Variant #0000798929 (NC_000001.10:g.179528842A>G, NM_014625.2:c.506T>C (NPHS2))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.179528842A>G
DNA change (hg38) -
Published as NPHS2(NM_014625.3):c.506T>C (p.L169P)
ISCN -
DB-ID NPHS2_000106 See all 15 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NPHS2 NM_014625.2 +/. - c.506T>C r.(?) p.(Leu169Pro)
AXDND1 NM_144696.4 +/. - c.*5188A>G r.(=) p.(=)


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