3-37004444-C-T
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Variant summary
Our verdict is Pathogenic. Variant got 12 ACMG points: 12P and 0B. PM5PP3_ModeratePP5_Very_Strong
The NM_000249.4(MLH1):c.350C>T(p.Thr117Met) variant causes a missense change. The variant allele was found at a frequency of 0.00000821 in 1,461,766 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a pathogenic outcome for this variant. Variant has been reported in ClinVar as Pathogenic (★★★). Another variant affecting the same amino acid position, but resulting in a different missense (i.e. T117R) has been classified as Pathogenic.
Frequency
Genomes: not found (cov: 33)
Exomes 𝑓: 0.0000082 ( 0 hom. )
Consequence
MLH1
NM_000249.4 missense
NM_000249.4 missense
Scores
17
1
1
Clinical Significance
Conservation
PhyloP100: 5.83
Genes affected
MLH1 (HGNC:7127): (mutL homolog 1) The protein encoded by this gene can heterodimerize with mismatch repair endonuclease PMS2 to form MutL alpha, part of the DNA mismatch repair system. When MutL alpha is bound by MutS beta and some accessory proteins, the PMS2 subunit of MutL alpha introduces a single-strand break near DNA mismatches, providing an entry point for exonuclease degradation. The encoded protein is also involved in DNA damage signaling and can heterodimerize with DNA mismatch repair protein MLH3 to form MutL gamma, which is involved in meiosis. This gene was identified as a locus frequently mutated in hereditary nonpolyposis colon cancer (HNPCC). [provided by RefSeq, Aug 2017]
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ACMG classification
Classification made for transcript
Verdict is Pathogenic. Variant got 12 ACMG points.
PM5
Other missense variant is known to change same aminoacid residue: Variant chr3-37004444-C-G is described in Lovd as [Pathogenic].
PP3
MetaRNN computational evidence supports a deleterious effect, 0.912
PP5
Variant 3-37004444-C-T is Pathogenic according to our data. Variant chr3-37004444-C-T is described in ClinVar as [Pathogenic]. Clinvar id is 17094.Status of the report is reviewed_by_expert_panel, 3 stars. Variant chr3-37004444-C-T is described in Lovd as [Pathogenic]. Variant chr3-37004444-C-T is described in Lovd as [Benign]. Variant chr3-37004444-C-T is described in Lovd as [Likely_pathogenic].
Transcripts
RefSeq
| Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|
| MLH1 | NM_000249.4 | c.350C>T | p.Thr117Met | missense_variant | 4/19 | ENST00000231790.8 | NP_000240.1 |
Ensembl
| Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Protein | Appris | UniProt |
|---|---|---|---|---|---|---|---|---|---|---|
| MLH1 | ENST00000231790.8 | c.350C>T | p.Thr117Met | missense_variant | 4/19 | 1 | NM_000249.4 | ENSP00000231790 | P1 |
Frequencies
GnomAD3 genomes
GnomAD3 genomes
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33
GnomAD3 exomes AF: 0.00000398 AC: 1AN: 251388Hom.: 0 AF XY: 0.00000736 AC XY: 1AN XY: 135858
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GnomAD4 exome AF: 0.00000821 AC: 12AN: 1461766Hom.: 0 Cov.: 30 AF XY: 0.00000963 AC XY: 7AN XY: 727186
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ClinVar
Significance: Pathogenic
Submissions summary: Pathogenic:29
Revision: reviewed by expert panel
LINK: link
Submissions by phenotype
not provided Pathogenic:11
| Pathogenic, no assertion criteria provided | clinical testing | Mayo Clinic Laboratories, Mayo Clinic | - | - - |
| Pathogenic, criteria provided, single submitter | clinical testing | Clinical Genetics and Genomics, Karolinska University Hospital | Apr 13, 2017 | - - |
