Variant #0000016834 (NC_000019.9:g.36342241G>A, NM_004646.3:c.320C>T (NPHS1))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.36342241G>A
DNA change (hg38) g.35851339G>A
Published as c.C320T: p.A107V
ISCN -
DB-ID NPHS1_000021
Variant remarks 2 Indian CNF patients (1 com-het and 1 het)
Reference PubMed: Schoeb et al. 2010
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency 0/93 CON
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Anne Polvi
Database submission license No license selected
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 ?/? 03 c.320C>T r.(320c>u) p.(Ala107Val)


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