Variant #0000991659 (NC_000002.11:g.149247783C>A, NM_181742.3:c.-468784G>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.149247783C>A
DNA change (hg38) g.148490214C>A
Published as MBD5(NM_018328.4):c.3883C>A (p.(Pro1295Thr))
ISCN -
DB-ID MBD5_000112
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 2024-08-28 13:07:21 +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.4582C>A r.(?) p.(Pro1528Thr)
ORC4 NM_181742.3 ?/. - c.-468784G>T r.(?) p.(=)


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