Variant #0000119971 (NC_000005.9:g.138643318G>A)

Individual ID 00078526
Chromosome 5
Allele Parent #1
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.138643318G>A
DNA change (hg38) g.139307629G>A
Published as -
ISCN -
DB-ID MATR3_000004
Variant remarks -
Reference PubMed: Lin 2015, Journal: Lin 2015
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency 1/207 cases ALS
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Jamie Zeegers
Database submission license No license selected
Created by Jamie Zeegers
Date created 2016-07-18 13:18:31 +02:00 (CEST)
Date last edited 2018-12-27 12:16:46 +01:00 (CET)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000078701 DNA PCR;SEQ - - MATR3 1 Jamie Zeegers


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