Variant #0000557518 (NC_000016.9:g.230808C>T, NM_000558.3:c.*3398C>T (HBA1))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.230808C>T
DNA change (hg38) g.180809C>T
Published as HBQ1(NM_005331.4):c.239C>T (p.(Ala80Val))
ISCN -
DB-ID HBA1_003005
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) 0.00108 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
HBA1 NM_000558.3 -?/. - c.*3398C>T - r.(=) p.(=)
HBQ1 NM_005331.4 -?/. - c.239C>T - r.(?) p.(Ala80Val)


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