Variant #0000802555 (NC_000006.11:g.33169186A>G, NM_021976.4:c.-933T>C (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.33169186A>G
DNA change (hg38) -
Published as SLC39A7(NM_006979.3):c.164A>G (p.H55R)
ISCN -
DB-ID HSD17B8_000006
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +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.164A>G r.(?) p.(His55Arg)
HSD17B8 NM_014234.4 ?/. - c.-3260A>G r.(?) p.(=)
RXRB NM_021976.4 ?/. - c.-933T>C r.(?) p.(=)


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