Variant #0001054443 (NC_000012.11:g.96389664G>A, NM_001258333.1:c.-533C>T (HAL))

Chromosome 12
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.96389664G>A
DNA change (hg38) -
Published as HAL(NM_002108.4):c.25C>T (p.(Arg9Cys))
ISCN -
DB-ID HAL_000027
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) 0.00026 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LTA4H NM_000895.2 -?/. - c.*5103C>T r.(=) p.(=)
HAL NM_001258333.1 -?/. - c.-533C>T r.(?) p.(=)


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