Variant #0000717667 (NC_000001.10:g.66096104_66096105dup, NC_000001.10(NM_002303.5):c.2674-5770_2674-5769dup (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.66096104_66096105dup
DNA change (hg38) -
Published as LEPR(NM_001198687.2):c.*16_*17dupAA
ISCN -
DB-ID LEPR_000057
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 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LEPR NM_002303.5 -/. - c.2674-5770_2674-5769dup r.(=) p.(=)
LEPROT NM_017526.4 -/. - c.*198502_*198503dup r.(=) p.(=)


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