Variant #0000404766 (NC_000012.11:g.102183715C>T, NC_000012.11(NM_024312.4):c.323+1G>A (GNPTAB))
Chromosome |
12 |
Allele |
Parent #2 |
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.102183715C>T |
DNA change (hg38) |
g.101789937C>T |
Published as |
- |
ISCN |
- |
DB-ID |
GNPTAB_000285 |
Variant remarks |
- |
Reference |
- |
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 |
2018-08-26 17:44:57 +02:00 (CEST) |
Date last edited |
2019-01-14 17:14:58 +01:00 (CET) |

Variant on transcripts
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