Variant #0000915020 (NC_000018.9:g.21114440C>A, NM_000271.4:c.3561G>T (NPC1))
| Chromosome |
18 |
| 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.21114440C>A |
| DNA change (hg38) |
- |
| Published as |
NPC1(NM_000271.4):c.3561G>T (p.A1187=), NPC1(NM_000271.5):c.3561G>T (p.A1187=, p.(Ala1187=)) |
| ISCN |
- |
| DB-ID |
NPC1_000019 See all 7 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) |
0.00262 View details |
| Owner |
VKGL-NL_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2023-01-11 15:44:22 +01:00 (CET) |
| Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
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