Variant #0000168321 (NC_000017.10:g.78092158T>A, NC_000017.10(NM_000152.3):c.2646+2T>A (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.78092158T>A |
| DNA change (hg38) |
g.80118359T>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GAA_000107 See all 7 reported entries |
| Variant remarks |
predicted very severe, classic infantile phenotype when combined with null allele; predicted CRIM? (protein expression unknown) |
| Reference |
Pompe disease database 1052 |
| 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 |
2025-06-08 12:47:41 +02:00 (CEST) |

Variant on transcripts
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