Variant #0000993733 (NC_000003.11:g.47453880G>A, NM_015466.2:c.4286G>A (PTPN23))

Chromosome 3
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.47453880G>A
DNA change (hg38) -
Published as PTPN23(NM_015466.2):c.4286G>A (p.(Arg1429Gln))
ISCN -
DB-ID PTPN23_000027
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
SCAP NM_012235.2 +?/. - c.*1464C>T r.(=) p.(=)
PTPN23 NM_015466.2 +?/. - c.4286G>A r.(?) p.(Arg1429Gln)


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