Variant #0000016191 (NC_000009.11:g.35658025_35658039[3], NR_003051.3:n.-24_-10ACTACTCTGTGAAGC[3] (RMRP))

Chromosome 9
Allele Paternal (confirmed)
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.35658025_35658039[3]
DNA change (hg38) -
Published as Two times dupACTACTCTGTGAAGC at -10
ISCN -
DB-ID RMRP_000030
Variant remarks 1 Swiss CHH family (com-het)
Reference PubMed: Ridanpää et al. 2001, PubMed: Ridanpää et al. 2002
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
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 11:22:37 +01:00 (CET)
Date last edited 2017-05-05 18:33:04 +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.-24_-10ACTACTCTGTGAAGC[3] r.0 -


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