Variant #0000558722 (NC_000016.9:g.67469733C>A, NM_000196.3:c.468C>A (HSD11B2))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.67469733C>A
DNA change (hg38) g.67435830C>A
Published as -
ISCN -
DB-ID ATP6V0D1_000001
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) 0.05432 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-09 17:56:32 +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.468C>A r.(?) p.(Thr156=)
ATP6V0D1 NM_004691.4 -/. - c.*2698G>T r.(=) p.(=)


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