Variant #0001025199 (NC_000006.11:g.26104188G>A, NM_003542.3:c.13G>A (HIST1H4C))

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.26104188G>A
DNA change (hg38) -
Published as H4C3(NM_003542.4):c.13G>A (p.G5S)
ISCN -
DB-ID HIST1H1T_000010
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 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HIST1H4C NM_003542.3 ?/. - c.13G>A r.(?) p.(Gly5Ser)
HIST1H1T NM_005323.3 ?/. - c.*3510C>T r.(=) p.(=)


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