| Pathogenic, criteria provided, single submitter | clinical testing | GeneDx | Oct 21, 2021 | Published functional studies demonstrate a damaging effect: abrogated or significantly reduced MMR activity, no dominant mutator effect (Shimodaira 1998, Shcherbakova 1999, Trojan 2002, Plotz 2006, Vogelsang 2009, Hinrichsen 2013, Thompson 2014); Not observed at a significant frequency in large population cohorts (Lek 2016); In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; This variant is associated with the following publications: (PMID: 22736432, 11429708, 23403630, 12377806, 22949379, 25420488, 25980754, 28874130, 10082584, 18547406, 23760103, 22949387, 25117503, 15340264, 19267393, 12200596, 12112654, 14564042, 12373605, 12919140, 11601928, 16395668, 19072991, 15996210, 18726168, 18772310, 21387278, 12555990, 18618713., 21642682, 16995940, 18561205, 17192056, 18383312, 11385712, 11139242, 16451135, 12362047, 16528606, 18566915, 17713103, 15713769, 20215533, 24362816, 9697702, 11781295, 12810663, 17135187, 17510385, 17594722, 19863800, 20864636, 20176959, 20020535, 22753075, 8574961, 27064304, 27601186, 27013479, 22322191, 28127413, 28449805, 28251689, 26681312, 28640387, 25248401, 29478780, 29752822, 28135145, 29505604, 8566964, 10732761, 16830052, 17026620, 9806477, 30521064, 29887214, 30720243, 30998989, 31054147, 31350202, 31491536, 31447099, 31948886, 32719484, 31332305, 33654310) - |
| Pathogenic, criteria provided, single submitter | clinical testing | Revvity Omics, Revvity | Sep 27, 2022 | - - |
| Pathogenic, no assertion criteria provided | clinical testing | Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center | - | - - |
| Pathogenic, no assertion criteria provided | clinical testing | Clinical Genetics, Academic Medical Center | - | - - |
| Pathogenic, no assertion criteria provided | clinical testing | Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ | - | - - |
| Pathogenic, criteria provided, single submitter | clinical testing | Clinical Genetics Laboratory, Skane University Hospital Lund | Dec 01, 2022 | - - |
| Pathogenic, criteria provided, single submitter | clinical testing | Genetic Services Laboratory, University of Chicago | Apr 05, 2021 | - - |
| Pathogenic, criteria provided, single submitter | clinical testing | Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital | Jul 31, 2024 | - - |
| Pathogenic, criteria provided, single submitter | clinical testing | Quest Diagnostics Nichols Institute San Juan Capistrano | Sep 12, 2019 | The MLH1 c.350C>T (p.Thr117Met) variant has been reported in the published literature in individuals affected with a Lynch syndrome associated cancer (PMIDs: 16451135 (2006), 28135145 (2017), 28449805 (2017), 28874130 (2017), 30521064 (2019)). Functional studies show that this variant shows significantly reduced MLH1 protein expression and DNA mismatch repair activity (PMIDs: 11781295 (2002), 17135187 (2006), 17510385 (2007), 23403630 (2013)). The frequency of this variant in the general population, 0.000004 (1/251388 chromosomes (Genome Aggregation Database, http://gnomad.broadinstitute.org)), is consistent with pathogenicity. Based on the available information, this variant is classified as pathogenic. - |
Lynch syndrome Pathogenic:5
| Pathogenic, criteria provided, single submitter | clinical testing | University of Washington Department of Laboratory Medicine, University of Washington | Nov 20, 2015 | - - |
| Pathogenic, reviewed by expert panel | research | International Society for Gastrointestinal Hereditary Tumours (InSiGHT) | Sep 05, 2013 | Abrogated function, >2 MSI-H tumours, co-segregation with disease & MAF 0.00. Multifactorial likelihood analysis posterior probability >0.99 - |
| Pathogenic, criteria provided, single submitter | clinical testing | Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine | Mar 23, 2016 | The p.Thr117Met variant in MLH1 has been reported in >50 individuals with MLH1-a ssociated tumors (Kurzawski 2002, Wei 2003, Liu 1996, Maliaka 1996, Yap 2008, Ca sey 2005; InSiGHT database: http://chromium.lovd.nl/LOVD2/colon_cancer/variants. php) and segregated with disease in at least 2 affected family members (Zavodna 2006). This variant was absent from large population studies. In vitro functiona l studies provide some evidence that the p.Thr117Met variant is deficient in mis match repair (Trojan 2002). Computational prediction tools and conservation anal ysis suggest that this variant may impact the protein, though this information a lone is not predictive enough to determine pathogenicity. Additionally, this var iant has been classified as pathogenic on Nov 26, 2014 by the ClinGen-approved I nSiGHT panel (ClinVar SCV000211908.2). In summary, this variant meets our criter ia to be classified as pathogenic for Lynch syndrome in an autosomal dominant ma nner. ACMG/AMP criteria applied: PS4, PM2, PS3, PP3 (Richards 2015). - |
