Variant #0000508253 (NC_000001.10:g.66064470G>A, NM_002303.5:c.977G>A (LEPR))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.66064470G>A
DNA change (hg38) g.65598787G>A
Published as LEPR(NM_001003679.3):c.977G>A (p.R326H)
ISCN -
DB-ID LEPR_000032
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) 4.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +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.977G>A r.(?) p.(Arg326His)
LEPROT NM_017526.4 -?/. - c.*166868G>A r.(=) p.(=)


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