Variant #0001035648 (NC_000006.11:g.26204906G>T, NM_003545.3:c.34G>T (HIST1H4E))

Chromosome 6
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.26204906G>T
DNA change (hg38) -
Published as HIST1H4E(NM_003545.4):c.34G>T (p.(Gly12Cys))
ISCN -
DB-ID HIST1H2BF_000004
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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HIST1H2BF NM_003522.3 ?/. - c.*4739G>T r.(=) p.(=)
HIST1H4E NM_003545.3 ?/. - c.34G>T r.(?) p.(Gly12Cys)


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