Variant #0000858807 (NC_000003.11:g.132438579A>G, NM_153240.4:c.489T>C (NPHP3))

Chromosome 3
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.132438579A>G
DNA change (hg38) -
Published as NPHP3(NM_153240.4):c.489T>C (p.H163=)
ISCN -
DB-ID ACAD11_000060
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UBA5 NM_024818.3 -?/. - c.*43209A>G r.(=) p.(=)
ACAD11 NM_032169.4 -?/. - c.-59984T>C r.(?) p.(=)
NPHP3 NM_153240.4 -?/. - c.489T>C r.(?) p.(His163=)
NPHP3-ACAD11 NR_037804.1 -?/. - n.593T>C r.(?) -


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