Variant #0000851198 (NC_000006.11:g.33177709C>T, NM_014234.4:c.*3278C>T (HSD17B8))

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.33177709C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID HSD17B8_000010
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RING1 NM_002931.3 ?/. - c.257C>T r.(?) p.(Thr86Ile)
HSD17B8 NM_014234.4 ?/. - c.*3278C>T r.(=) p.(=)


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