Variant #0000017000 (NC_000009.11:g.35657918_35657919dup, NR_003051.3:n.97_98dupTG (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.35657918_35657919dup
DNA change (hg38) g.35657921_35657922dupCA
Published as 98dupTG; dup TG at 98; g.96_97dupTG
ISCN -
DB-ID RMRP_000063
Variant remarks 2 Canadian and 2 Swiss CHH families (all com-het), 1 Turkish CHH family (hom)
Variant Error [EMISMATCH/0]: This transcript variant has an error. Please fix this entry and then remove this message.
Reference PubMed: Ridanpää et al. 2002, PubMed: Ridanpää et al. 2001, PubMed: Bonafe et al. 2005
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency 0/280 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 2013-01-30 15:07:13 +01:00 (CET)
Date last edited 2017-05-05 19:04:32 +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.97_98dupTG r.97_98dupug -


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