Variant #0000517965 (NC_000003.11:g.132409501A>G, NC_000003.11(NM_153240.4):c.2571-7T>C (NPHP3))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.132409501A>G
DNA change (hg38) g.132690657A>G
Published as NPHP3(NM_153240.4):c.2571-7T>C, NPHP3(NM_153240.5):c.2571-7T>C
ISCN -
DB-ID NPHP3_000023 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) 0.03045 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +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.*14131A>G r.(=) p.(=)
ACAD11 NM_032169.4 -/. - c.-30906T>C r.(?) p.(=)
NPHP3 NM_153240.4 -/. - c.2571-7T>C r.(=) p.(=)
NPHP3-ACAD11 NR_037804.1 -/. - n.2577-7T>C r.(?) -


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