Variant #0000282203 (NC_000001.10:g.66102257G>A, NM_002303.5:c.3057G>A (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.66102257G>A
DNA change (hg38) g.65636574G>A
Published as LEPR(NM_002303.5):c.3057G>A (p.P1019=), LEPR(NM_002303.6):c.3057G>A (p.P1019=)
ISCN -
DB-ID LEPR_000019 See all 3 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) 0.45675 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LEPR NM_002303.5 -/. - c.3057G>A r.(?) p.(Pro1019=)
LEPROT NM_017526.4 -/. - c.*204655G>A r.(=) p.(=)


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