Variant #0000016194 (NC_000009.11:g.35658027_35658028insCACAGAT, NR_003051.3:n.-13_-12insATCTGTG (RMRP))

Chromosome 9
Allele Maternal (confirmed)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.35658027_35658028insCACAGAT
DNA change (hg38) g.35658030_35658031insCACAGAT
Published as insertion ATCTGTG at -13
ISCN -
DB-ID RMRP_000013
Variant remarks 1 CHH patient with undetermined ethnicity (com-het)
Reference PubMed: Roifman et al. 2006
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 2012-11-07 13:05:36 +01:00 (CET)
Date last edited 2017-05-05 19:04:32 +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.-13_-12insATCTGTG r.0 -


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