NM_001159773.2(CANT1):c.933C>T (p.Asp311=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 29, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003726638.1
Allele description
NM_001159773.2(CANT1):c.933C>T (p.Asp311=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
PREDICTED: Homo sapiens mitochondrial ribosome associated GTPase 2 (MTG2), trans...
PREDICTED: Homo sapiens mitochondrial ribosome associated GTPase 2 (MTG2), transcript variant X4, mRNAgi|2217335019|ref|XM_047440104.1|Nucleotide
-
Homo sapiens mitochondrial ribosome associated GTPase 2 (MTG2), transcript varia...
Homo sapiens mitochondrial ribosome associated GTPase 2 (MTG2), transcript variant 13, non-coding RNAgi|1858589353|ref|NR_169206.1|Nucleotide
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Last Updated: Feb 28, 2024