Variant #0000713237 (NC_000017.10:g.38510572C>T, NM_000964.3:c.826C>T (RARA))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.38510572C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID RARA_000001 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs786205678
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 2021-01-27 09:36:02 +01:00 (CET)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RARA NM_000964.3 +/. - c.826C>T r.(?) p.(Arg276Trp)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.