Variant #0000971070 (NC_000023.10:g.39932808G>A, NM_001123385.1:c.1791C>T (BCOR))

Chromosome X
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.39932808G>A
DNA change (hg38) -
Published as BCOR(NM_001123383.1):c.1791C>T (p.(His597=), p.H597=), BCOR(NM_001123385.1):c.1791C>T (p.H597=), BCOR(NM_017745.6):c.1791C>T (p.H597=)
ISCN -
DB-ID BCOR_000107 See all 2 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) 0.03461 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 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BCOR NM_001123385.1 ?/. - c.1791C>T r.(?) p.(His597=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.