Variant #0000342683 (NC_000001.10:g.6007259G>A, NM_015102.4:c.1024C>T (NPHP4))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.6007259G>A
DNA change (hg38) g.5947199G>A
Published as NPHP4(NM_015102.3):c.1024C>T (p.(Arg342Cys)), NPHP4(NM_015102.4):c.1024C>T (p.R342C), NPHP4(NM_015102.5):c.1024C>T (p.R342C)
ISCN -
DB-ID NPHP4_000081 See all 6 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) 0.00168 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.1024C>T r.(?) p.(Arg342Cys)


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