Variant #0000000206 (NC_000002.11:g.60719970C>A, BCL11A(NM_022893.3):c.386-24002G>T)

Chromosome 2
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) g.60719970C>A
Reference dbSNP
DB-ID BCL11A_000013 See all 2 reported entries
Frequency 35/60
Variant remarks Correlation Between Fetal Hemoglobin and Single Nucleotide Polymorphism at BCL11A Gene in major beta-thalassemia Patients in Guangxi province.
ClassClinical Likely benign
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BCL11A NM_022893.3 ./. - c.386-24002G>T r.(=) p.(=)