Variant #0000860320 (NC_000006.11:g.33170803A>G, NM_021976.4:c.-2550T>C (RXRB))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.33170803A>G
DNA change (hg38) -
Published as SLC39A7(NM_006979.3):c.1057A>G (p.M353V)
ISCN -
DB-ID HSD17B8_000009
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) 0.00121 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC39A7 NM_006979.2 -?/. - c.1057A>G r.(?) p.(Met353Val)
HSD17B8 NM_014234.4 -?/. - c.-1643A>G r.(?) p.(=)
RXRB NM_021976.4 -?/. - c.-2550T>C r.(?) p.(=)


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