Variant #0000478552 (NC_000017.10:g.78086424C>G, NM_000152.3:c.1802C>G (GAA))
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
ACMG |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.78086424C>G |
DNA change (hg38) |
g.80112625C>G |
Published as |
- |
ISCN |
- |
DB-ID |
GAA_000412 See all 3 reported entries |
Variant remarks |
predicted potentially less severe, unknown (disease-associated) phenotype when combined with null allele; predicted CRIM+ (protein expressed); Align GVGD class C25 (GV: 99.13-GD: 146.49), SIFT deleterious (score: 0), Mutation Taster disease causing (p-value: 1) |
Reference |
Pompe disease database 900 |
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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