Genomic variant #0000016832

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.36342248C>T
DNA change (hg38) g.35851346C>T
Published as 313G>A: D105N
ISCN -
DB-ID NPHS1_000019
Variant remarks 2 Japanese CNF patients (com-het)
Reference PubMed: Sako et al. 2005
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency 0/200 JAP CON
Re-site -
VIP -
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Anne Polvi




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
NPHS1 NM_004646.3 +?/+? 03 c.313G>A - r.(313g>a) p.(Asp105Asn)