Variant #0001046992 (NC_000005.9:g.125446826T>C)

Individual ID 00466059
Chromosome 5
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.125446826T>C
DNA change (hg38) g.126111133T>C
Published as -
ISCN -
DB-ID chr5_007765
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation -
Frequency 1/12
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 2025-07-21 09:20:51 +02:00 (CEST)
Date last edited 2025-08-18 14:03:24 +02:00 (CEST)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

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Variants found     

Owner     
0000467714 DNA MS;SEQ-NG-I blood WGS - 3 Larry Baum


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