Variant #0000304440 (NC_000003.11:g.132427030C>T, NM_153240.4:c.1190G>A (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.132427030C>T
DNA change (hg38) g.132708186C>T
Published as NPHP3(NM_153240.4):c.1190G>A (p.R397H)
ISCN -
DB-ID NPHP3_000036
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) 0.00012 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UBA5 NM_024818.3 ?/. - c.*31660C>T r.(=) p.(=)
ACAD11 NM_032169.4 ?/. - c.-48435G>A r.(?) p.(=)
NPHP3 NM_153240.4 ?/. - c.1190G>A r.(?) p.(Arg397His)
NPHP3-ACAD11 NR_037804.1 ?/. - n.1294G>A r.(?) -


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