Variant #0000717243 (NC_000001.10:g.228437717C>T, NM_001271223.2:c.4361C>T (OBSCN))

Chromosome 1
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.228437717C>T
DNA change (hg38) -
Published as OBSCN(NM_001271223.2):c.4361C>T (p.A1454V), OBSCN(NM_052843.4):c.4085C>T (p.A1362V)
ISCN -
DB-ID OBSCN_000103 See all 2 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) 0.00041 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2025-07-08 13:22:38 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OBSCN NM_001271223.2 ?/. - c.4361C>T r.(?) p.(Ala1454Val)


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