NM_153676.4(USH1C):c.1874C>T (p.Ala625Val) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 24, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000156677.4
Allele description [Variation Report for NM_153676.4(USH1C):c.1874C>T (p.Ala625Val)]
NM_153676.4(USH1C):c.1874C>T (p.Ala625Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens F-box and leucine rich repeat protein 2 (FBXL2), transcript variant...
Homo sapiens F-box and leucine rich repeat protein 2 (FBXL2), transcript variant 1, mRNAgi|284447307|ref|NM_012157.3|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Dec 24, 2022