Variant #0000914112 (NC_000013.10:g.50121323_50121324dup, NC_000013.10(NM_018191.3):c.1045+2281_1045+2282dup (RCBTB1))

Chromosome 13
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.50121323_50121324dup
DNA change (hg38) -
Published as RCBTB1(NM_001352506.2):c.466+2281_466+2282dupTT
ISCN -
DB-ID RCBTB1_000043
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 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RCBTB1 NM_018191.3 -/. - c.1045+2281_1045+2282dup r.(=) p.(=)


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