17-80110708-G-A

Variant names:

• chr17-80110708-G-A
• rs2304844
• NM_000152.5:c.1438-19G>A

Variant summary

Our verdict is Likely benign. The variant received -4 ACMG points: 2P and 6B. PM2 BP4_Strong BP6_Moderate

The NM_000152.5(GAA):​c.1438-19G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000137 in 1,458,516 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★). There are indicators that this mutation may affect the branch point..

• Frequency:
  • Genomes: not found (cov: 33)
  • Exomes 𝑓: 0.0000014 (0 hom.)
• Consequence: GAA NM_000152.5 intron
• Clinical Significance: Likely benign criteria provided, single submitter B:1
• Conservation: PhyloP100: -0.190
• Publications: 0 publications found

Genes affected

GAA (HGNC:4065): (alpha glucosidase) This gene encodes lysosomal alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. The encoded preproprotein is proteolytically processed to generate multiple intermediate forms and the mature form of the enzyme. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]

GAA Gene-Disease associations (from GenCC):

• glycogen storage disease II

  Inheritance: AR Classification: DEFINITIVE, STRONG Submitted by: Genomics England PanelApp, Laboratory for Molecular Medicine, Labcorp Genetics (formerly Invitae), PanelApp Australia, ClinGen, G2P
• glycogen storage disease due to acid maltase deficiency, infantile onset

  Inheritance: AR Classification: SUPPORTIVE Submitted by: Orphanet
• glycogen storage disease due to acid maltase deficiency, late-onset

  Inheritance: AR Classification: SUPPORTIVE Submitted by: Orphanet

ACMG classification

Our verdict: Likely_benign. The variant received -4 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: This position, referring to a specific DNA site, is a probable branch point but is likely benign (scored 3 / 10, using the threshold of <=3). The score ranges from 0 to 10, with values ≤3 considered benign and >5 classified as pathogenic. Computational evidence support a benign effect (BayesDel_noAF=-0.82).
• BP6: Variant 17-80110708-G-A is Benign according to our data. Variant chr17-80110708-G-A is described in CliVar as Likely_benign. Clinvar id is 2896125.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-80110708-G-A is described in CliVar as Likely_benign. Clinvar id is 2896125.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-80110708-G-A is described in CliVar as Likely_benign. Clinvar id is 2896125.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-80110708-G-A is described in CliVar as Likely_benign. Clinvar id is 2896125.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-80110708-G-A is described in CliVar as Likely_benign. Clinvar id is 2896125.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-80110708-G-A is described in CliVar as Likely_benign. Clinvar id is 2896125.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-80110708-G-A is described in CliVar as Likely_benign. Clinvar id is 2896125.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-80110708-G-A is described in CliVar as Likely_benign. Clinvar id is 2896125.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-80110708-G-A is described in CliVar as Likely_benign. Clinvar id is 2896125.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-80110708-G-A is described in CliVar as Likely_benign. Clinvar id is 2896125.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-80110708-G-A is described in CliVar as Likely_benign. Clinvar id is 2896125.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-80110708-G-A is described in CliVar as Likely_benign. Clinvar id is 2896125.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-80110708-G-A is described in CliVar as Likely_benign. Clinvar id is 2896125.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-80110708-G-A is described in CliVar as Likely_benign. Clinvar id is 2896125.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-80110708-G-A is described in CliVar as Likely_benign. Clinvar id is 2896125.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-80110708-G-A is described in CliVar as Likely_benign. Clinvar id is 2896125.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-80110708-G-A is described in CliVar as Likely_benign. Clinvar id is 2896125.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-80110708-G-A is described in CliVar as Likely_benign. Clinvar id is 2896125.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-80110708-G-A is described in CliVar as Likely_benign. Clinvar id is 2896125.Status of the report is criteria_provided_single_submitter, 1 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
GAA	NM_000152.5	c.1438-19G>A		intron_variant	Intron 9 of 19	ENST00000302262.8	NP_000143.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
GAA	ENST00000302262.8	c.1438-19G>A		intron_variant	Intron 9 of 19	1	NM_000152.5	ENSP00000305692.3

Frequencies

GnomAD3 genomes Cov.: 33

GnomAD4 exome AF: 0.00000137 AC: 2 AN: 1458516 Hom.: 0 Cov.: 33 AF XY: 0.00000138 AC XY: 1 AN XY: 725702

African (AFR) AF: 0.00 AC: 0 AN: 33418

American (AMR) AF: 0.00 AC: 0 AN: 44690

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 26108

East Asian (EAS) AF: 0.0000252 AC: 1 AN: 39684

South Asian (SAS) AF: 0.00 AC: 0 AN: 86186

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 53128

Middle Eastern (MID) AF: 0.000187 AC: 1 AN: 5336

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 1109704

Other (OTH) AF: 0.00 AC: 0 AN: 60262

GnomAD4 genome Cov.: 33

ClinVar

Significance: Likely benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

Glycogen storage disease, type II Benign:1

Nov 24, 2023

Labcorp Genetics (formerly Invitae), Labcorp

Significance: Likely benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.82
CADD	Benign	4.9
DANN	Benign	0.56
PhyloP100		-0.19
BranchPoint Hunter		3.0
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.1

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs2304844; hg19: chr17-78084507;