Variant #0000619545 (NC_000023.10:g.39933973G>A, NM_001123385.1:c.626C>T (BCOR))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.39933973G>A
DNA change (hg38) g.40074720G>A
Published as BCOR(NM_001123383.1):c.626C>T (p.(Ser209Leu)), BCOR(NM_001123385.1):c.626C>T (p.S209L), BCOR(NM_017745.6):c.626C>T (p.S209L)
ISCN -
DB-ID BCOR_000058 See all 4 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) 0.00057 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
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     
BCOR NM_001123385.1 -/. - c.626C>T r.(?) p.(Ser209Leu)


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