NM_000137.4(FAH):c.607-18A>G AND Tyrosinemia type I
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 27, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003634230.2
Allele description [Variation Report for NM_000137.4(FAH):c.607-18A>G]
NM_000137.4(FAH):c.607-18A>G
Condition(s)
- Name:
- Tyrosinemia type I (TYRSN1)
- Synonyms:
- Tyrosinemia type 1; Hepatorenal tyrosinemia; FAH deficiency; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0010161; MedGen: C0268490; Orphanet: 882; OMIM: 276700
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lysine-specific histone demethylase 1 [Populus alba x Populus x berolinensis]
lysine-specific histone demethylase 1 [Populus alba x Populus x berolinensis]gi|2459720836|gb|KAJ7005695.1||gnl| AQIZT|cds.Poabs.A02G000232.1.v1.0Protein
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Profile neighbors for GEO Profiles (Select 32366558) (200)
GEO Profiles
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BioProject Links for Protein (Select 1970426538) (1)
BioProject
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BioProject Links for Protein (Select 1970426540) (1)
BioProject
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024