Variant #0000300535 (NC_000001.10:g.52854961G>A, NM_004153.3:c.1115C>T (ORC1))

Chromosome 1
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.52854961G>A
DNA change (hg38) g.52389289G>A
Published as ORC1(NM_001190818.1):c.1115C>T (p.(Ala372Val)), ORC1(NM_004153.4):c.1115C>T (p.A372V)
ISCN -
DB-ID ORC1_000005 See all 3 reported entries
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) 0.01508 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ORC1 NM_004153.3 -?/. - c.1115C>T r.(?) p.(Ala372Val)


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