Variant #0000517985 (NC_000003.11:g.132427063T>C, NM_153240.4:c.1157A>G (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.132427063T>C
DNA change (hg38) g.132708219T>C
Published as NPHP3(NM_153240.4):c.1157A>G (p.N386S), NPHP3(NM_153240.5):c.1157A>G (p.N386S)
ISCN -
DB-ID ACAD11_000025 See all 6 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) 0.00187 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.*31693T>C r.(=) p.(=)
ACAD11 NM_032169.4 -?/. - c.-48468A>G r.(?) p.(=)
NPHP3 NM_153240.4 -?/. - c.1157A>G r.(?) p.(Asn386Ser)
NPHP3-ACAD11 NR_037804.1 -?/. - n.1261A>G r.(?) -


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