Variant #0000576087 (NC_000023.10:g.47004861T>C, NM_005676.4:c.-149T>C (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.47004861T>C
DNA change (hg38) g.47145462T>C
Published as RBM10(NM_001204466.1):c.-149T>C (p.(=))
ISCN -
DB-ID RBM10_000028
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) 0.01834 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RBM10 NM_005676.4 -?/. - c.-149T>C r.(?) p.(=)
NDUFB11 NM_019056.6 -?/. - c.-783A>G r.(?) p.(=)


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