Variant #0000502685 (NC_000001.10:g.119964811_119964837del, NM_000198.3:c.687_713del (HSD3B2))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.119964811_119964837del
DNA change (hg38) g.119422188_119422214del
Published as HSD3B2(NM_001166120.2):c.687_713delCTGGGCCCACATTCTGGCCTTGAGGGC (p.W230_A238del)
ISCN -
DB-ID HSD3B2_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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSD3B2 NM_000198.3 +/. - c.687_713del r.(?) p.(Trp230_Ala238del)


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