Variant #0000528136 (NC_000006.11:g.26124738A>C, NM_003512.3:c.278A>C (HIST1H2AC))

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.26124738A>C
DNA change (hg38) g.26124510A>C
Published as HIST1H2AC(NM_003512.3):c.278A>C (p.(Glu93Ala))
ISCN -
DB-ID HIST1H2AC_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_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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HIST1H2AC NM_003512.3 ?/. - c.278A>C r.(?) p.(Glu93Ala)
HIST1H2BC NM_003526.2 ?/. - c.-606T>G r.(?) p.(=)


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