Variant #0000016933 (NC_000019.9:g.36333331T>A, NM_004646.3:c.2456A>T (NPHS1))

Chromosome 19
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.36333331T>A
DNA change (hg38) g.35842429T>A
Published as A>T Asp819Val
ISCN -
DB-ID NPHS1_000120 See all 3 reported entries
Variant remarks 1 Japanese CNF family (hom)
Reference PubMed: Aya 2000
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency 0/21 control individualss
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 2019-03-03 20:44:58 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NPHS1 NM_004646.3 +/+ 11 c.2456A>T r.(?) p.(Asp819Val)


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