NM_018139.3(DNAAF2):c.1299C>T (p.Pro433=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000254371.5
Allele description [Variation Report for NM_018139.3(DNAAF2):c.1299C>T (p.Pro433=)]
NM_018139.3(DNAAF2):c.1299C>T (p.Pro433=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
SORBS2 sorbin and SH3 domain containing 2 [Homo sapiens]
SORBS2 sorbin and SH3 domain containing 2 [Homo sapiens]Gene ID:8470Gene
-
Gene Links for GEO Profiles (Select 35877586) (1)
Gene
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Last Updated: Mar 10, 2024