Variant #0000369809 (NC_000016.9:g.1412038G>C, NC_000016.9(NM_032520.4):c.318-1G>C (GNPTG))
Chromosome |
16 |
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.1412038G>C |
DNA change (hg38) |
g.1362037G>C |
Published as |
IVS5-1G>C |
ISCN |
- |
DB-ID |
GNPTG_000050 See all 2 reported entries |
Variant remarks |
- |
Reference |
Journal: Raas-Rothschild 2004 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
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 |
2018-06-26 14:47:17 +02:00 (CEST) |
Date last edited |
2020-07-07 12:46:17 +02:00 (CEST) |

Variant on transcripts
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