Variant #0000293195 (NC_000003.11:g.132401603G>C, NM_153240.4:c.3756C>G (NPHP3))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.132401603G>C
DNA change (hg38) g.132682759G>C
Published as NPHP3(NM_153240.4):c.3756C>G (p.S1252R), NPHP3(NM_153240.5):c.3756C>G (p.S1252R)
ISCN -
DB-ID NPHP3_000003 See all 3 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) 0.00069 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UBA5 NM_024818.3 ?/. - c.*6233G>C r.(=) p.(=)
ACAD11 NM_032169.4 ?/. - c.-23008C>G r.(?) p.(=)
NPHP3 NM_153240.4 ?/. - c.3756C>G r.(?) p.(Ser1252Arg)
NPHP3-ACAD11 NR_037804.1 ?/. - n.3762C>G r.(?) -


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