM_015102.3):c.3292G>A (p.(Ala1098Thr)), NPHP4(NM_015102.4):c.3292G>A (p.A1098T), NPHP4(NM_015102.5):c.3292G>A (p.A1098T) |
| ISCN |
- |
| DB-ID |
NPHP4_000025 See all 5 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) |
0.00069 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
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