Variant #0000801002 (NC_000003.11:g.132435639G>T, NM_153240.4:c.785C>A (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.132435639G>T
DNA change (hg38) -
Published as NPHP3(NM_153240.4):c.785C>A (p.S262Y)
ISCN -
DB-ID NPHP3_000069
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 2021-09-17 14:40:49 +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.*40269G>T r.(=) p.(=)
ACAD11 NM_032169.4 ?/. - c.-57044C>A r.(?) p.(=)
NPHP3 NM_153240.4 ?/. - c.785C>A r.(?) p.(Ser262Tyr)
NPHP3-ACAD11 NR_037804.1 ?/. - n.889C>A r.(?) -


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