Variant #0000163053 (NC_000002.11:g.55910954G>A, NM_033109.4:c.419C>T (PNPT1))

Chromosome 2
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.55910954G>A
DNA change (hg38) g.55683819G>A
Published as g.55910954C>T
ISCN -
DB-ID PNPT1_000002
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner Sanna Matilainen
Database submission license No license selected
Created by Sanna Matilainen
Date created 2017-02-10 15:27:25 +01:00 (CET)
Date last edited 2017-02-19 11:22:36 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PNPT1 NM_033109.4 +?/. 5 c.419C>T r.(?) p.(Pro140Leu)



Screenings

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