Variant #0001027493 (NC_000023.10:g.39932564C>T, NM_001123385.1:c.2035G>A (BCOR))

Chromosome X
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.39932564C>T
DNA change (hg38) -
Published as BCOR(NM_001123385.1):c.2035G>A (p.V679I), BCOR(NM_001123385.2):c.2035G>A (p.(Val679Ile)), BCOR(NM_017745.6):c.2035G>A (p.V679I)
ISCN -
DB-ID BCOR_000051 See all 5 reported entries
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BCOR NM_001123385.1 -?/. - c.2035G>A r.(?) p.(Val679Ile)


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