Variant #0000168222 (NC_000017.10:g.78086420C>T, NM_000152.3:c.1798C>T (GAA))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.78086420C>T |
| DNA change (hg38) |
g.80112621C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GAA_000092 See all 14 reported entries |
| Variant remarks |
predicted less severe phenotype, classic infantile phenotype when combined with null allele; predicted CRIM+ (protein expressed); Align GVGD class C65 (GV: 0.00-GD: 179.53), SIFT deleterious (score: 0), Mutation Taster disease causing (p-value: 1) |
| Reference |
Pompe disease database 896 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
MAF not reported |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
| 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 |
2025-03-12 19:16:16 +01:00 (CET) |

Variant on transcripts
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