Variant #0000801001 (NC_000003.11:g.132432050T>C, NM_153240.4:c.1038A>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.132432050T>C
DNA change (hg38) -
Published as NPHP3(NM_153240.5):c.1038A>G (p.E346=)
ISCN -
DB-ID NPHP3_000068
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UBA5 NM_024818.3 -?/. - c.*36680T>C r.(=) p.(=)
ACAD11 NM_032169.4 -?/. - c.-53455A>G r.(?) p.(=)
NPHP3 NM_153240.4 -?/. - c.1038A>G r.(?) p.(Glu346=)
NPHP3-ACAD11 NR_037804.1 -?/. - n.1142A>G r.(?) -


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