Variant #0000528137 (NC_000006.11:g.26156725C>G, NM_005321.2:c.107C>G (HIST1H1E))

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.26156725C>G
DNA change (hg38) g.26156497C>G
Published as HIST1H1E(NM_005321.3):c.107C>G (p.(Ser36Cys))
ISCN -
DB-ID HIST1H1E_000002
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +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.107C>G r.(?) p.(Ser36Cys)
HIST1H2BD NM_021063.3 ?/. - c.-1673C>G r.(?) p.(=)


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