Variant #0000981776 (NC_000016.9:g.226986G>A, NM_000517.4:c.*3387G>A (HBA2))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.226986G>A
DNA change (hg38) -
Published as HBA1(NM_000558.5):c.154G>A (p.(Gly52Ser), p.G52S)
ISCN -
DB-ID HBA1_000230 See all 3 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) 0.0003 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
HBA2 NM_000517.4 ?/. - c.*3387G>A - r.(=) p.(=)
HBA1 NM_000558.3 ?/. - c.154G>A - r.(?) p.(Gly52Ser)
HBQ1 NM_005331.4 ?/. - c.-3500G>A - r.(?) p.(=)


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