Variant #0000016221 (NC_000009.11:g.35658017_35658032dup, NR_003051.3:n.-15_1dupTGAAGCTGAGGACGTG (RMRP))

Chromosome 9
Allele Paternal (confirmed)
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.35658017_35658032dup
DNA change (hg38) g.35658020_35658035dup
Published as 16-bp dup at +1
ISCN -
DB-ID RMRP_000035
Variant remarks 1 Japanese CHH family (com-het)
Reference PubMed: Hirose et al. 2006
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency 0/65 JAP CON
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 2012-11-12 13:51:57 +01:00 (CET)
Date last edited 2020-06-25 13:31:08 +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.-15_1dupTGAAGCTGAGGACGTG r.? -


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