Variant #0000016890 (NC_000019.9:g.36336332C>A, NM_004646.3:c.1868G>T (NPHS1))
| Chromosome |
19 |
| Allele |
Unknown |
| 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.36336332C>A |
| DNA change (hg38) |
g.35845430C>A |
| Published as |
exon 14 nt1868(G>T): Cys623>Phe; c.G1868T: p.C623F |
| ISCN |
- |
| DB-ID |
NPHS1_000077 See all 6 reported entries |
| Variant remarks |
1 North American CNF family (com-het) and 1 English (com-het), 1 German (hom), 1 Spanish (com-het) and 1 Caucasian (het) CNF patient |
| Reference |
PubMed: Lenkkeri at al. 1999, PubMed: Koziell et al. 2002, PubMed: Schoeb et al. 2010, PubMed: Santin et al. 2009 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
0/93 CON |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
4.0E-5 View details |
| 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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