Variant #0000763597 (NC_000011.9:g.64519395C>T, NC_000011.9(NM_005609.2):c.1768+1G>A (PYGM))
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.64519395C>T |
| DNA change (hg38) |
g.64751923C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
PYGM_000010 See all 5 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
2.0E-5 View details |
| Owner |
Irene Vieitez |
| Database submission license |
No license selected |
| Created by |
Irene Vieitez |
| Date created |
2021-04-12 14:00:11 +02:00 (CEST) |
| Date last edited |
2021-04-12 14:01:18 +02:00 (CEST) |

Variant on transcripts
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