About MSH2
No gene-level summary was recorded for this case.
No variant summary was recorded for this case.
Five-step scale from benign to pathogenic. This variant is uncertain. Select a step to read what it means.
Uncertain.The recorded classification is uncertain significance.
Gene-level background from the recorded interpretation.
Words with a dotted underline have a short definition. Hover or tap them.No gene-level summary was recorded for this case.
The recorded framework is ClinGen MSH2 VCEP v2.0.0. The criteria and strengths shown below come from the saved assessment; this page does not recalculate the classification.
The applied criteria and their strengths are shown as assessed under the stated framework.
This variant is absent from gnomAD v4.1 and gnomAD v2.1, so the observed population frequency is below the MSH2 PM2 threshold of <0.00002 (<1 in 50,000 alleles), supporting PM2 at supporting strength.
This variant is a frameshift duplication predicted to cause p.(Ser268PhefsTer16), introducing a premature termination codon at codon 283. Under the MSH2 InSiGHT specification, nonsense or frameshift variants introducing a premature stop codon at or before codon 891 meet PVS1 at very strong strength, and this truncation is well upstream of that threshold.
No benign criterion marked as applied in the recorded assessment.
Applied the explicit InSiGHT/CSPEC final-classification framework from final_classification_framework.json (source: cspec_ruleset; Richards et al. 2015 combining rules as represented in the retrieved CSPEC ruleset), rather than generic ACMG fallback rules.
Evidence summaries and captured source records, where available. Missing entries should not be interpreted as negative findings.
gnomAD v4.1 allele counts were not recorded for this variant.
Absent from gnomAD v2.1.
No SpliceAI or REVEL score is recorded in the fields used for this tile.
A ClinVar laboratory submission summary was not recorded.
OncoKB classifies this variant as Likely Oncogenic; biological effect: Likely Loss-of-function.
No COSMIC evidence statement is recorded in this case.
This variant does not lie in a statistically significant hotspot.
ACMG/AMP criteria under ClinGen MSH2 VCEP v2.0.0, with the data and sources behind each one.
28 criteria with recorded statuses: 2 met · 2 not met · 7 not assessed · 17 not applicable. Open any row for the full reasoning, the rule and the evidence behind it.
The MSH2 c.802dup (p.(Ser268PhefsTer16)) variant has not been observed in somatic cancers in COSMIC and has been reported in ClinVar as pathogenic by 1 clinical laboratory.
This variant is absent from gnomAD v2.1 and gnomAD v4.1, which is below the MSH2 PM2 threshold of <0.00002 (<1 in 50,000 alleles).
The duplication causes a frameshift with a premature stop codon at p.(Ser268PhefsTer16), and this truncation is upstream of the MSH2 codon 891 cutoff for PVS1 Very Strong in the InSiGHT specification.
SpliceAI predicts no significant splice impact with a maximum delta score of 0.06, indicating no additional splice effect is predicted beyond the truncating consequence of the duplication.
No criteria match.
Absent/extremely rare allele frequency <0.00002 (<1 in 50,000 alleles) in gnomAD v4 dataset.
Nonsense/frameshift variant introducing premature termination codon <= codon 891 in MSH2.
GnomAD v4 Grpmax filtering allele frequency >=0.0001 and <0.001, excluding founder pathogenic variants.
GnomAD v4 Grpmax filtering allele frequency >=0.001, excluding founder pathogenic variants.
1 CRC/endometrial MSI-H tumor and/or loss of MMR protein expression consistent with the variant location for supporting strength; stronger levels require additional independent tumors.
Lack of co-segregation with disease in pedigree(s) with a combined Bayes likelihood ratio <0.05 for strong or >0.05 and <=0.48 for supporting.
De novo points-based framework: >=4 very strong, 2-3.5 strong, 1-1.5 moderate, 0.5 supporting.
Co-segregation with disease in pedigree(s) with a combined Bayes likelihood ratio >2.08 to <=4.3 for supporting, >4.3 to <=18.7 for moderate, and >18.7 in >=2 families for strong.
Mismatch-repair-inconsistent tumor evidence framework for supporting or strong benign evidence.
Co-occurrence in trans with a known pathogenic sequence variant in a patient whose phenotype argues against CMMRD.
Points-based in trans framework: 0.5 supporting, 1-1.5 moderate, 2-3.5 strong, >=4 very strong.
Every interpreted variant in MSH2, mapped onto the exon structure of NM_000251.3. Select a row to find it on the plot.
| Protein | Location | Classification | Link |
|---|
Absent from gnomAD v4.1.
Absent from gnomAD v2.1.
SpliceAI predicts no significant splice impact for this variant (max delta score = 0.06).
0 paper records listed. No publication is explicitly linked to an applied criterion in the recorded metadata.
Screenshots represent source records captured during evidence collection. Select one to view the recorded source content.
The evidence statements recorded by the interpretation pipeline. They have not been reinterpreted by the page.
Absent from gnomAD v4.1.
Absent from gnomAD v2.1.
This variant has been reported in ClinVar as Pathogenic (1 clinical laboratory).
SpliceAI predicts no significant splice impact for this variant (max delta score = 0.06).
OncoKB classifies this variant as Likely Oncogenic; biological effect: Likely Loss-of-function.
This variant does not lie in a statistically significant hotspot. This variant has not previously been reported in somatic cancers (COSMIC).
This variant does not lie in a statistically significant hotspot.