NM_001319217.2(CYP1A1):c.1532G>T (p.Arg511Leu) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jun 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000971306.3
Allele description [Variation Report for NM_001319217.2(CYP1A1):c.1532G>T (p.Arg511Leu)]
NM_001319217.2(CYP1A1):c.1532G>T (p.Arg511Leu)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Fam89b family with sequence similarity 89, member B [Mus musculus]
Fam89b family with sequence similarity 89, member B [Mus musculus]Gene ID:17826Gene
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Dec 24, 2023