Variant #0000248823 (NC_000014.8:g.50778816A>C, L2HGDH(NM_024884.2):c.53T>G)

Chromosome 14
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.50778816A>C
DNA change (hg38) g.50312098A>C
Published as L2HGDH(NM_024884.3):c.53T>G (p.L18R)
ISCN -
DB-ID L2HGDH_000079 See all 2 reported entries
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) 0.56603 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP5S NM_015684.3 -/. - c.-923A>C r.(?) p.(=)
L2HGDH NM_024884.2 -/. - c.53T>G r.(?) p.(Leu18Arg)