Variant #0000274989 (NC_000001.10:g.26795513G>A, NM_024887.3:c.896G>A (DHDDS))

Chromosome 1
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.26795513G>A
DNA change (hg38) g.26469022G>A
Published as DHDDS(NM_024887.3):c.896G>A (p.R299H)
ISCN -
DB-ID DHDDS_000003
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) 5.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HMGN2 NM_005517.3 -?/. - c.-3591G>A r.(?) p.(=)
DHDDS NM_024887.3 -?/. - c.896G>A r.(?) p.(Arg299His)
DHDDS NM_205861.2 -?/. - c.893G>A r.(?) p.(Arg298His)


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