Variant #0000371888 (NC_000012.11:g.102174065C>T, NC_000012.11(NM_024312.4):c.637-1G>A (GNPTAB))
Chromosome |
12 |
Allele |
Paternal (confirmed) |
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.102174065C>T |
DNA change (hg38) |
g.101780287C>T |
Published as |
- |
ISCN |
- |
DB-ID |
GNPTAB_000092 |
Variant remarks |
- |
Reference |
Journal: Cathey 2010 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Renata Voltolini Velho |
Database submission license |
No license selected |
Created by |
Renata Voltolini Velho |
Date created |
2018-07-09 15:25:41 +02:00 (CEST) |
Date last edited |
2020-07-02 17:53:46 +02:00 (CEST) |

Variant on transcripts
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