NM_001953.5(TYMP):c.1242G>A (p.Pro414=) AND Mitochondrial neurogastrointestinal encephalomyopathy
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 9, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001272323.9
Allele description [Variation Report for NM_001953.5(TYMP):c.1242G>A (p.Pro414=)]
NM_001953.5(TYMP):c.1242G>A (p.Pro414=)
Condition(s)
-
K-EST0144908 S14K402 Homo sapiens cDNA clone S14K402-59-H06 5', mRNA sequence
K-EST0144908 S14K402 Homo sapiens cDNA clone S14K402-59-H06 5', mRNA sequencegi|19941156|gnl|dbEST|11986804|gb|B 87.1|Nucleotide
-
Uterine cancer
Uterine cancerMedGen
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See more...Assertion and evidence details
Last Updated: Sep 16, 2024