NM_001365999.1(SZT2):c.8594C>T (p.Pro2865Leu) AND not provided
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Oct 3, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001201391.11
Allele description [Variation Report for NM_001365999.1(SZT2):c.8594C>T (p.Pro2865Leu)]
NM_001365999.1(SZT2):c.8594C>T (p.Pro2865Leu)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Sequence 7937 from patent US 9572897
Sequence 7937 from patent US 9572897gi|1257107096|gb|ATK68760.1||pat|US 897|7937Protein
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024