Full data view for gene CLPP

Information The variants shown are described using the NM_006012.2 transcript reference sequence.

4 entries on 1 page. Showing entries 1 - 4.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. 2i c.270+1G>A r.[270_271insains270+2_271-1, =, ?] p.[Ile91Valfs*39, =, ?] Unknown - NA g.6361955A>G g.6361944A>G - - CLPP_000009 in vitro COS7 cell expression cloning; 23/37 clones normal splicing, 11/37 retained intron 2, 3/37 other aberrant transcripts Variant Error [EMISMATCH]: This variant seems to mismatch; the genomic and the transcript variant seems to not belong together. Please fix this entry and then remove this message. PubMed: Jenkinson 2013, Journal: Jenkinson 2013 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
+/. 2i c.270+4A>G r.spl? p.? Unknown - pathogenic g.6361955A>G g.6361944A>G - - CLPP_000009 not in 772 control chromosomes PubMed: Jenkinson 2013, Journal: Jenkinson 2013, OMIM:var0003 - rs398123035 Germline yes - - - - DNA SEQ - - PRLTS - PubMed: Jenkinson 2013, Journal: Jenkinson 2013 4-generation family, 3 affecteds (2F, M), unaffected heterozygous carrier parents F;M yes Pakistan - - - - - 3 Johan den Dunnen
+/. 2i c.270+4A>G r.[270_271insgtggins270+5_271-1, 255_270del]] p.[Ile91Valfs*39, Cys246Serfs*36] Unknown - NA g.6361955A>G g.6361944A>G - - CLPP_000009 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 PubMed: Jenkinson 2013, Journal: Jenkinson 2013 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
+/+ 2i c.270+4A>G r.spl? p.? Parent #1 - pathogenic g.6361955A>G g.6361944A>G - - CLPP_000009 - MORL Deafness Variation Database, PubMed: Jenkinson 2013, PubMed: Szafranski 2015 - - SUMMARY record - - - - - DNA ? - - PRLTS - PubMed: Jenkinson 2013, PubMed: Szafranski 2015 - - - - - - - - - 1 Global Variome, with Curator vacancy
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