| Pathogenic, criteria provided, single submitter | clinical testing | Women's Health and Genetics/Laboratory Corporation of America, LabCorp | Apr 15, 2016 | Variant summary: The c.350C>T variant in MLH1 gene is a missense change that alters a highly conserved nucleotide and 4/4 in silico tools predict deleterious outcome. The variant has been reported in multiple affected individuals and was shown to segregate with the disease (Wei_CG_2003). IHC showed selective loss of the MLH1 protein in tumors from patients testing positive for the variant of interest and cells containing the T117M lost the ability to repair mismatched DNA both in vivo and in vitro (Takanashi, 2007; Hinrichsen, 2016). The variant is absent from the large control population dataset of ExAC. Lastly, a reputable database/diagnostic center classified the variant of interest as Pathogenic. Taken together, the variant was classified as Pathogenic. - |
| Pathogenic, criteria provided, single submitter | clinical testing | All of Us Research Program, National Institutes of Health | Oct 30, 2023 | This missense variant replaces threonine with methionine at codon 117 of the MLH1 protein. Computational prediction suggests that this variant may have deleterious impact on protein structure and function (internally defined REVEL score threshold >= 0.7, PMID: 27666373). Multiple functional studies have reported that this variant impacted in vitro mismatch repair activity (PMID: 11781295, 17135187, 17510385, 20020535, 23403630). This variant has been reported in over 20 individuals and families affected with Lynch syndrome (PMID: 8566964, 8574961, 9806477, 10349986, 10480359, 10732761, 11385712, 12362047, 12200596, 12373605, 12919140, 20233461, 15713769, 17026620, 18566915, 19419416, 19698169, 21404117, 22322191, 23403630) and has been reported to segregate with disease in multiple families (PMID: 22949379). This variant has been identified in 1/251388 chromosomes in the general population by the Genome Aggregation Database (gnomAD). Loss of MLH1 function is a known mechanism of disease. Based on the available evidence, this variant is classified as Pathogenic. - |
Colorectal cancer, hereditary nonpolyposis, type 2 Pathogenic:3
| Pathogenic, no assertion criteria provided | literature only | OMIM | Sep 01, 2003 | - - |
| Pathogenic, criteria provided, single submitter | clinical testing | Baylor Genetics | Jan 22, 2024 | - - |
| Pathogenic, criteria provided, single submitter | clinical testing | KCCC/NGS Laboratory, Kuwait Cancer Control Center | Jul 07, 2023 | This sequence change replaces threonine with methionine at codon 117 of the MLH1 protein (p.Thr117Met). This variant is not present in population databases (gnomAD). This variant has been observed in many families and individuals with colon cancer and Lynch syndrome (PMID: 18566915, 22322191, 20233461, 15713769, 12112654, 19698169). ClinVar contains an entry for this variant (Variation ID: 17094). Multiple experimental studies have shown that this missense change results in an unstable protein with disrupted protein interactions and defective mismatch repair activity (PMID: 11781295, 17135187, 23403630, 12810663, 11429708, 17510385, 9697702). A multifactorial likelihood analysis incorporating genetic, clinical, and bioinformatic data (PMID: 19267393), and an algorithm developed specifically for the MLH1 gene (PMID: 18383312), indicate that this variant has a high probability of being pathogenic. In addition, multiple missense mutations have been reported in this region in individuals with colorectal cancer, suggesting that this is an important domain for MLH1 function (PMID: 17510385). In-silico predictions show pathogenic computational verdict based on 11 pathogenic predictions from BayesDel_addAF, DANN, DEOGEN2, EIGEN, FATHMM-MKL, LIST-S2, M-CAP, MVP, MutationAssessor, MutationTaster and SIFT vs 1 benign prediction from PrimateAI and the threonine residue is highly conserved. Therefore, this sequence change has been classified as Pathogenic. - |
