Variant #0000517988 (NC_000003.11:g.132432016C>A, NM_153240.4:c.1072G>T (NPHP3))

Chromosome 3
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.132432016C>A
DNA change (hg38) g.132713172C>A
Published as -
ISCN -
DB-ID ACAD11_000028
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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UBA5 NM_024818.3 +/. - c.*36646C>A r.(=) p.(=)
ACAD11 NM_032169.4 +/. - c.-53421G>T r.(?) p.(=)
NPHP3 NM_153240.4 +/. - c.1072G>T r.(?) p.(Glu358Ter)
NPHP3-ACAD11 NR_037804.1 +/. - n.1176G>T r.(?) -


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