NM_000038.6(APC):c.532-32T>C AND not provided
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Dec 26, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000833671.14
Allele description [Variation Report for NM_000038.6(APC):c.532-32T>C]
NM_000038.6(APC):c.532-32T>C
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
PREDICTED: Homo sapiens mutL homolog 3 (MLH3), transcript variant X14, mRNA
PREDICTED: Homo sapiens mutL homolog 3 (MLH3), transcript variant X14, mRNAgi|2217297156|ref|XM_047431268.1|Nucleotide
-
262190 (1)
OMIM
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Last Updated: Oct 13, 2024