Variant #0000252382 (NC_000002.11:g.25384324A>G, NM_000939.2:c.430T>C (POMC))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.25384324A>G
DNA change (hg38) g.25161455A>G
Published as POMC(NM_001035256.2):c.430T>C (p.F144L), POMC(NM_001035256.3):c.430T>C (p.F144L)
ISCN -
DB-ID POMC_000004 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) 0.00018 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.430T>C r.(?) p.(Phe144Leu)
EFR3B NM_014971.1 +?/. - c.*7115A>G r.(=) p.(=)


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