Variant #0000017006 (NC_000009.11:g.35657888C>G, NR_003051.3:n.128G>C (RMRP))

Chromosome 9
Allele Parent #1
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.35657888C>G
DNA change (hg38) g.35657891C>G
Published as 127G>C
ISCN -
DB-ID RMRP_000069 See all 2 reported entries
Variant remarks 1 American CHH patient (het)
Reference PubMed: Hermanns el al. 2006
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency 0/200 CON
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00254 View details
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 13:27:53 +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.128G>C r.128g>c -


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