Variant #0000893109 (NC_000016.9:g.67470505G>A, NM_000196.3:c.817G>A (HSD11B2))

Chromosome 16
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.67470505G>A
DNA change (hg38) -
Published as HSD11B2(NM_000196.4):c.817G>A (p.V273M)
ISCN -
DB-ID ATP6V0D1_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) 0.00139 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSD11B2 NM_000196.3 -?/. - c.817G>A r.(?) p.(Val273Met)
ATP6V0D1 NM_004691.4 -?/. - c.*1926C>T r.(=) p.(=)


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