Variant #0000981777 (NC_000016.9:g.227011G>A, NM_000517.4:c.*3412G>A (HBA2))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.227011G>A
DNA change (hg38) -
Published as HBA1(NM_000558.5):c.179G>A (p.(Gly60Asp))
ISCN -
DB-ID HBA1_000077 See all 2 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) Retrieve
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.*3412G>A - r.(=) p.(=)
HBA1 NM_000558.3 +?/. - c.179G>A - r.(?) p.(Gly60Asp)
HBQ1 NM_005331.4 +?/. - c.-3475G>A - r.(?) p.(=)


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