Variant #0000517947 (NC_000003.11:g.132384704G>A, NM_153240.4:c.*16050C>T (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.132384704G>A
DNA change (hg38) g.132665860G>A
Published as UBA5(NM_024818.4):c.199G>A (p.D67N)
ISCN -
DB-ID ACAD11_000005
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) 0.00018 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UBA5 NM_024818.3 -?/. - c.199G>A r.(?) p.(Asp67Asn)
ACAD11 NM_032169.4 -?/. - c.-6109C>T r.(?) p.(=)
NPHP3 NM_153240.4 -?/. - c.*16050C>T r.(=) p.(=)
NPHP3-ACAD11 NR_037804.1 -?/. - n.3995+16054C>T r.(?) -


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