Variant #0001050541 (NC_000002.11:g.25384171C>T, NM_000939.2:c.583G>A (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.25384171C>T
DNA change (hg38) -
Published as POMC(NM_000939.4):c.583G>A (p.(Ala195Thr)), POMC(NM_001035256.2):c.583G>A (p.A195T), POMC(NM_001035256.3):c.583G>A (p.A195T)
ISCN -
DB-ID EFR3B_000013 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) 0.0005 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POMC NM_000939.2 ?/. - c.583G>A r.(?) p.(Ala195Thr)
EFR3B NM_014971.1 ?/. - c.*6962C>T r.(=) p.(=)


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