Variant #0000515438 (NC_000002.11:g.25384596T>C, NM_000939.2:c.158A>G (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.25384596T>C
DNA change (hg38) g.25161727T>C
Published as POMC(NM_001035256.2):c.158A>G (p.D53G), POMC(NM_001035256.3):c.158A>G (p.D53G)
ISCN -
DB-ID POMC_000012 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) 0.00089 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POMC NM_000939.2 ?/. - c.158A>G r.(?) p.(Asp53Gly)
EFR3B NM_014971.1 ?/. - c.*7387T>C r.(=) p.(=)


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