Variant #0000017007 (NC_000009.11:g.35657869C>T, NR_003051.3:n.147G>A (RMRP))

Chromosome 9
Allele Parent #1
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.35657869C>T
DNA change (hg38) g.35657872C>T
Published as 146A; g.146G>A
ISCN -
DB-ID RMRP_000070 See all 2 reported entries
Variant remarks 1 Chinese CHH family (hom), 1 French CHH family (com-het) and 2 CHH families (com-het) with undetermined ethnicity
Reference PubMed: Ridanpää et al. 2002, PubMed: Bonafe et al. 2005, 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) 5.0E-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 2013-01-30 15:07:13 +01:00 (CET)
Date last edited 2020-06-25 13:27:52 +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.147G>A r.147g>a -


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