Variant #0000016844 (NC_000019.9:g.36341342G>A, NM_004646.3:c.532C>T (NPHS1))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.36341342G>A
DNA change (hg38) g.35850440G>A
Published as 532C>T: Q178X
ISCN -
DB-ID NPHS1_000031
Variant remarks CNF patients with non specified number and origin.
Reference PubMed: Beltcheva et al. 2001
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2012-12-10 17:38:49 +01:00 (CET)
Date last edited 2017-05-05 18:33:04 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NPHS1 NM_004646.3 +/+ 05 c.532C>T r.(532c>u) p.(Gln178*)


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