Variant #0000016154 (NC_000009.11:g.35657945T>C, NR_003051.3:n.71A>G (RMRP))

Chromosome 9
Allele Unknown
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.35657945T>C
DNA change (hg38) g.35657948T>C
Published as 70A>G
ISCN -
DB-ID RMRP_000005 See all 4 reported entries
Variant remarks Finnish Major CHH mutation, (90> Finnish CHH families; most homozygous), and also the most common mutation (~48%) in other countries: Observed in American (also Amish), Australian, Austrian, Belgian, Brazilian, Canadian, Dutch, English, French, German, Turkish, Irish and Mexican CHH patients
Reference PubMed: Ridanpää et al. 2001&PubMed: 2002, PubMed: Bonafe et al. 2002&PubMed: 2005 and others PubMed: 2006, PubMed: 2008, PubMed: 2011, PubMed: 2012, PubMed: 2013
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency 10/845 FIN CON
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00088 View details
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2012-11-05 10:15:58 +01:00 (CET)
Date last edited 2020-06-25 13:28:20 +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.71A>G r.71a>g -


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