Variant #0000798926 (NC_000001.10:g.179520512del, NM_014625.2:c.948del (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.179520512del
DNA change (hg38) -
Published as NPHS2(NM_014625.2):c.948del (p.(Ala317LeufsTer31)), NPHS2(NM_014625.3):c.948delT (p.A317Lfs*31)
ISCN -
DB-ID NPHS2_000031 See all 16 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) 1.0E-5 View details
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 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NPHS2 NM_014625.2 +/. - c.948del r.(?) p.(Ala317Leufs*31)
AXDND1 NM_144696.4 +/. - c.3032-3135del r.(=) p.(=)


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