Variant #0000411540 (NC_000002.11:g.242695399G>A, NM_152783.3:c.1276G>A (D2HGDH))

Chromosome 2
Allele Parent #2
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.242695399G>A
DNA change (hg38) g.241755984G>A
Published as -
ISCN -
DB-ID D2HGDH_015020 See all 6 reported entries
Variant remarks -
Reference PubMed: Kranendijk 2010
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00719 View details
Owner Gajja Salomons
Database submission license No license selected
Created by Gajja Salomons
Date created 2016-01-05 10:44:38 +01:00 (CET)
Date last edited 2019-02-27 22:28:00 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
D2HGDH NM_152783.3 +/. 9 c.1276G>A r.(?) p.(Ala426Thr)



Screenings

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