Variant #0000139991 (NC_000019.9:g.6361955A>G, NC_000019.9(NM_006012.2):c.270+4A>G (CLPP))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.6361955A>G
DNA change (hg38) g.6361944A>G
Published as -
ISCN -
DB-ID CLPP_000009 See all 4 reported entries
Variant remarks in vitro COS7 cell expression cloning; 41/49 clones retained intron 2, 2/49 used cryptic donor
site (c.255), 5/49 aberrant splicing (excl. either exon 2 or exon 3, most likely artifacts), 1/49 normal splicing
Reference PubMed: Jenkinson 2013, Journal: Jenkinson 2013
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
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 2016-11-10 11:01:43 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLPP NM_006012.2 +/. 2i c.270+4A>G r.[270_271insgtggins270+5_271-1, 255_270del]] p.[Ile91Valfs*39, Cys246Serfs*36]


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