Variant #0000850142 (NC_000003.11:g.132440961G>A, NM_153240.4:c.239C>T (NPHP3))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.132440961G>A
DNA change (hg38) -
Published as NPHP3(NM_153240.4):c.239C>T (p.S80L)
ISCN -
DB-ID ACAD11_000061
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UBA5 NM_024818.3 ?/. - c.*45591G>A r.(=) p.(=)
ACAD11 NM_032169.4 ?/. - c.-62366C>T r.(?) p.(=)
NPHP3 NM_153240.4 ?/. - c.239C>T r.(?) p.(Ser80Leu)
NPHP3-ACAD11 NR_037804.1 ?/. - n.343C>T r.(?) -


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