Variant #0000478699 (NC_000017.10:g.78086757G>A, NM_000152.3:c.1971G>A (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.78086757G>A |
| DNA change (hg38) |
g.80112958G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GAA_000183 See all 3 reported entries |
| Variant remarks |
predicted non-pathogenic, unknown phenotype when combined with null allele; predicted CRIM+ (protein expressed) |
| Reference |
Pompe disease database 1107 |
| 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 |
2019-06-28 11:29:39 +02:00 (CEST) |

Variant on transcripts
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