Variant #0000168299 (NC_000017.10:g.78078764_78078765del, NM_000152.3:c.379_380del (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.78078764_78078765del |
| DNA change (hg38) |
g.80104965_80104966del |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GAA_000062 See all 6 reported entries |
| Variant remarks |
predicted very severe, classic infantile phenotype when combined with null allele; predicted CRIM- (no endogenous protein on Western blot) |
| Reference |
Pompe disease database 601 |
| 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 |
Marianne Hoogeveen-Westerveld |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2017-04-14 13:18:39 +02:00 (CEST) |
| Date last edited |
2019-06-28 11:29:39 +02:00 (CEST) |

Variant on transcripts
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