NM_005228.5(EGFR):c.18G>T (p.Thr6=) AND EGFR-related lung cancer
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 17, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001408821.6
Allele description [Variation Report for NM_005228.5(EGFR):c.18G>T (p.Thr6=)]
NM_005228.5(EGFR):c.18G>T (p.Thr6=)
Condition(s)
- Name:
- EGFR-related lung cancer (EGFR)
- Identifiers:
- MedGen: CN130014
-
Homo sapiens APC, WNT signaling pathway regulator (APC), transcript variant 3, m...
Homo sapiens APC, WNT signaling pathway regulator (APC), transcript variant 3, mRNAgi|307133686|ref|NM_000038.5|Nucleotide
-
Chain H, CarB
Chain H, CarBgi|75766087|pdb|2A7K|HProtein
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Last Updated: Feb 28, 2024