NM_000141.5(FGFR2):c.*1126T>C AND Isolated coronal synostosis
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000285358.6
Allele description [Variation Report for NM_000141.5(FGFR2):c.*1126T>C]
NM_000141.5(FGFR2):c.*1126T>C
Condition(s)
- Name:
- Isolated coronal synostosis
- Identifiers:
- MedGen: CN043619
-
Homo sapiens BCL2 like 12 (BCL2L12), transcript variant 12, mRNA
Homo sapiens BCL2 like 12 (BCL2L12), transcript variant 12, mRNAgi|2170955310|ref|NM_001282521.2|Nucleotide
-
GEO Profile Links for Gene (Select 9240) (1481)
GEO Profiles
-
txid1506995[Organism:noexp] (174)
Nucleotide
-
coro6 [Anguilla rostrata]
coro6 [Anguilla rostrata]Gene ID:135263425Gene
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See more...Assertion and evidence details
Last Updated: May 12, 2024