Variant #0000659029 (NC_000023.10:g.103294668G>A, NM_001164416.1:c.125G>A (H2BFM))

Chromosome X
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.103294668G>A
DNA change (hg38) g.104040101G>A
Published as H2BFM(NM_001164416.1):c.125G>A (p.(Arg42Gln))
ISCN -
DB-ID H2BFM_000008
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) 0.00308 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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
H2BFM NM_001164416.1 -?/. - c.125G>A r.(?) p.(Arg42Gln)


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