Variant #0000923293 (NC_000002.11:g.149226529del, NM_181742.3:c.-447530del (ORC4))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.149226529del
DNA change (hg38) g.148468960del
Published as -
ISCN -
DB-ID MBD5_000092
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited 2024-10-29 20:49:11 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MBD5 NM_001378120.1 +?/. - c.1017del r.(?) p.(Pro340Leufs*12)
ORC4 NM_181742.3 +?/. - c.-447530del r.(?) p.(=)


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