Variant #0000039758 (NC_000009.11:g.35658039_35658040insGAGGAGTAGT, NR_003051.3:n.-18_-17insCTCACTACTC (RMRP))

Chromosome 9
Allele Maternal (confirmed)
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.35658039_35658040insGAGGAGTAGT
DNA change (hg38) g.35658042_35658043insGAGGAGTAGT
Published as M29916.1: g.726_727insCTCACTACTC
ISCN -
DB-ID RMRP_000103
Variant remarks 1 patient with CHH (com-het); 10-nucleotide insertion at position -18 in the promoter region of the RMRP gene
Reference PubMed: Crahes et al. 2013
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2014-07-26 19:52:33 +02:00 (CEST)
Date last edited 2020-06-25 13:39:12 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RMRP NR_003051.3 +?/+? - n.-18_-17insCTCACTACTC r.? -


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