rs387906246

Variant names:

• chr1-99881174-TC-T
• rs387906246
• NM_000642.3:c.1999delC

Variant summary

Our verdict is Pathogenic. The variant received 11 ACMG points: 11P and 0B. PVS1 PM2 PP5

The NM_000642.3(AGL):​c.1999delC​(p.Gln667ArgfsTer63) variant causes a frameshift, splice region change involving the alteration of a conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. Variant has been reported in ClinVar as Pathogenic (no stars). Variant results in nonsense mediated mRNA decay.

• Frequency: Genomes: not found (cov: 32)
• Consequence: AGL NM_000642.3 frameshift, splice_region
• Clinical Significance: Pathogenic no assertion criteria provided P:1
• Conservation: PhyloP100: 7.47
• Publications: 1 publications found

Genes affected

AGL (HGNC:321): (amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase) This gene encodes the glycogen debrancher enzyme which is involved in glycogen degradation. This enzyme has two independent catalytic activities which occur at different sites on the protein: a 4-alpha-glucotransferase activity and a amylo-1,6-glucosidase activity. Mutations in this gene are associated with glycogen storage disease although a wide range of enzymatic and clinical variability occurs which may be due to tissue-specific alternative splicing. Alternatively spliced transcripts encoding different isoforms have been described. [provided by RefSeq, Jul 2008]

AGL Gene-Disease associations (from GenCC):

• glycogen storage disease III

  Inheritance: AR Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: ClinGen, Ambry Genetics, Laboratory for Molecular Medicine, Myriad Women’s Health, Orphanet, G2P, PanelApp Australia, Labcorp Genetics (formerly Invitae), Genomics England PanelApp

ACMG classification

Our verdict: Pathogenic. The variant received 11 ACMG points.

• PVS1: Loss of function variant, product undergoes nonsense mediated mRNA decay. LoF is a known mechanism of disease.
• PM2: Very rare variant in population databases, with high coverage
• PP5: Variant 1-99881174-TC-T is Pathogenic according to our data. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr1-99881174-TC-T is described in CliVar as Pathogenic. Clinvar id is 1104.Status of the report is no_assertion_criteria_provided, 0 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
AGL	NM_000642.3	c.1999delC	p.Gln667ArgfsTer63	frameshift_variant, splice_region_variant	Exon 15 of 34	ENST00000361915.8	NP_000633.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
AGL	ENST00000361915.8	c.1999delC	p.Gln667ArgfsTer63	frameshift_variant, splice_region_variant	Exon 15 of 34	1	NM_000642.3	ENSP00000355106.3

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 31

GnomAD4 genome Cov.: 32

ClinVar

Significance: Pathogenic

Submissions summary: Pathogenic:1

Revision: no assertion criteria provided

Submissions by phenotype

Glycogen storage disease IIIb Pathogenic:1

Jul 31, 2000

OMIM

Significance: Pathogenic

Review Status: no assertion criteria provided

Collection Method: literature only

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Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
PhyloP100		7.5
Mutation Taster		=0/200	disease causing (ClinVar)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.34		Details are displayed if max score is > 0.2
DS_DL_spliceai		0.34		Position offset: 3

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

Other links and lift over

dbSNP: rs387906246; hg19: chr1-100346730;