Variant #0000016836 (NC_000019.9:g.36341921G>C, NM_004646.3:c.468C>G (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.36341921G>C
DNA change (hg38) g.35851019G>C
Published as 468C>G: Y156X
ISCN -
DB-ID NPHS1_000023 See all 3 reported entries
Variant remarks CNF patients with non specified number and origin.
Reference PubMed: Beltcheva et al. 2001, PubMed: Philippe et al. 2008
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
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 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 +/+ 04 c.468C>G r.(468c>g) p.(Tyr156*)


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