Variant #0000339397 (NC_000003.11:g.132405181T>C, NM_153240.4:c.3252A>G (NPHP3))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.132405181T>C
DNA change (hg38) g.132686337T>C
Published as NPHP3(NM_153240.4):c.3252A>G (p.T1084=), NPHP3(NM_153240.5):c.3252A>G (p.T1084=)
ISCN -
DB-ID NPHP3_000010 See all 4 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) 0.00149 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 2022-05-09 15:51:19 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UBA5 NM_024818.3 -/. - c.*9811T>C r.(=) p.(=)
ACAD11 NM_032169.4 -/. - c.-26586A>G r.(?) p.(=)
NPHP3 NM_153240.4 -/. - c.3252A>G r.(?) p.(Thr1084=)
NPHP3-ACAD11 NR_037804.1 -/. - n.3258A>G r.(?) -


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