NM_023944.4(CYP4F12):c.253T>C (p.Ser85Pro) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 8, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004194691.1
Allele description [Variation Report for NM_023944.4(CYP4F12):c.253T>C (p.Ser85Pro)]
NM_023944.4(CYP4F12):c.253T>C (p.Ser85Pro)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens tetraspanin 6 (TSPAN6), transcript variant 2, mRNA
Homo sapiens tetraspanin 6 (TSPAN6), transcript variant 2, mRNAgi|1675114476|ref|NM_001278740.2|Nucleotide
-
Hereditary Spastic Paraplegia Overview - GeneReviews®
Hereditary Spastic Paraplegia Overview - GeneReviews®
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See more...Assertion and evidence details
Last Updated: Jul 15, 2024