Variant #0001070734 (NC_000005.9:g.74650427C>T, NM_000859.2:c.1468C>T (HMGCR))

Chromosome 5
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.74650427C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID HMGCR_000014
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1277575286
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-03-13 16:18:01 +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     
HMGCR NM_000859.2 ?/. - c.1468C>T r.(?) p.(Arg490Cys)


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