Variant #0000302958 (NC_000023.10:g.47003927G>T, NM_005676.4:c.-1083G>T (RBM10))

Chromosome X
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.47003927G>T
DNA change (hg38) g.47144528G>T
Published as NDUFB11(NM_001135998.2):c.152C>A (p.(Pro51Gln)), NDUFB11(NM_019056.6):c.152C>A (p.P51Q)
ISCN -
DB-ID NDUFB11_000007 See all 2 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) 0.00041 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RBM10 NM_005676.4 -?/. - c.-1083G>T r.(?) p.(=)
NDUFB11 NM_019056.6 -?/. - c.152C>A r.(?) p.(Pro51Gln)


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