Variant #0000955104 (NC_000003.11:g.25635051G>A, NM_000965.3:c.844G>A (RARB))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.25635051G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID RARB_000047
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1553637463
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-01-05 16:26:01 +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.844G>A r.(?) p.(Gly282Ser)


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