Variant #0000082502 (NC_000015.9:g.34635241C>G, NM_018648.3:c.34G>C (NOP10))
| Chromosome |
15 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.34635241C>G |
| DNA change (hg38) |
g.34343040C>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
NOP10_000002 See all 3 reported entries |
| Variant remarks |
- |
| Reference |
PubMed: Walne 2007, Journal: Walne 2007 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
1/171 families |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.01001 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2015-10-26 19:29:19 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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