Variant #0000975176 (NC_000002.11:g.26461966T>G, NC_000002.11(NM_000182.4):c.109+4A>C (HADHA))

Chromosome 2
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.26461966T>G
DNA change (hg38) -
Published as HADHA(NM_000182.5):c.109+4A>C
ISCN -
DB-ID HADHA_000037
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 20:20:39 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HADHA NM_000182.4 -?/. - c.109+4A>C r.spl? p.?
HADHB NM_000183.2 -?/. - c.-5901T>G r.(?) p.(=)


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