Variant #0000850137 (NC_000003.11:g.132390931A>G, NM_153240.4:c.*9823T>C (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.132390931A>G
DNA change (hg38) -
Published as UBA5(NM_024818.4):c.722A>G (p.E241G)
ISCN -
DB-ID ACAD11_000056
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +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.722A>G r.(?) p.(Glu241Gly)
ACAD11 NM_032169.4 ?/. - c.-12336T>C r.(?) p.(=)
NPHP3 NM_153240.4 ?/. - c.*9823T>C r.(=) p.(=)
NPHP3-ACAD11 NR_037804.1 ?/. - n.3995+9827T>C r.(?) -


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