Variant #0000266813 (NC_000014.8:g.24775579C>T, XM_005267385.1:c.*1278C>T (NOP9))

Chromosome 14
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.24775579C>T
DNA change (hg38) g.24306373C>T
Published as CIDEB(NM_014430.4):c.336+1G>A
ISCN -
DB-ID CIDEB_000001
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) 0.00068 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
LTB4R NM_001143919.2 ?/. - c.-5447C>T r.(?) p.(=)
LTB4R2 NM_001164692.2 ?/. - c.-3949C>T r.(?) p.(=)
CIDEB NM_014430.2 ?/. - c.336+1G>A r.spl? p.?
NOP9 XM_005267385.1 ?/. - c.*1278C>T r.(=) p.(=)


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