Variant #0000524604 (NC_000005.9:g.141014382C>T, NM_003883.3:c.277G>A (HDAC3))

Chromosome 5
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.141014382C>T
DNA change (hg38) g.141634815C>T
Published as HDAC3(NM_003883.3):c.277G>A (p.(Asp93Asn))
ISCN -
DB-ID HDAC3_000002 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-10 15:20:10 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HDAC3 NM_003883.3 ?/. - c.277G>A r.(?) p.(Asp93Asn)
FCHSD1 NM_033449.2 ?/. - c.*6683G>A r.(=) p.(=)
RELL2 NM_173828.4 ?/. - c.-3411C>T r.(?) p.(=)


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