Variant #0000508942 (NC_000002.11:g.110962532C>A, NM_000272.3:c.14G>T (NPHP1))

Chromosome 2
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.110962532C>A
DNA change (hg38) g.110204955C>A
Published as NPHP1(NM_000272.3):c.14G>T (p.R5L), NPHP1(NM_000272.5):c.14G>T (p.R5L)
ISCN -
DB-ID NPHP1_000066 See all 9 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) 0.00752 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NPHP1 NM_000272.3 -?/. - c.14G>T r.(?) p.(Arg5Leu)
NPHP1 NM_001128178.1 -?/. - c.14G>T r.(?) p.(Arg5Leu)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.