Variant #0001057320 (NC_000023.10:g.47003879T>C, NM_005676.4:c.-1131T>C (RBM10))

Chromosome X
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.47003879T>C
DNA change (hg38) -
Published as NDUFB11(NM_001135998.3):c.200A>G (p.(Tyr67Cys))
ISCN -
DB-ID RBM10_000056
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RBM10 NM_005676.4 ?/. - c.-1131T>C r.(?) p.(=)
NDUFB11 NM_019056.6 ?/. - c.200A>G r.(?) p.(Tyr67Cys)


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