Lynch syndrome 1 Pathogenic:2
| Pathogenic, no assertion criteria provided | clinical testing | Pathway Genomics | Jul 24, 2014 | - - |
| Likely pathogenic, no assertion criteria provided | clinical testing | Ding PR Lab, Sun Yat-sen University Cancer Center | - | - - |
Hereditary cancer-predisposing syndrome Pathogenic:2
| Pathogenic, criteria provided, single submitter | clinical testing | Color Diagnostics, LLC DBA Color Health | Apr 07, 2023 | This missense variant replaces threonine with methionine at codon 117 of the MLH1 protein. Computational prediction suggests that this variant may have deleterious impact on protein structure and function (internally defined REVEL score threshold >= 0.7, PMID: 27666373). Multiple functional studies have reported that this variant impacted in vitro mismatch repair activity (PMID: 11781295, 17135187, 17510385, 20020535, 23403630). This variant has been reported in over 20 individuals and families affected with Lynch syndrome (PMID: 8566964, 8574961, 9806477, 10349986, 10480359, 10732761, 11385712, 12362047, 12200596, 12373605, 12919140, 20233461, 15713769, 17026620, 18566915, 19419416, 19698169, 21404117, 22322191, 23403630) and has been reported to segregate with disease in multiple families (PMID: 22949379). This variant has been identified in 1/251388 chromosomes in the general population by the Genome Aggregation Database (gnomAD). Loss of MLH1 function is a known mechanism of disease. Based on the available evidence, this variant is classified as Pathogenic. - |
| Pathogenic, criteria provided, single submitter | clinical testing | Ambry Genetics | Jan 21, 2022 | The p.T117M pathogenic mutation (also known as c.350C>T), located in coding exon 4 of the MLH1 gene, results from a C to T substitution at nucleotide position 350. The threonine at codon 117 is replaced by methionine, an amino acid with similar properties. This mutation has been reported in multiple hereditary non-polyposis colorectal cancer (HNPCC)/Lynch syndrome patients meeting Amsterdam diagnostic criteria; several whose tumors demonstrated high microsatellite instability and/or loss of MLH1 staining by immunohistochemistry (IHC) (Buerstedde JM et al. J. Med. Genet., 1995 Nov;32:909-12; Maliaka YK et al. Hum. Genet., 1996 Feb;97:251-5; Bennett G et al. Clin. Chem. Lab. Med.,1998 Aug;36:641-4; Kurzawski G et al. J Med Genet, 2002 Oct;39:E65; Wei SC et al. Clin Genet, 2003 Sep;64:243-51; Pigatto F et al. Hered Cancer Clin Pract, 2004 Nov;2:175-84; Christensen LL et al. BMC Med Genet, 2008 Jun;9:52; Ollila S et al. Int J Cancer, 2008 Aug;123:720-4; Nilbert M et al. Fam Cancer, 2009 Jun;8:75-83; Choi YH et al. Hered Cancer Clin Pract, 2009 Aug;7:14; Yap HL et al. Fam Cancer, 2009 Aug;8:85-94; Vogelsang M et al. BMC Cancer, 2009 Oct;9:382; Walsh MD et al. Mod Pathol, 2012 May;25:722-30; Toon CW et al. Am J Surg Pathol, 2013 Oct;37:1592-602; Rosty C et al. Fam Cancer, 2014 Dec;13:573-82; Shirts BH et al. Genet Med, 2016 10;18:974-81; Susswein LR et al. Genet Med, 2016 08;18:823-32; Sunga AY et al. Cancer Genet, 2017 04;212-213:1-7; Jiang W et al. Int J Cancer, 2019 05;144:2161-2168; Tian W et al. Int J Cancer, 2019 09;145:1290-1298; Ow SGW et al. Clin Colorectal Cancer, 2019 12;18:e324-e334; Yanus GA et al. Eur J Med Genet, 2020 Mar;63:103753; Talbot A et al. BMC Cancer, 2021 May;21:617; Frostberg E et al. Cancers (Basel), 2021 Oct;13). This mutation has also been reported in breast and prostate cancer cohorts (Walsh MD et al. Clin Cancer Res 2010 Apr;16(7):2214-24; Rosty C et al. Fam Cancer, 2014 Dec;13:573-82; Li JY et al. Int J Cancer, 2019 01;144:281-289; Wu Y et al. Eur Urol Oncol, 2020 