Variant #0001063085 (NC_000001.10:g.66081863C>T, NM_002303.5:c.2168C>T (LEPR))

Chromosome 1
Allele Unknown
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.66081863C>T
DNA change (hg38) -
Published as LEPR(NM_002303.5):c.2168C>T (p.S723F), LEPR(NM_002303.6):c.2168C>T (p.(Ser723Phe))
ISCN -
DB-ID LEPR_000012 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LEPR NM_002303.5 +/. - c.2168C>T r.(?) p.(Ser723Phe)
LEPROT NM_017526.4 +/. - c.*184261C>T r.(=) p.(=)


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