Variant #0000478603 (NC_000017.10:g.78087111T>C, NM_000152.3:c.2135T>C (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.78087111T>C |
| DNA change (hg38) |
g.80113312T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GAA_000330 See all 4 reported entries |
| Variant remarks |
predicted less severe phenotype, unknown (disease-associated) phenotype when combined with null allele; predicted CRIM+ (protein expressed); Align GVGD class C45 (GV: 14.30-GD: 86.59), SIFT deleterious (score: 0), Mutation Taster disease causing (p-value: 1) |
| Reference |
Pompe disease database 974 |
| 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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