Variant #0001032389 (NC_000002.11:g.149241268G>T, NM_181742.3:c.-462269C>A (ORC4))

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.149241268G>T
DNA change (hg38) -
Published as MBD5(NM_001378120.1):c.3108G>T (p.(Leu1036Phe))
ISCN -
DB-ID ORC4_000014
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 2025-05-05 21:14:00 +02:00 (CEST)
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.3108G>T r.(?) p.(Leu1036Phe)
ORC4 NM_181742.3 -?/. - c.-462269C>A r.(?) p.(=)


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