Variant #0000294612 (NC_000002.11:g.1748209C>A, NM_012293.1:c.19G>T (PXDN))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.1748209C>A
DNA change (hg38) g.1744437C>A
Published as PXDN(NM_012293.2):c.19G>T (p.G7C), PXDN(NM_012293.3):c.19G>T (p.G7C)
ISCN -
DB-ID PXDN_000027 See all 2 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) 0.00118 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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     
PXDN NM_012293.1 -?/. - c.19G>T r.(?) p.(Gly7Cys)


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