Variant #0000016199 (NC_000009.11:g.35658011G>A, NR_003051.3:n.5C>T (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.35658011G>A
DNA change (hg38) g.35658014G>A
Published as 4T; g.4C>T; 4C>T
ISCN -
DB-ID RMRP_000018
Variant remarks 1 Australian, 1 Dutch, 1 English, 1 German, 1 Spanish, 1 Swiss and 1 Italian CHH family, 1 German CHH patient and 2 CHH patients and 1 CHH family with undetermined ethnicity (all com-het)
Reference PubMed: Ridanpää et al. 2002, PubMed: Bonafe 2005, PubMed: Roifman 2006, PubMed: Hermanns 2006, PubMed: Munoz-Robles 2006 and PubMed: Kavadas 2008, PubMed: Bacchetta 2009
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency 0/280 CON
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00011 View details
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 13:32:46 +01:00 (CET)
Date last edited 2020-06-25 13:30:02 +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.5C>T r.5c>u -


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