Variant #0000478647 (NC_000017.10:g.78091499del, NM_000152.3:c.2432del (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.78091499del |
DNA change (hg38) |
g.80117700del |
Published as |
- |
ISCN |
- |
DB-ID |
GAA_000167 See all 4 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 1033 |
ClinVar ID |
- |
dbSNP ID |
rs766560578 |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
MAF <0.01 |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0 View details |
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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