Variant #0000507406 (NC_000001.10:g.40562882A>T, NM_000310.3:c.29T>A (PPT1))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.40562882A>T
DNA change (hg38) g.40097210A>T
Published as PPT1(NM_000310.3):c.29T>A (p.L10*), PPT1(NM_000310.4):c.29T>A (p.(Leu10*))
ISCN -
DB-ID PPT1_000068 See all 14 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) 8.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPT1 NM_000310.3 +/. - c.29T>A r.(?) p.(Leu10Ter)


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