Variant #0000320720 (NC_000001.10:g.32797336C>T, NM_004964.2:c.1148C>T (HDAC1))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.32797336C>T
DNA change (hg38) g.32331735C>T
Published as HDAC1(NM_004964.2):c.1148C>T (p.(Ala383Val))
ISCN -
DB-ID HDAC1_000002
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) 0.00011 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HDAC1 NM_004964.2 ?/. - c.1148C>T r.(?) p.(Ala383Val)
MARCKSL1 NM_023009.6 ?/. - c.*2862G>A r.(=) p.(=)


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