NM_001350562.2(TJAP1):c.1115C>T (p.Pro372Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 28, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004233668.1
Allele description [Variation Report for NM_001350562.2(TJAP1):c.1115C>T (p.Pro372Leu)]
NM_001350562.2(TJAP1):c.1115C>T (p.Pro372Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
LOC121825243 [Peromyscus maniculatus bairdii]
LOC121825243 [Peromyscus maniculatus bairdii]Gene ID:121825243Gene
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024