Variant #0000799503 (NC_000001.10:g.66095962A>C, NC_000001.10(NM_002303.5):c.2674-5912A>C (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.66095962A>C
DNA change (hg38) -
Published as LEPR(NM_001003680.3):c.2751A>C (p.G917=), LEPR(NM_001198687.2):c.2751A>C (p.G917=)
ISCN -
DB-ID LEPR_000072 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) 0.00638 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LEPR NM_002303.5 -/. - c.2674-5912A>C r.(=) p.(=)
LEPROT NM_017526.4 -/. - c.*198360A>C r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.