Variant #0000607843 (NC_000002.11:g.240056228A>T, NM_006037.3:c.1090T>A (HDAC4))

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.240056228A>T
DNA change (hg38) g.239134532A>T
Published as HDAC4(NM_001378414.1):c.1090T>A (p.(Ser364Thr)), HDAC4(NM_006037.3):c.1090T>A (p.S364T)
ISCN -
DB-ID HDAC4_000049 See all 2 reported entries
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2026-01-20 18:57:21 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HDAC4 NM_006037.3 -?/. - c.1090T>A r.(?) p.(Ser364Thr)


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