Variant #0000168318 (NC_000017.10:g.78091658_78092195del, NC_000017.10(NM_000152.3):c.2481+110_2646+39del (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.78091658_78092195del |
DNA change (hg38) |
g.80117859_80118396del |
Published as |
- |
ISCN |
- |
DB-ID |
GAA_000037 See all 34 reported entries |
Variant remarks |
predicted very severe, classic infantile phenotype when combined with null allele; predicted CRIM+ (endogenous protein on Western blot) |
Reference |
Pompe disease database 1039 |
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 |
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 07:34:00 +02:00 (CEST) |

Variant on transcripts
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