Variant #0000621685 (NC_000006.11:g.27114317G>A, NM_003495.2:c.*6918G>A (HIST1H4I))

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.27114317G>A
DNA change (hg38) g.27146538G>A
Published as HIST1H2BK(NM_080593.2):c.261C>T (p.R87=)
ISCN -
DB-ID HIST1H2BK_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 2019-12-06 12:43:26 +01:00 (CET)
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     
HIST1H4I NM_003495.2 -?/. - c.*6918G>A r.(=) p.(=)
HIST1H2BK NM_080593.2 -?/. - c.261C>T r.(?) p.(Arg87=)
HIST1H2AH NM_080596.1 -?/. - c.-591G>A r.(?) p.(=)


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