Variant #0000973971 (NC_000001.10:g.43688496C>T, NM_001159936.1:c.-50404G>A (EBNA1BP2))

Chromosome 1
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.43688496C>T
DNA change (hg38) -
Published as CFAP57(NM_001378189.1):c.2534C>T (p.(Ala845Val))
ISCN -
DB-ID EBNA1BP2_000002
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) 0.00054 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:20:39 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EBNA1BP2 NM_001159936.1 -?/. - c.-50404G>A r.(?) p.(=)
WDR65 NM_152498.3 -?/. - c.*12741C>T r.(=) p.(=)


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