Variant #0000669663 (NC_000020.10:g.18513350G>A, SEC23B(NM_032985.4):c.1276G>A)

Individual ID 00304846
Chromosome 20
Allele Both (homozygous)
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.18513350G>A
DNA change (hg38) g.18532706G>A
Published as -
ISCN -
DB-ID SEC23B_000011 See all 4 reported entries
Variant remarks 3 homozygous; Clinindb (India)
Reference PubMed: Narang 2020, Journal: Narang 2020
ClinVar ID -
dbSNP ID rs41309927
Origin Germline
Segregation -
Frequency 3/2795 individuals
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.04318 View details
Owner Mohammed Faruq
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SEC23B NM_032985.4 -?/. - c.1276G>A r.(?) p.(Val426Ile)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000305975 DNA arraySNP - Infinium Global Screening Array v1.0 - 1 Mohammed Faruq