Variant #0000653994 (NC_000001.10:g.26795615C>G, NM_024887.3:c.998C>G (DHDDS))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.26795615C>G
DNA change (hg38) g.26469124C>G
Published as DHDDS(NM_001319959.1):c.716C>G (p.S239*)
ISCN -
DB-ID DHDDS_000021
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) 1.0E-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 2020-03-23 16:13:27 +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.-3489C>G r.(?) p.(=)
DHDDS NM_024887.3 +/. - c.998C>G r.(?) p.(Ser333Ter)
DHDDS NM_205861.2 +/. - c.995C>G r.(?) p.(Ser332Ter)


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