Variant #0000610252 (NC_000006.11:g.26157054dup, NM_005321.2:c.436dup (HIST1H1E))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.26157054dup
DNA change (hg38) g.26156826dup
Published as -
ISCN -
DB-ID HIST1H1E_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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-18 15:07:59 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HIST1H1E NM_005321.2 +?/. - c.436dup r.(?) p.(Thr146AsnfsTer50)
HIST1H2BD NM_021063.3 +?/. - c.-1344dup r.(?) p.(=)


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