04;3:224-230). Multiple functional studies have demonstrated that the T117M alteration has reduced protein expression, deficient MMR activity, inactivated hMLH1-induced dominant mutator effect, and impaired interaction with hPMS2 (Shimodaira H et al. Nat Genet, 1998 Aug;19:384-9; Jäger AC et al. Oncogene, 2001 Jun;20:3590-5; Trojan J et al. Gastroenterology, 2002 Jan;122:211-9; Brieger A et al. Gut, 2002 Nov;51:677-84; Takahashi M et al. Cancer Res, 2007 May;67:4595-604; Drost M et al. Hum Mutat, 2010 Mar;31:247-53; Hinrichsen I et al. Clin Cancer Res, 2013 May;19:2432-41). Two other alterations at the same codon, p.T117R and p.T117K, have been detected in multiple hereditary non-polyposis colorectal cancer (HNPCC)/Lynch syndrome patients meeting Amsterdam diagnostic criteria (Buerstedde JM et al. J. Med. Genet. 1995 Nov;32:909-12; Heinimann K et al Cancer. 1999 Jun 15;85(12):2512-8; Ellison AR et al. Hum Mol Genet. 2001 Sep;10:1889-900; Casey G et al. JAMA. 2005 Feb;293:799-809; Stojcev Z et al. Acta Biochim Pol. 2013 Jun;60:195-8), and based on an internal structural assessment, both of these variants are anticipated to result in a significant decrease in structural stability (Ambry internal data). This alteration has been classified as pathogenic using the following lines of evidence: in silico prediction models, segregation with disease, clinical phenotype including tumor characteristics, mutation co-occurrence, and functional studies (Thompson B et al. Hum Mutat. 2013 Jan;34(1):200-9; Thompson B et al. Nat Genet. 2014 Feb;46(2):107-15; available at [www.insight-group.org/variants/classifications/]). This amino acid position is highly conserved in available vertebrate species. In addition, this alteration is predicted to be deleterious by in silico analysis. Based on the supporting evidence, this alteration is interpreted as a disease-causing mutation. - |
Endometrial carcinoma Pathogenic:2
| Pathogenic, no assertion criteria provided | clinical testing | CZECANCA consortium | Feb 21, 2023 | - - |
| Pathogenic, no assertion criteria provided | clinical testing | Department of Pathology and Laboratory Medicine, Sinai Health System | - | The MLH1 p.Thr117Met variant was identified in the literature in at least 2 of 160 proband chromosomes from Lynch syndrome families, and has been characterized in several functional studies (Andersen 2012, Brieger 2002, Hinrichsen 2013, Jager 2001, Liu 1996, Perera 2010, Plotz 2006, Takahashi 2007, Trojan 2002, Vogelsang 2009), and was previously identified by our laboratory in 1 individual with colorectal cancer. The p.Thr117Met variant was also identified in dbSNP (ID: rs63750781) “With allele of Uncertain significance”, MutDB, HGMD, “Mismatch Repair Genes Variant Database”, “InSiGHT Colon Cancer Database”, “Zhejiang Colon Cancer Database”, “MMR Gene Unclassified Variants Database”, UMD (28X as a Causal variant), LOVD and was classified as pathogenic by InSiGHT and OMIM (submitted within the ClinVar database). The p.Thr117Met residue is conserved across mammals and lower organisms, and computational analyses (PolyPhen-2, SIFT, AlignGVGD, BLOSUM, MutationTaster) suggest that the p.Thr117Met variant may impact the protein. A study by Perera (2010) found that the p.Thr117Met variant was associated with significantly unbalanced allelic expression, and tumour analysis of the positive proband showed MLH1-deficiency and high microsatellite instability, suggesting that this could be considered a deleterious mutation. Functional studies characterizing the variant demonstrated reduced mismatch repair activity and nuclear localization (Andersen_2012, Brieger 2002, Jager 2001, Trojan 2002, Takahashi 2007, Plotz 2006, Vogelsang 2009); some of these studies detected normal expression of MLH1 and interaction with PMS2, while other studies found a reduction in MLH1 expression and PMS2 interaction. Three studies have suggested that the p.Thr117Met missense mutation may inactivate mismatch repair (MMR) activity by altering the capacity of this mutant protein to bind and/or hydrolyze adenosine triphosphate (ATP) (Brieger 2002, Jager 2001, Drost 2009). In summary, based on the above information, this variant meets our laboratory’s criteria to be classified as pathogenic. - |
