Variant #0000539933 (NC_000010.10:g.48389409_48389410dup, NM_002900.2:c.1470_1471dup (RBP3))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.48389409_48389410dup
DNA change (hg38) g.47349952_47349953dup
Published as RBP3(NM_002900.3):c.1470_1471dupCC (p.L491Pfs*76)
ISCN -
DB-ID RBP3_000073
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RBP3 NM_002900.2 +?/. - c.1470_1471dup r.(?) p.(Leu491ProfsTer76)


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