Variant #0000168268 (NC_000017.10:g.78086713G>A, NM_000152.3:c.1927G>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.78086713G>A |
DNA change (hg38) |
g.80112914G>A |
Published as |
- |
ISCN |
- |
DB-ID |
GAA_000021 See all 24 reported entries |
Variant remarks |
predicted potentially less severe, classic infantile phenotype when combined with null allele; predicted CRIM? (protein expression unknown); Align GVGD class C65 (GV: 0.00-GD: 125.13), SIFT deleterious (score: 0), Mutation Taster disease causing (p-value: 1) |
Reference |
Pompe disease database 932 |
ClinVar ID |
- |
dbSNP ID |
rs28937909 |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
MAF <0.01 |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
3.0E-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 |
2025-06-08 16:55:45 +02:00 (CEST) |

Variant on transcripts
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