Variant #0000443315 (NC_000017.10:g.40557182dup, NM_012232.5:c.696dup (PTRF))

Chromosome 17
Allele Parent #1
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.40557182dup
DNA change (hg38) g.42405164dup
Published as 696dupC
ISCN -
DB-ID PTRF_000001 See all 6 reported entries
Variant remarks expression cloned in C2C12/COS-7 cells gave microtubular filament network in cytoplasm, IP-no proper localization
Reference PubMed: Hayashi 2009
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2009-11-07 16:58:46 +01:00 (CET)
Date last edited 2012-11-02 20:43:03 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTRF NM_012232.5 +/. 2 c.696dup r.(?) p.(Lys233Glnfs*192)


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