Variant #0000858805 (NC_000003.11:g.132405181T>C, NM_153240.4:c.3252A>G (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.132405181T>C
DNA change (hg38) -
Published as NPHP3(NM_153240.4):c.3252A>G (p.T1084=), NPHP3(NM_153240.5):c.3252A>G (p.T1084=)
ISCN -
DB-ID NPHP3_000010 See all 4 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) 0.00149 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.*9811T>C r.(=) p.(=)
ACAD11 NM_032169.4 -?/. - c.-26586A>G r.(?) p.(=)
NPHP3 NM_153240.4 -?/. - c.3252A>G r.(?) p.(Thr1084=)
NPHP3-ACAD11 NR_037804.1 -?/. - n.3258A>G r.(?) -


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