Variant #0001046909 (NC_000002.11:g.19340565T>A)

Individual ID 00466040
Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.19340565T>A
DNA change (hg38) g.19140804T>A
Published as -
ISCN -
DB-ID chr2_023949
Variant remarks in gene AC092594.1 or LINC01376
Reference -
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation -
Frequency 1/12 trios
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Larry Baum
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Larry Baum
Date created 2025-07-13 10:02:23 +02:00 (CEST)
Date last edited 2025-08-26 15:53:43 +02:00 (CEST)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

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Genes screened     

Variants found     

Owner     
0000467693 DNA MS;SEQ-NG-I blood - - 4 Larry Baum


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