Variant #0000538108 (NC_000009.11:g.35657952G>A, NR_003051.3:n.64C>T (RMRP))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.35657952G>A
DNA change (hg38) g.35657955G>A
Published as RMRP(NR_003051.3):n.64C>T
ISCN -
DB-ID RMRP_000050 See all 3 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CA9 NM_001216.2 +/. - c.-16005G>A r.(?) p.(=)
ARHGEF39 NM_032818.2 +/. - c.*4032C>T r.(=) p.(=)
CCDC107 NM_174923.2 +/. - c.-425G>A r.(?) p.(=)
RMRP NR_003051.3 +/. - n.64C>T r.(?) -


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