Variant #0000334013 (NC_000023.10:g.48681883C>T, NM_006044.2:c.3074C>T (HDAC6))

Chromosome X
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.48681883C>T
DNA change (hg38) g.48823473C>T
Published as HDAC6(NM_001321226.1):c.3074C>T (p.S1025L), HDAC6(NM_006044.2):c.3074C>T (p.(Ser1025Leu)), HDAC6(NM_006044.3):c.3074C>T (p.S1025L)
ISCN -
DB-ID HDAC6_000026 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) 0.00186 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 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HDAC6 NM_006044.2 ?/. - c.3074C>T r.(?) p.(Ser1025Leu)


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