Inherited MMR deficiency (Lynch syndrome) Pathogenic:1
| Pathogenic, criteria provided, single submitter | clinical testing | Genomics and Molecular Medicine Service, East Genomic Laboratory Hub, NHS Genomic Medicine Service | Apr 24, 2024 | PS4_Very Strong,PM2,PP3,PP4_Very Strong - |
Lynch-like syndrome Pathogenic:1
| Pathogenic, no assertion criteria provided | clinical testing | Constitutional Genetics Lab, Leon Berard Cancer Center | Jul 01, 2019 | - - |
Hereditary nonpolyposis colorectal neoplasms Pathogenic:1
| Pathogenic, criteria provided, single submitter | clinical testing | Labcorp Genetics (formerly Invitae), Labcorp | Nov 27, 2023 | This sequence change replaces threonine, which is neutral and polar, with methionine, which is neutral and non-polar, at codon 117 of the MLH1 protein (p.Thr117Met). This variant is present in population databases (rs63750781, gnomAD 0.003%). This missense change has been observed in individual(s) with colon cancer and Lynch syndrome (PMID: 12112654, 15713769, 18566915, 19698169, 20233461, 22322191). ClinVar contains an entry for this variant (Variation ID: 17094). Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is expected to disrupt MLH1 protein function with a positive predictive value of 95%. Experimental studies have shown that this missense change affects MLH1 function (PMID: 9697702, 11429708, 11781295, 12810663, 17135187, 17510385, 23403630). This variant disrupts the p.Thr117 amino acid residue in MLH1. Other variant(s) that disrupt this residue have been determined to be pathogenic (PMID: 9697702, 11555625, 12810663). This suggests that this residue is clinically significant, and that variants that disrupt this residue are likely to be disease-causing. For these reasons, this variant has been classified as Pathogenic. - |
Colon cancer Pathogenic:1
| Pathogenic, criteria provided, single submitter | clinical testing | KCCC/NGS Laboratory, Kuwait Cancer Control Center | May 31, 2023 | is neutral and non-polar, at codon 117 of the MLH1 protein (p.Thrl 17Met). This variant is present in population databases (rs63750781, gnomAD 0.003%). This missense change has been observed in individual(s) with colon cancer and Lynch syndrome (PMID: 12112654, 15713769, 18566915, 19698169, 20233461, 22322191). ClinVar contains an entry for this variant (Variation ID: 17094). Experimental studies have shown that this missense change affects MLH1 function (PMID: 9697702, 11429708, 1178i295, 12810663, 17135187, 17510385, 23403630). This variant disrupts the p.Thrl 17 amino acid residue in MLH1. Other variant(s) that disrupt this residue have been determined to be pathogenic (PMID: 9697702, 11555625, 12810663). This suggests that this residue is clinically significant, and that variants that disrupt this residue are likely to be disease-causing. For these reasons, this variant has been classified as Pathogenic. Pathogenic/likely pathogenic variants in the MLH1 gene are known to cause Hereditary Non-Polyposis Colorectal Cancer Syndrome, also known as Lynch Syndrome. - |
Computational scores
Source:
Name
Calibrated prediction
Score
Prediction
AlphaMissense
Pathogenic
BayesDel_addAF
Pathogenic
D
BayesDel_noAF
Pathogenic
CADD
Pathogenic
DANN
Pathogenic
DEOGEN2
Pathogenic
D;.;D
Eigen
Pathogenic
Eigen_PC
Pathogenic
FATHMM_MKL
Pathogenic
D
LIST_S2
Pathogenic
D;D;D
M_CAP
Pathogenic
D
MetaRNN
Pathogenic
D;D;D
MetaSVM
Pathogenic
D
MutationAssessor
Pathogenic
H;.;.
MutationTaster
Benign
D;D;D;D;D;D
PrimateAI
Uncertain
T
PROVEAN
Pathogenic
D;D;D
REVEL
Pathogenic
Sift
Pathogenic
D;D;D
Sift4G
Pathogenic
D;D;D
Polyphen
D;.;.
Vest4
MVP
MPC
ClinPred
D
GERP RS
Varity_R
gMVP
Splicing
Name
Calibrated prediction
Score
Prediction
SpliceAI score (max)
Details are displayed if max score is > 0.2
Find out detailed SpliceAI scores and Pangolin per-transcript scores at