Variant #0000000376 (NC_000011.10:g.5226963T>C, NM_000518.4:c.59A>G (HBB))

Individual ID 00000069
Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.5226963T>C
Published as CD 19 (AAC>AGC) / Hb Malay
Reference K G Yang et al. (1989), dbSNP, (OMIM 0168)ClinVar
DB-ID HBB_000012 See all 23 reported entries
dbSNP ID rs33972047
Frequency 6/41
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
Date created 2020-10-20 11:51:48 +08:00 (CST)
Date last edited 2021-08-19 10:39:46 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
HBB NM_000518.4 +/. 1 c.59A>G CD 19 (AAC>AGC) / Hb Malay r.(?) p.(Asn20Ser) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000082 DNA SEQ HBB 7 Nuur Athirah Binti Mohd Daud