NM_001077446.4(TSEN34):c.542C>A (p.Ser181Tyr) AND not provided
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Jun 2, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000311301.5
Allele description [Variation Report for NM_001077446.4(TSEN34):c.542C>A (p.Ser181Tyr)]
NM_001077446.4(TSEN34):c.542C>A (p.Ser181Tyr)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
txid2286119[Organism:noexp] (1)
Identical Protein Groups
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Dec 24, 2023