Variant #0000717652 (NC_000001.10:g.66058513A>G, NM_002303.5:c.668A>G (LEPR))

Chromosome 1
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.66058513A>G
DNA change (hg38) -
Published as LEPR(NM_001003679.3):c.668A>G (p.Q223R), LEPR(NM_002303.5):c.668A>G (p.Q223R)
ISCN -
DB-ID LEPR_000030 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) 0.50547 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LEPR NM_002303.5 -/. - c.668A>G r.(?) p.(Gln223Arg)
LEPROT NM_017526.4 -/. - c.*160911A>G r.(=) p.(=)


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