Variant #0000323411 (NC_000013.10:g.52342400C>T, NM_024705.2:c.*860G>A (DHRS12))

Chromosome 13
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.52342400C>T
DNA change (hg38) g.51768264C>T
Published as DHRS12(NM_001270424.1):c.877G>A (p.(Ala293Thr))
ISCN -
DB-ID DHRS12_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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DHRS12 NM_024705.2 ?/. - c.*860G>A r.(=) p.(=)
WDFY2 NM_052950.3 ?/. - c.*8495C>T r.(=) p.(=)


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