Variant #0000677758 (NC_000006.11:g.33170729C>T, NM_021976.4:c.-2476G>A (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.33170729C>T
DNA change (hg38) -
Published as SLC39A7(NM_006979.3):c.983C>T (p.A328V)
ISCN -
DB-ID HSD17B8_000004
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) 6.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +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.983C>T r.(?) p.(Ala328Val)
HSD17B8 NM_014234.4 ?/. - c.-1717C>T r.(?) p.(=)
RXRB NM_021976.4 ?/. - c.-2476G>A r.(?) p.(=)


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