Variant #0000923292 (NC_000002.11:g.149221350G>T, NM_181742.3:c.-442351C>A (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.149221350G>T
DNA change (hg38) g.148463781G>T
Published as MBD5(NM_018328.5):c.259G>T (p.A87S)
ISCN -
DB-ID MBD5_000091
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) 0 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 2023-04-16 21:50:28 +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.259G>T r.(?) p.(Ala87Ser)
ORC4 NM_181742.3 ?/. - c.-442351C>A r.(?) p.(=)


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