Variant #0001070276 (NC_000001.10:g.26795615C>G, NM_205861.2:c.995C>G (DHDDS))

Chromosome 1
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.26795615C>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID DHDDS_000021 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs770732789
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-03-10 12:26:02 +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     
DHDDS NM_205861.2 ?/. - c.995C>G r.(?) p.(Ser332Ter)


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