Variant #0000506939 (NC_000001.10:g.26764735G>A, NM_024887.3:c.140G>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.26764735G>A
DNA change (hg38) g.26438244G>A
Published as DHDDS(NM_024887.4):c.140G>A (p.R47Q)
ISCN -
DB-ID DHDDS_000014
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) 0.00073 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
DHDDS NM_024887.3 -?/. - c.140G>A r.(?) p.(Arg47Gln)
DHDDS NM_205861.2 -?/. - c.140G>A r.(?) p.(Arg47Gln)


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