Variant #0000928269 (NC_000002.11:g.149226746G>A, NM_181742.3:c.-447747C>T (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.149226746G>A
DNA change (hg38) g.148469177G>A
Published as MBD5(NM_018328.5):c.1234G>A (p.V412I)
ISCN -
DB-ID MBD5_000094
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) 4.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited 2024-09-06 10:57:40 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MBD5 NM_001378120.1 -?/. - c.1234G>A r.(?) p.(Val412Ile)
ORC4 NM_181742.3 -?/. - c.-447747C>T r.(?) p.(=)


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