Variant #0000858803 (NC_000003.11:g.132394747G>A, NM_153240.4:c.*6007C>T (NPHP3))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.132394747G>A
DNA change (hg38) -
Published as UBA5(NM_024818.3):c.1111G>A (p.(Ala371Thr)), UBA5(NM_024818.4):c.1111G>A (p.A371T), UBA5(NM_024818.5):c.1111G>A (p.A371T)
ISCN -
DB-ID UBA5_000014 See all 17 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) 0.0019 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UBA5 NM_024818.3 +/. - c.1111G>A r.(?) p.(Ala371Thr)
ACAD11 NM_032169.4 +/. - c.-16152C>T r.(?) p.(=)
NPHP3 NM_153240.4 +/. - c.*6007C>T r.(=) p.(=)
NPHP3-ACAD11 NR_037804.1 +/. - n.3995+6011C>T r.(?) -


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