Variant #0000168273 (NC_000017.10:g.78082197T>C, NM_000152.3:c.1064T>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.78082197T>C |
DNA change (hg38) |
g.80108398T>C |
Published as |
- |
ISCN |
- |
DB-ID |
GAA_000129 See all 18 reported entries |
Variant remarks |
predicted potentially less severe, classic infantile/childhood phenotype when combined with null allele; predicted CRIM+ (endogenous protein on Western blot) ; Align GVGD class C0 (GV: 120.48-GD: 28.88), SIFT tolerated (score: 0.08), Mutation Taster disease causing (p-value: 1) |
Reference |
Pompe disease database 715 |
ClinVar ID |
- |
dbSNP ID |
rs766074609 |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
MAF <0.01 |
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 |
2025-03-15 10:41:21 +01:00 (CET) |

Variant on transcripts
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