Variant #0000842133 (NC_000002.11:g.60688975dup, NM_022893.3:c.1078dup (BCL11A))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.60688975dup
DNA change (hg38) -
Published as -
ISCN -
DB-ID BCL11A_000051 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs768799046
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-03-07 12:09:01 +01:00 (CET)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BCL11A NM_022893.3 +/. - c.1078dup r.(?) p.(Leu360ProfsTer212)


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