Genomic variant #0000274733

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.242681922C>T
DNA change (hg38) -
Published as D2HGDH(NM_152783.4):c.423C>T (p.P141=)
ISCN -
DB-ID D2HGDH_000002
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.00231 View details
Owner VKGL-NL




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
D2HGDH NM_152783.3 -?/. - c.423C>T likely benign r.(?) p.(=)