Variant #0000016200 (NC_000009.11:g.35658006A>G, NR_003051.3:n.10T>C (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.35658006A>G
DNA change (hg38) g.35658009A>G
Published as 9T>C
ISCN -
DB-ID RMRP_000019
Variant remarks 1 German CHH patient (com-het)
Reference PubMed: Hermanns el al. 2006
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 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 13:42:00 +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.10T>C r.10u>c -


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