Variant #0000349737 (NC_000017.10:g.37829490_37829492del, NM_002686.3:c.*2848_*2850del (PNMT))

Chromosome 17
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.37829490_37829492del
DNA change (hg38) g.39673237_39673239del
Published as -
ISCN -
DB-ID PGAP3_000009
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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PNMT NM_002686.3 ?/. - c.*2848_*2850del r.(=) p.(=)
PGAP3 NM_033419.3 ?/. - c.715_717del r.(?) p.(Trp239del)


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