Variant #0000329293 (NC_000003.11:g.25639821C>T, NM_000965.3:c.*1714C>T (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.25639821C>T
DNA change (hg38) g.25598330C>T
Published as TOP2B(NM_001068.3):c.4843G>A (p.(Val1615Ile), p.V1615I), TOP2B(NM_001330700.1):c.4858G>A (p.V1620I)
ISCN -
DB-ID TOP2B_000001 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) 0.00072 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 2018-01-15 20:58:59 +01:00 (CET)
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     
RARB NM_000965.3 ?/. - c.*1714C>T r.(=) p.(=)
TOP2B NM_001068.2 ?/. - c.4843G>A r.(?) p.(Val1615Ile)


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