Variant #0000528682 (NC_000006.11:g.33173607A>G, NM_021976.4:c.-5354T>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.33173607A>G
DNA change (hg38) g.33205830A>G
Published as HSD17B8(NM_014234.4):c.569A>G (p.(His190Arg))
ISCN -
DB-ID HSD17B8_000002
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) 0.00258 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RING1 NM_002931.3 -?/. - c.-2873A>G r.(?) p.(=)
SLC39A7 NM_006979.2 -?/. - c.*2017A>G r.(=) p.(=)
HSD17B8 NM_014234.4 -?/. - c.569A>G r.(?) p.(His190Arg)
RXRB NM_021976.4 -?/. - c.-5354T>C r.(?) p.(=)


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