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 2 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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