Variant #0000966790 (NC_000012.11:g.124887090_124887095dup, NM_006312.5:c.1526_1531dup (NCOR2))

Chromosome 12
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.124887090_124887095dup
DNA change (hg38) -
Published as NCOR2(NM_001206654.2):c.1523_1528dupAGCAGC (p.Q508_Q509dup)
ISCN -
DB-ID NCOR2_000043 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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NCOR2 NM_006312.5 -/. - c.1526_1531dup r.(?) p.(Gln509_Gln510dup)


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