chr6-160027232-A-G
Variant summary
Our verdict is Benign. Variant got -14 ACMG points: 0P and 14B. BP4_StrongBP6_ModerateBS1BS2
The NM_000876.4(IGF2R):c.694A>G(p.Thr232Ala) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00132 in 1,614,222 control chromosomes in the GnomAD database, including 18 homozygotes. In-silico tool predicts a benign outcome for this variant. 13/19 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).
Frequency
Genomes: 𝑓 0.0065 ( 5 hom., cov: 33)
Exomes 𝑓: 0.00078 ( 13 hom. )
Consequence
IGF2R
NM_000876.4 missense
NM_000876.4 missense
Scores
16
Clinical Significance
Conservation
PhyloP100: 1.48
Genes affected
IGF2R (HGNC:5467): (insulin like growth factor 2 receptor) This gene encodes a receptor for both insulin-like growth factor 2 and mannose 6-phosphate. The binding sites for each ligand are located on different segments of the protein. This receptor has various functions, including in the intracellular trafficking of lysosomal enzymes, the activation of transforming growth factor beta, and the degradation of insulin-like growth factor 2. Mutation or loss of heterozygosity of this gene has been association with risk of hepatocellular carcinoma. The orthologous mouse gene is imprinted and shows exclusive expression from the maternal allele; however, imprinting of the human gene may be polymorphic, as only a minority of individuals showed biased expression from the maternal allele (PMID:8267611). [provided by RefSeq, Nov 2015]
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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 (MetaRNN=0.013038099).
BP6
?
Variant 6-160027232-A-G is Benign according to our data. Variant chr6-160027232-A-G is described in ClinVar as [Benign]. Clinvar id is 789187.Status of the report is criteria_provided_single_submitter, 1 stars.
BS1
?
Variant frequency is greater than expected in population afr. gnomad4 allele frequency = 0.00653 (995/152348) while in subpopulation AFR AF= 0.0221 (917/41576). AF 95% confidence interval is 0.0209. There are 5 homozygotes in gnomad4. There are 480 alleles in male gnomad4 subpopulation. Median coverage is 33. This position pass quality control queck.
BS2
?
High AC in GnomAd at 994 AD gene.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
IGF2R | NM_000876.4 | c.694A>G | p.Thr232Ala | missense_variant | 6/48 | ENST00000356956.6 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
IGF2R | ENST00000356956.6 | c.694A>G | p.Thr232Ala | missense_variant | 6/48 | 1 | NM_000876.4 | P1 | |
IGF2R | ENST00000677704.1 | c.694A>G | p.Thr232Ala | missense_variant, NMD_transcript_variant | 6/49 | ||||
IGF2R | ENST00000676781.1 | c.694A>G | p.Thr232Ala | missense_variant, NMD_transcript_variant | 6/49 |
Frequencies
GnomAD3 genomes ? AF: 0.00653 AC: 994AN: 152230Hom.: 5 Cov.: 33
GnomAD3 genomes
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GnomAD3 exomes AF: 0.00172 AC: 433AN: 251266Hom.: 6 AF XY: 0.00135 AC XY: 183AN XY: 135866
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GnomAD4 exome AF: 0.000780 AC: 1140AN: 1461874Hom.: 13 Cov.: 31 AF XY: 0.000664 AC XY: 483AN XY: 727238
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267
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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 | Invitae | Jul 23, 2018 | - - |
Computational scores
Source:
Name
Calibrated prediction
Score
Prediction
AlphaMissense
Benign
BayesDel_addAF
Benign
T
BayesDel_noAF
Benign
Cadd
Benign
Dann
Benign
DEOGEN2
Benign
T;T
Eigen
Benign
Eigen_PC
Benign
FATHMM_MKL
Benign
D
MetaRNN
Benign
T;T
MetaSVM
Benign
T
MutationTaster
Benign
N
PrimateAI
Benign
T
PROVEAN
Benign
N;.
REVEL
Benign
Sift
Benign
T;.
Sift4G
Benign
T;.
Polyphen
B;B
Vest4
MVP
MPC
ClinPred
T
GERP RS
RBP_binding_hub_radar
RBP_regulation_power_radar
Varity_R
gMVP
Splicing
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SpliceAI score (max)
Details are displayed if max score is > 0.2
Find out detailed SpliceAI scores and Pangolin per-transcript scores at