Variant #0000016206 (NC_000009.11:g.35658025_35658026insGCTCAG, NR_003051.3:n.-6_-5insCCTGAG (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.35658025_35658026insGCTCAG
DNA change (hg38) g.35658028_35658029insGCTCAG
Published as insCCTGAG at -6
ISCN -
DB-ID RMRP_000033
Variant remarks 1 German CHH family (com-het)
Reference PubMed: Ridanpää et al. 2001, PubMed: Ridanpää et al. 2002
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency 0/280 CON
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 2012-11-08 12:48:41 +01:00 (CET)
Date last edited 2020-06-25 13:34:25 +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.-6_-5insCCTGAG r.0 -


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