Variant #0000163053 (NC_000002.11:g.55910954G>A, NM_033109.4:c.419C>T (PNPT1))
| Chromosome |
2 |
| Allele |
Unknown |
| 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.55910954G>A |
| DNA change (hg38) |
g.55683819G>A |
| Published as |
g.55910954C>T |
| ISCN |
- |
| DB-ID |
PNPT1_000002 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
2.0E-5 View details |
| Owner |
Sanna Matilainen |
| Database submission license |
No license selected |
| Created by |
Sanna Matilainen |
| Date created |
2017-02-10 15:27:25 +01:00 (CET) |
| Date last edited |
2017-02-19 11:22:36 +01:00 (CET) |

Variant on transcripts
Screenings
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