Variant #0000168224 (NC_000017.10:g.78087149C>T, NM_000152.3:c.2173C>T (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.78087149C>T |
DNA change (hg38) |
g.80113350C>T |
Published as |
- |
ISCN |
- |
DB-ID |
GAA_000023 See all 8 reported entries |
Variant remarks |
predicted less severe phenotype, childhood/adult phenotype when combined with null allele; predicted CRIM+ (protein expressed); Align GVGD class C0 (GV: 127.11-GD: 65.28), SIFT deleterious (score: 0.01), Mutation Taster disease causing (p-value: 1) |
Reference |
Pompe disease database 981 |
ClinVar ID |
- |
dbSNP ID |
rs121907938 |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
MAF <0.01 |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
4.0E-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 14:08:11 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|