NM_000255.4(MMUT):c.1515T>C (p.Ile505=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 11, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000601351.1
Allele description [Variation Report for NM_000255.4(MMUT):c.1515T>C (p.Ile505=)]
NM_000255.4(MMUT):c.1515T>C (p.Ile505=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
FGA protein [Homo sapiens]
FGA protein [Homo sapiens]gi|18088463|gb|AAH20764.1|Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Oct 8, 2024