Variant #0000929600 (NC_000009.11:g.35657916G>A, NR_003051.3:n.100C>T (RMRP))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.35657916G>A
DNA change (hg38) -
Published as RMRP(NR_003051.3):n.100C>T
ISCN -
DB-ID RMRP_000105
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) 9.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CA9 NM_001216.2 +?/. - c.-16041G>A r.(?) p.(=)
ARHGEF39 NM_032818.2 +?/. - c.*4068C>T r.(=) p.(=)
CCDC107 NM_174923.2 +?/. - c.-461G>A r.(?) p.(=)
RMRP NR_003051.3 +?/. - n.100C>T r.(?) -


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