Variant #0000800990 (NC_000003.11:g.132394142T>C, NM_153240.4:c.*6612A>G (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.132394142T>C
DNA change (hg38) -
Published as UBA5(NM_024818.4):c.863T>C (p.M288T)
ISCN -
DB-ID ACAD11_000052
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) 2.0E-5 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +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.863T>C r.(?) p.(Met288Thr)
ACAD11 NM_032169.4 ?/. - c.-15547A>G r.(?) p.(=)
NPHP3 NM_153240.4 ?/. - c.*6612A>G r.(=) p.(=)
NPHP3-ACAD11 NR_037804.1 ?/. - n.3995+6616A>G r.(?) -


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