Variant #0000304442 (NC_000003.11:g.132441046C>T, NM_153240.4:c.154G>A (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.132441046C>T
DNA change (hg38) g.132722202C>T
Published as NPHP3(NM_153240.4):c.154G>A (p.A52T, p.(Ala52Thr)), NPHP3(NM_153240.5):c.154G>A (p.A52T)
ISCN -
DB-ID NPHP3_000001 See all 6 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) 0.01368 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.*45676C>T r.(=) p.(=)
ACAD11 NM_032169.4 -?/. - c.-62451G>A r.(?) p.(=)
NPHP3 NM_153240.4 -?/. - c.154G>A r.(?) p.(Ala52Thr)
NPHP3-ACAD11 NR_037804.1 -?/. - n.258G>A r.(?) -


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