Variant #0000016989 (NC_000009.11:g.35657946_35657947delinsAA, NR_003051.3:n.69_70delinsTT (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.35657946_35657947delinsAA
DNA change (hg38) g.35657949_35657950delinsAA
Published as g.68_69delinsTT
ISCN -
DB-ID RMRP_000052
Variant remarks 1 CHH patient (com-het) with undetermined ethnicity
Reference PubMed: Horn et al. 2010
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 2013-01-30 15:07:13 +01:00 (CET)
Date last edited 2020-06-25 13:28:21 +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.69_70delinsTT r.69_70delinsuu -


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