Variant #0000992757 (NC_000002.11:g.25384076G>T, NM_000939.2:c.678C>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.25384076G>T
DNA change (hg38) -
Published as POMC(NM_001035256.1):c.678C>A (p.(Phe226Leu))
ISCN -
DB-ID EFR3B_000020
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 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 2024-08-28 13:07:21 +02:00 (CEST)
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.678C>A r.(?) p.(Phe226Leu)
EFR3B NM_014971.1 ?/. - c.*6867G>T r.(=) p.(=)


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