Variant #0000801144 (NC_000003.11:g.25683846T>A, NM_000965.3:c.*45739T>A (RARB))

Chromosome 3
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.25683846T>A
DNA change (hg38) -
Published as TOP2B(NM_001068.3):c.347A>T (p.K116M), TOP2B(NM_001330700.2):c.362A>T (p.(Lys121Met))
ISCN -
DB-ID RARB_000028 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) 4.0E-5 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RARB NM_000965.3 ?/. - c.*45739T>A r.(=) p.(=)
TOP2B NM_001068.2 ?/. - c.347A>T r.(?) p.(Lys116Met)


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