Variant #0000288989 (NC_000023.10:g.71788730C>T, HDAC8(NM_018486.2):c.169G>A)

Chromosome X
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.71788730C>T
DNA change (hg38) g.72568880C>T
Published as HDAC8(NM_001166418.1):c.164+3177G>A (p.(=)), HDAC8(NM_001166419.1):c.169G>A (p.V57I)
ISCN -
DB-ID HDAC8_000022 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) 0.00023 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HDAC8 NM_018486.2 -/. - c.169G>A r.(?) p.(Val57Ile)