Variant #0000351338 (NC_000016.9:g.67470294G>C, NC_000016.9(NM_000196.3):c.802+5G>C (HSD11B2))

Chromosome 16
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.67470294G>C
DNA change (hg38) g.67436391G>C
Published as -
ISCN -
DB-ID HSD11B2_000007
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) 0.00024 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-09 17:57:12 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSD11B2 NM_000196.3 ?/. - c.802+5G>C r.spl? p.?
ATP6V0D1 NM_004691.4 ?/. - c.*2137C>G r.(=) p.(=)


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