Variant #0000016831 (NC_000019.9:g.36342275G>C, NM_004646.3:c.286C>G (NPHS1))
| Chromosome |
19 |
| Allele |
Paternal (confirmed) |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.36342275G>C |
| DNA change (hg38) |
g.35851373G>C |
| Published as |
c.286C>G: p.L96V |
| ISCN |
- |
| DB-ID |
NPHS1_000018 |
| Variant remarks |
1 CNF patient (com-het) |
| Reference |
PubMed: Philippe et al. 2008 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
0/94 CON |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Anne Polvi |
| Date created |
2012-12-10 17:38:49 +01:00 (CET) |
| Date last edited |
2017-05-05 19:04:32 +02:00 (CEST) |

Variant on transcripts
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