Variant #0000528149 (NC_000006.11:g.27835133C>T, NM_005322.2:c.175G>A (HIST1H1B))

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.27835133C>T
DNA change (hg38) g.27867355C>T
Published as H1-5(NM_005322.3):c.175G>A (p.G59S)
ISCN -
DB-ID HIST1H1B_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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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     
HIST1H2AL NM_003511.2 ?/. - c.*1608C>T r.(=) p.(=)
HIST1H3I NM_003533.2 ?/. - c.*4550G>A r.(=) p.(=)
HIST1H1B NM_005322.2 ?/. - c.175G>A r.(?) p.(Gly59Ser)


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