Variant #0000478673 (NC_000017.10:g.78078417G>A, NM_000152.3:c.32G>A (GAA))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.78078417G>A |
| DNA change (hg38) |
g.80104618G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GAA_000365 See all 5 reported entries |
| Variant remarks |
predicted non-pathogenic, unknown phenotype when combined with null allele; predicted CRIM+ (protein expressed); Align GVGD class C0 (GV: 353.86-GD: 0.00), SIFT tolerated (score: 0.65), Mutation Taster polymorphism (p-value: 1) |
| Reference |
Pompe disease database 1075 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
MAF <0.01 |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00013 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
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