Variant #0001046907 (NC_000015.9:g.93777067G>A)

Individual ID 00466039
Chromosome 15
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.93777067G>A
DNA change (hg38) g.93233838G>A
Published as -
ISCN -
DB-ID chr15_006375
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation -
Frequency -
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 09:44:21 +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     
0000467692 DNA MS;SEQ-NG-I blood - - 6 Larry Baum


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