Variant #0000995725 (NC_000006.11:g.33168235G>A, NM_021976.4:c.19C>T (RXRB))

Chromosome 6
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.33168235G>A
DNA change (hg38) -
Published as RXRB(NM_001270401.1):c.19C>T (p.(Pro7Ser))
ISCN -
DB-ID HSD17B8_000012
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC39A7 NM_006979.2 ?/. - c.-788G>A r.(?) p.(=)
HSD17B8 NM_014234.4 ?/. - c.-4211G>A r.(?) p.(=)
RXRB NM_021976.4 ?/. - c.19C>T r.(?) p.(Pro7Ser)


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