NM_001386140.1(MTTP):c.267T>C (p.Val89=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 19, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001428910.6
Allele description [Variation Report for NM_001386140.1(MTTP):c.267T>C (p.Val89=)]
NM_001386140.1(MTTP):c.267T>C (p.Val89=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Rattus norvegicus kelch-like family member 12 (Klhl12), mRNA
Rattus norvegicus kelch-like family member 12 (Klhl12), mRNAgi|402692116|ref|NM_153730.2|Nucleotide
-
LOC130067545 [Homo sapiens]
LOC130067545 [Homo sapiens]Gene ID:130067545Gene
-
LOC130067569 [Homo sapiens]
LOC130067569 [Homo sapiens]Gene ID:130067569Gene
-
LOC110740340 [Homo sapiens]
LOC110740340 [Homo sapiens]Gene ID:110740340Gene
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024