Variant #0000995605 (NC_000006.11:g.26108299G>A, NM_003542.3:c.*3812G>A (HIST1H4C))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.26108299G>A
DNA change (hg38) -
Published as HIST1H1T(NM_005323.3):c.23C>T (p.(Ala8Val))
ISCN -
DB-ID HIST1H1T_000009
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) 0.00017 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HIST1H4C NM_003542.3 -?/. - c.*3812G>A r.(=) p.(=)
HIST1H1T NM_005323.3 -?/. - c.23C>T r.(?) p.(Ala8Val)


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