Variant #0000016192 (NC_000009.11:g.35658028_35658034dup, NR_003051.3:n.-19_-13dupTCTGTGA (RMRP))

Chromosome 9
Allele Unknown
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.35658028_35658034dup
DNA change (hg38) g.35658031_35658037dup
Published as dup TCTGTGA at -13; g.-20_-14dupTCTGTGA; -14_-20dupTCTGTGA; -20-14dup
ISCN -
DB-ID RMRP_000011
Variant remarks 2 American CHH families, 1 American CHH patient and 1 CHH family with undetermined ethnicity (all com-het)
Reference PubMed: Ridanpää et al. 2002, PubMed: Bonafe et al. 2005, PubMed: Hermanns el al. 2006, PubMed: Kavadas et al. 2008
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 2012-11-07 11:57:12 +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.-19_-13dupTCTGTGA r.? -


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