Variant #0000412579 (NC_000014.8:g.50769635T>C, L2HGDH(NM_024884.2):c.241A>G)

Individual ID 00185633
Chromosome 14
Allele Parent #2
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.50769635T>C
DNA change (hg38) g.50302917T>C
Published as -
ISCN -
DB-ID L2HGDH_000030 See all 27 reported entries
Variant remarks pathogenicity proven by overexpression studies
Reference PubMed: Rzem 2004, PubMed: Rzem 2006
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Gajja Salomons
Database submission license No license selected
Created by Gajja Salomons
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
L2HGDH NM_024884.2 +?/. 2 c.241A>G r.(?) p.(Lys81Glu)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000186599 DNA SEQ - - L2HGDH 2 Gajja Salomons