Variant #0000968253 (NC_000016.9:g.227377T>C, NM_000517.4:c.*3778T>C (HBA2))

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.227377T>C
DNA change (hg38) -
Published as HBA1(NM_000558.5):c.396T>C (p.S132=)
ISCN -
DB-ID HBA1_004008
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) 0.00024 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-02-26 20:06:56 +01:00 (CET)
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.*3778T>C - r.(=) p.(=)
HBA1 NM_000558.3 -?/. - c.396T>C - r.(?) p.(=)
HBQ1 NM_005331.4 -?/. - c.-3109T>C - r.(?) p.(=)


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