chr11-74346602-T-C
Variant summary
Our verdict is Benign. Variant got -14 ACMG points: 0P and 14B. BP4_StrongBP6_ModerateBA1
The NM_173582.6(PGM2L1):c.1037+130A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.632 in 633,872 control chromosomes in the GnomAD database, including 128,545 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).
Frequency
Genomes: 𝑓 0.60 ( 27739 hom., cov: 32)
Exomes 𝑓: 0.64 ( 100806 hom. )
Consequence
PGM2L1
NM_173582.6 intron
NM_173582.6 intron
Scores
2
Clinical Significance
Conservation
PhyloP100: -0.285
Genes affected
PGM2L1 (HGNC:20898): (phosphoglucomutase 2 like 1) Enables glucose-1,6-bisphosphate synthase activity. Predicted to be involved in glucose metabolic process and phosphorylation. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Apr 2022]
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ACMG classification
Classification made for transcript
Verdict is Benign. Variant got -14 ACMG points.
BP4
?
Computational evidence support a benign effect (BayesDel_noAF=-0.92).
BP6
?
Variant 11-74346602-T-C is Benign according to our data. Variant chr11-74346602-T-C is described in ClinVar as [Benign]. Clinvar id is 1294901.Status of the report is criteria_provided_single_submitter, 1 stars.
BA1
?
GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.783 is higher than 0.05.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
PGM2L1 | NM_173582.6 | c.1037+130A>G | intron_variant | ENST00000298198.5 | |||
LOC112268078 | XR_002957258.2 | n.314+17114T>C | intron_variant, non_coding_transcript_variant | ||||
PGM2L1 | XM_011544953.4 | c.1100+130A>G | intron_variant |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
PGM2L1 | ENST00000298198.5 | c.1037+130A>G | intron_variant | 1 | NM_173582.6 | P1 |
Frequencies
GnomAD3 genomes ? AF: 0.596 AC: 90631AN: 151944Hom.: 27731 Cov.: 32
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GnomAD4 exome AF: 0.643 AC: 309890AN: 481810Hom.: 100806 AF XY: 0.642 AC XY: 162359AN XY: 252898
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GnomAD4 genome ? AF: 0.596 AC: 90669AN: 152062Hom.: 27739 Cov.: 32 AF XY: 0.603 AC XY: 44853AN XY: 74346
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ClinVar
Significance: Benign
Submissions summary: Benign:1
Revision: criteria provided, single submitter
LINK: link
Submissions by phenotype
not provided Benign:1
Benign, criteria provided, single submitter | clinical testing | GeneDx | May 14, 2021 | - - |
Computational scores
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BayesDel_noAF
Benign
Cadd
Benign
Dann
Benign
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Details are displayed if max score is > 0.2
Find out detailed SpliceAI scores and Pangolin per-transcript scores at