Variant #0000925044 (NC_000009.11:g.35657962G>A, NR_003051.3:n.54C>T (RMRP))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.35657962G>A
DNA change (hg38) -
Published as RMRP(NR_003051.3):n.54C>T
ISCN -
DB-ID CA9_000019 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) 0.00287 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 2023-04-16 21:50:28 +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.-15995G>A r.(?) p.(=)
ARHGEF39 NM_032818.2 -?/. - c.*4022C>T r.(=) p.(=)
CCDC107 NM_174923.2 -?/. - c.-415G>A r.(?) p.(=)
RMRP NR_003051.3 -?/. - n.54C>T r.(?) -


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