Variant #0000518954 (NC_000003.11:g.25678716C>T, NM_000965.3:c.*40609C>T (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.25678716C>T
DNA change (hg38) g.25637225C>T
Published as TOP2B(NM_001068.3):c.614G>A (p.(Ser205Asn))
ISCN -
DB-ID RARB_000011
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) 0.00028 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +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.*40609C>T r.(=) p.(=)
TOP2B NM_001068.2 -?/. - c.614G>A r.(?) p.(Ser205Asn)


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