Variant #0000320837 (NC_000001.10:g.55337168G>A, DHCR24(NM_014762.3):c.731C>T)

Chromosome 1
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.55337168G>A
DNA change (hg38) g.54871495G>A
Published as DHCR24(NM_014762.3):c.731C>T (p.(Pro244Leu))
ISCN -
DB-ID DHCR24_000004
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00058 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DHCR24 NM_014762.3 ?/. - c.731C>T r.(?) p.(Pro244Leu)