Variant #0000720893 (NC_000006.11:g.33169688T>A, NM_021976.4:c.-1435A>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.33169688T>A
DNA change (hg38) -
Published as SLC39A7(NM_006979.3):c.578T>A (p.L193H)
ISCN -
DB-ID HSD17B8_000005 See all 2 reported entries
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) 3.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC39A7 NM_006979.2 ?/. - c.578T>A r.(?) p.(Leu193His)
HSD17B8 NM_014234.4 ?/. - c.-2758T>A r.(?) p.(=)
RXRB NM_021976.4 ?/. - c.-1435A>T r.(?) p.(=)


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