Variant #0000727288 (NC_000019.9:g.36341962C>G, NM_004646.3:c.427G>C (NPHS1))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.36341962C>G
DNA change (hg38) -
Published as NPHS1(NM_004646.4):c.427G>C (p.(Glu143Gln))
ISCN -
DB-ID NPHS1_000218 See all 2 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) 8.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2025-11-01 13:22:20 +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 ?/. - c.427G>C r.(?) p.(Glu143Gln)
KIRREL2 NM_032123.5 ?/. - c.-6060C>G r.(?) p.(=)


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