Variant #0000997858 (NC_000009.11:g.35657840C>T, NR_003051.3:n.176G>A (RMRP))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.35657840C>T
DNA change (hg38) -
Published as RMRP(NR_003051.3):n.176G>A
ISCN -
DB-ID RMRP_000107
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) 0.00083 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 2024-08-28 13:16:32 +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.-16117C>T r.(?) p.(=)
ARHGEF39 NM_032818.2 ?/. - c.*4144G>A r.(=) p.(=)
CCDC107 NM_174923.2 ?/. - c.-537C>T r.(?) p.(=)
RMRP NR_003051.3 ?/. - n.176G>A r.(?) -


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