NM_144670.6(A2ML1):c.1066C>T (p.Pro356Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004036918.1
Allele description [Variation Report for NM_144670.6(A2ML1):c.1066C>T (p.Pro356Ser)]
NM_144670.6(A2ML1):c.1066C>T (p.Pro356Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Same Parent, Stereochemistry for PubChem Compound (Select 1637288... (2)
Same Parent, Stereochemistry for PubChem Compound (Select 163728815)SearchPubChem Compound
-
Homologene neighbors for GEO Profiles (Select 125183960) (0)
GEO Profiles
-
Profile neighbors for GEO Profiles (Select 125171501) (200)
GEO Profiles
-
Profile neighbors for GEO Profiles (Select 125193285) (200)
GEO Profiles
-
Profile neighbors for GEO Profiles (Select 19351529) (200)
GEO Profiles
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024