Variant
MLH1 Glu34Lys (c.100G>A)
CI-VAR-00001863Explore in graph →NM_000249.3:c.100G>ACIViC 2346
Curated evidence
Evidence by cancer (1 items)
Grouped by cancer context first, then therapy. The same variant can be sensitizing in one cancer and irrelevant in another — contexts are never merged. 50 items per page; a cancer group may continue on the next page.
civicProvenance
- Source
- CIViC — Clinical Interpretation of Variants in Cancer
- Dataset
- CIViC evidence items
- Version
- civic-2026-09-08
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- expert curation
- License
- CC0 1.0
- PMID
- 29887214
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Lynch Syndrome1unmapped disease | ||||||||
| MLH1 Glu34Lys (c.100G>A) | (diagnostic) | Diagnostic | C | Supports Positive | 3 | submitted | EID6225Somatic mutation with evidence of loss of heterozygosity in an MSI-H tumor. PMID 29887214 · Shirts et al., 2018 · Open in CIViC | civic |
ClinVar
Clinical significance (0)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
Data not yet available
No ClinVar interpretation attached to this variant.