Variant #0000982453 (NC_000017.10:g.37829376G>A, NM_002686.3:c.*2734G>A (PNMT))

Chromosome 17
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.37829376G>A
DNA change (hg38) -
Published as PGAP3(NM_033419.5):c.827C>T (p.(Pro276Leu), p.P276L)
ISCN -
DB-ID PGAP3_000006 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) 6.0E-5 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PNMT NM_002686.3 +?/. - c.*2734G>A r.(=) p.(=)
PGAP3 NM_033419.3 +?/. - c.827C>T r.(?) p.(Pro276Leu)


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