Variant #0000974086 (NC_000001.10:g.66036336C>T, NM_002303.5:c.221C>T (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.66036336C>T
DNA change (hg38) -
Published as LEPR(NM_002303.6):c.221C>T (p.S74L)
ISCN -
DB-ID LEPR_000088
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-04-19 20:20:39 +02:00 (CEST)
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.221C>T r.(?) p.(Ser74Leu)
LEPROT NM_017526.4 ?/. - c.*138734C>T r.(=) p.(=)


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