Variant #0000016995 (NC_000009.11:g.35657924C>T, NR_003051.3:n.92G>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.35657924C>T
DNA change (hg38) g.35657927C>T
Published as 91G>A
ISCN -
DB-ID RMRP_000058
Variant remarks 1 Belgian CHH patient (com-het); Variants n.91G>A and n.101C>T are in same haplotype and it is unclear which of them is (or both are) causative
Reference PubMed: Hermanns el al. 2006
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 13:28:18 +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.92G>A r.92g>a -


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