Variant #0001050816 (NC_000002.11:g.149241116T>A, NM_181742.3:c.-462117A>T (ORC4))

Chromosome 2
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.149241116T>A
DNA change (hg38) -
Published as MBD5(NM_001378120.1):c.2956T>A (p.(Phe986Ile))
ISCN -
DB-ID ORC4_000018
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +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     
MBD5 NM_001378120.1 ?/. - c.2956T>A r.(?) p.(Phe986Ile)
ORC4 NM_181742.3 ?/. - c.-462117A>T r.(?) p.(=)


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