chr11-74346886-C-T
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Variant summary
Our verdict is Benign. Variant got -14 ACMG points: 0P and 14B. BP4_StrongBP6_ModerateBA1
The NM_173582.6(PGM2L1):c.940-57G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.623 in 1,329,062 control chromosomes in the GnomAD database, including 264,319 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).
Frequency
Genomes: 𝑓 0.54 ( 24612 hom., cov: 31)
Exomes 𝑓: 0.63 ( 239707 hom. )
Consequence
PGM2L1
NM_173582.6 intron
NM_173582.6 intron
Scores
2
Clinical Significance
Conservation
PhyloP100: -0.334
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=-0.93).
BP6
Variant 11-74346886-C-T is Benign according to our data. Variant chr11-74346886-C-T is described in ClinVar as [Benign]. Clinvar id is 1241016.Status of the report is criteria_provided_single_submitter, 1 stars.
BA1
GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.785 is higher than 0.05.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
PGM2L1 | NM_173582.6 | c.940-57G>A | intron_variant | ENST00000298198.5 | |||
LOC112268078 | XR_002957258.2 | n.314+17398C>T | intron_variant, non_coding_transcript_variant | ||||
PGM2L1 | XM_011544953.4 | c.1003-57G>A | intron_variant |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
PGM2L1 | ENST00000298198.5 | c.940-57G>A | intron_variant | 1 | NM_173582.6 | P1 |
Frequencies
GnomAD3 genomes AF: 0.542 AC: 82319AN: 151868Hom.: 24602 Cov.: 31
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GnomAD4 exome AF: 0.634 AC: 745686AN: 1177076Hom.: 239707 AF XY: 0.634 AC XY: 379960AN XY: 598984
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GnomAD4 genome AF: 0.542 AC: 82353AN: 151986Hom.: 24612 Cov.: 31 AF XY: 0.552 AC XY: 40985AN XY: 74266
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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