Variant #0000528144 (NC_000006.11:g.26197415C>A, NM_003522.3:c.-2372C>A (HIST1H2BF))

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.26197415C>A
DNA change (hg38) g.26197187C>A
Published as HIST1H3D(NM_003530.4):c.64G>T (p.A22S)
ISCN -
DB-ID HIST1H2BF_000001
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HIST1H2BF NM_003522.3 ?/. - c.-2372C>A r.(?) p.(=)
HIST1H3D NM_003530.3 ?/. - c.64G>T r.(?) p.(Ala22Ser)
HIST1H2AD NM_021065.2 ?/. - c.*1664G>T r.(=) p.(=)


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