Variant #0000717662 (NC_000001.10:g.66074549C>A, NM_002303.5:c.1717C>A (LEPR))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.66074549C>A
DNA change (hg38) -
Published as LEPR(NM_001003679.3):c.1717C>A (p.R573S)
ISCN -
DB-ID LEPR_000053
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_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 N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LEPR NM_002303.5 ?/. - c.1717C>A r.(?) p.(Arg573Ser)
LEPROT NM_017526.4 ?/. - c.*176947C>A r.(=) p.(=)


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