Variant #0000810412 (NC_000023.10:g.47041362T>C, NM_005676.4:c.1706T>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.47041362T>C
DNA change (hg38) -
Published as RBM10(NM_001204468.1):c.1901T>C (p.V634A), RBM10(NM_005676.4):c.1706T>C (p.(Val569Ala)), RBM10(NM_005676.5):c.1706T>C (p.V569A)
ISCN -
DB-ID RBM10_000035 See all 3 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) 1.0E-5 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +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.1706T>C r.(?) p.(Val569Ala)


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