Variant #0000800538 (NC_000002.11:g.25384618A>G, NM_000939.2:c.136T>C (POMC))

Chromosome 2
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.25384618A>G
DNA change (hg38) -
Published as POMC(NM_001319204.1):c.136T>C (p.C46R)
ISCN -
DB-ID EFR3B_000016
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POMC NM_000939.2 ?/. - c.136T>C r.(?) p.(Cys46Arg)
EFR3B NM_014971.1 ?/. - c.*7409A>G r.(=) p.(=)


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