Variant #0000887135 (NC_000006.11:g.26156950C>T, NM_005321.2:c.332C>T (HIST1H1E))

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.26156950C>T
DNA change (hg38) -
Published as H1-4(NM_005321.3):c.332C>T (p.A111V)
ISCN -
DB-ID HIST1H1E_000016
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) 8.0E-5 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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HIST1H1E NM_005321.2 -?/. - c.332C>T r.(?) p.(Ala111Val)
HIST1H2BD NM_021063.3 -?/. - c.-1448C>T r.(?) p.(=)


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