Variant #0000016186 (NC_000009.11:g.35657861C>A, NR_003051.3:n.155G>T (RMRP))

Chromosome 9
Allele Unknown
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.35657861C>A
DNA change (hg38) g.35657864C>A
Published as 154T
ISCN -
DB-ID RMRP_000006
Variant remarks 1 Finnish CHH family (com-het)
Reference PubMed: Ridanpää et al. 2002
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency 0/280 CON
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2012-11-05 11:15:24 +01:00 (CET)
Date last edited 2020-06-25 13:27:51 +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.155G>T r.155g>u -


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