Variant #0000508032 (NC_000001.10:g.5933335C>T, NM_015102.4:c.3292G>A (NPHP4))

Chromosome 1
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.5933335C>T
DNA change (hg38) g.5873275C>T
Published as NPHP4(NM_015102.3):c.3292G>A (p.(Ala1098Thr)), NPHP4(NM_015102.4):c.3292G>A (p.A1098T), NPHP4(NM_015102.5):c.3292G>A (p.A1098T)
ISCN -
DB-ID NPHP4_000025 See all 5 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) 0.00069 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NPHP4 NM_015102.4 ?/. - c.3292G>A r.(?) p.(Ala1098Thr)


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