Variant #0000478424 (NC_000017.10:g.78082104C>T, NM_000152.3:c.971C>T (GAA))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.78082104C>T |
| DNA change (hg38) |
g.80108305C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GAA_000089 See all 4 reported entries |
| Variant remarks |
predicted less severe phenotype, unknown (disease-associated) phenotype when combined with null allele; predicted CRIM+ (protein expressed); Align GVGD class C0 (GV: 107.83-GD: 63.55), SIFT deleterious (score: 0.04), Mutation Taster disease causing (p-value: 1) |
| Reference |
Pompe disease database 704 |
| ClinVar ID |
- |
| dbSNP ID |
rs750030887 |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
MAF <0.01 |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
| 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 |
2019-06-28 11:29:39 +02:00 (CEST) |

Variant on transcripts
|