Variant #0000371877 (NC_000012.11:g.102179792T>A, NM_024312.4:c.569A>T (GNPTAB))
Chromosome |
12 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.102179792T>A |
DNA change (hg38) |
g.101786014T>A |
Published as |
- |
ISCN |
- |
DB-ID |
GNPTAB_000087 See all 2 reported entries |
Variant remarks |
Splicing defect or p.Asp190Val |
Reference |
Journal: Kudo 2006 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline/De novo (untested) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0 View details |
Owner |
Renata Voltolini Velho |
Database submission license |
No license selected |
Created by |
Renata Voltolini Velho |
Date created |
2018-07-09 10:25:58 +02:00 (CEST) |
Date last edited |
2019-01-15 12:47:24 +01:00 (CET) |

Variant on transcripts
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