Variant #0000975586 (NC_000003.11:g.132441143C>G, NM_153240.4:c.57G>C (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.132441143C>G
DNA change (hg38) -
Published as NPHP3(NM_153240.4):c.57G>C (p.T19=), NPHP3(NM_153240.5):c.57G>C (p.(Thr19=))
ISCN -
DB-ID ACAD11_000032 See all 2 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) 0.01582 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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.*45773C>G r.(=) p.(=)
ACAD11 NM_032169.4 -?/. - c.-62548G>C r.(?) p.(=)
NPHP3 NM_153240.4 -?/. - c.57G>C r.(?) p.(Thr19=)
NPHP3-ACAD11 NR_037804.1 -?/. - n.161G>C r.(?) -


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