Variant #0000330840 (NC_000006.11:g.26204978C>T, NM_003545.3:c.106C>T (HIST1H4E))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.26204978C>T
DNA change (hg38) g.26204750C>T
Published as HIST1H4E(NM_003545.3):c.106C>T (p.(Arg36Trp))
ISCN -
DB-ID HIST1H4E_000001 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HIST1H2BF NM_003522.3 +/. - c.*4811C>T r.(=) p.(=)
HIST1H4E NM_003545.3 +/. - c.106C>T r.(?) p.(Arg36Trp)


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