Variant #0000800382 (NC_000002.11:g.219647128C>G, NM_000784.3:c.223C>G (CYP27A1))

Chromosome 2
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.219647128C>G
DNA change (hg38) -
Published as CYP27A1(NM_000784.3):c.223C>G (p.Q75E), CYP27A1(NM_000784.4):c.223C>G (p.Q75E)
ISCN -
DB-ID CYP27A1_000236 See all 2 reported entries
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
CYP27A1 NM_000784.3 -?/. - c.223C>G r.(?) p.(Gln75Glu) -


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