Variant #0000016829 (NC_000019.9:g.36342442C>G, NM_004646.3:c.191G>C (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.36342442C>G
DNA change (hg38) g.35851540C>G
Published as exon 2 nt191(G>C): Trp64>Ser
ISCN -
DB-ID NPHS1_000016
Variant remarks 1 Finnish CNF family (com-het)
Reference PubMed: Lenkkeri at al. 1999
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency 0/30 CON
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 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 19:04:32 +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 +?/+? 02 c.191G>C r.(191g>c) p.(Trp64Ser)


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