Variant #0000885707 (NC_000003.11:g.25686916T>C, NM_000965.3:c.*48809T>C (RARB))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.25686916T>C
DNA change (hg38) -
Published as TOP2B(NM_001068.3):c.100A>G (p.T34A)
ISCN -
DB-ID RARB_000037
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 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +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     
RARB NM_000965.3 -?/. - c.*48809T>C r.(=) p.(=)
TOP2B NM_001068.2 -?/. - c.100A>G r.(?) p.(Thr34Ala)


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