Variant #0000911669 (NC_000002.11:g.26417950C>G, NC_000002.11(NM_000182.4):c.1620+11G>C (HADHA))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.26417950C>G
DNA change (hg38) -
Published as HADHA(NM_000182.5):c.1620+11G>C
ISCN -
DB-ID HADHA_000035
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) 0.00463 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +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     
HADHA NM_000182.4 -/. - c.1620+11G>C r.(=) p.(=)
HADHB NM_000183.2 -/. - c.-49917C>G r.(?) p.(=)


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