Variant #0000995617 (NC_000006.11:g.27107397T>G, NM_003495.2:c.310T>G (HIST1H4I))

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.27107397T>G
DNA change (hg38) -
Published as HIST1H4I(NM_003495.2):c.310T>G (p.(Ter104Gluext*?))
ISCN -
DB-ID HIST1H2BK_000003
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HIST1H4I NM_003495.2 ?/. - c.310T>G r.(?) p.(*104Gluext*4)
HIST1H2BK NM_080593.2 ?/. - c.*10-937A>C r.(=) p.(=)


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