Variant #0000538107 (NC_000009.11:g.35657947C>A, NR_003051.3:n.69G>T (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.35657947C>A
DNA change (hg38) g.35657950C>A
Published as RMRP(NR_003051.3):n.69G>T
ISCN -
DB-ID CA9_000008
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) Retrieve
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.-16010C>A r.(?) p.(=)
ARHGEF39 NM_032818.2 ?/. - c.*4037G>T r.(=) p.(=)
CCDC107 NM_174923.2 ?/. - c.-430C>A r.(?) p.(=)
RMRP NR_003051.3 ?/. - n.69G>T r.(?) -


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