Variant #0000995621 (NC_000006.11:g.27860872G>A, NM_003514.2:c.56C>T (HIST1H2AM))

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.27860872G>A
DNA change (hg38) -
Published as HIST1H2AM(NM_003514.2):c.56C>T (p.(Ser19Phe))
ISCN -
DB-ID HIST1H2AM_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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HIST1H2AM NM_003514.2 ?/. - c.56C>T r.(?) p.(Ser19Phe)
HIST1H2BO NM_003527.4 ?/. - c.-369G>A r.(?) p.(=)
HIST1H3J NM_003535.2 ?/. - c.-2302C>T r.(?) p.(=)
OR2B6 NM_012367.1 ?/. - c.-64147G>A r.(?) p.(=)
OR2B2 NM_033057.2 ?/. - c.*18152C>T r.(=) p.(=)


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