Variant #0000000231 (NC_000019.9:g.12995713T>G, KLF1(NM_006563.3):c.1075A>C)

Individual ID 00002103
Chromosome 19
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.12995713T>G
Reference Shang X,et al
DB-ID KLF1_000015
Frequency 1/20222
Variant remarks Elevated HbF
ClassClinical Likely pathogenic
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KLF1 NM_006563.3 ./. 3 c.1075A>C r.(?) p.(Lys359Gln)



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002105 DNA SEQ-NG-I KLF1 1 Qi Ming