Variant #0000478291 (NC_000017.10:g.78084525G>C, NC_000017.10(NM_000152.3):c.1438-1G>C (GAA))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.78084525G>C |
| DNA change (hg38) |
g.80110726G>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GAA_000096 See all 4 reported entries |
| Variant remarks |
predicted very severe, unknown (disease-associated) phenotype when combined with null allele; predicted CRIM? (protein expression unknown) |
| Reference |
Pompe disease database 802 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
MAF not reported |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Pim Pijnappel |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2019-05-09 16:06:10 +02:00 (CEST) |
| Date last edited |
2020-07-14 14:26:09 +02:00 (CEST) |

Variant on transcripts
|