Variant #0001035646 (NC_000006.11:g.26104443G>T, NM_003542.3:c.268G>T (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.26104443G>T
DNA change (hg38) -
Published as HIST1H4C(NM_003542.4):c.268G>T (p.(Ala90Ser))
ISCN -
DB-ID HIST1H1T_000011
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) 0.00033 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 2025-05-05 21:14:00 +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.268G>T r.(?) p.(Ala90Ser)
HIST1H1T NM_005323.3 -?/. - c.*3255C>A r.(=) p.(=)


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