NM_001126049.2(KLLN):c.-898G>A AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 18, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000115555.6
Allele description [Variation Report for NM_001126049.2(KLLN):c.-898G>A]
NM_001126049.2(KLLN):c.-898G>A
Condition(s)
- Name:
- Hereditary cancer-predisposing syndrome
- Synonyms:
- Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672
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Homo sapiens tyrosine kinase with immunoglobulin-like and EGF-like domains 1 (TI...
Homo sapiens tyrosine kinase with immunoglobulin-like and EGF-like domains 1 (TIE1), mRNAgi|31543809|ref|NM_005424.2|Nucleotide
-
Homo sapiens ATPase, H+ transporting, lysosomal V0 subunit a2, mRNA (cDNA clone ...
Homo sapiens ATPase, H+ transporting, lysosomal V0 subunit a2, mRNA (cDNA clone MGC:87365 IMAGE:30344468), complete cdsgi|46250258|gb|BC068531.1|Nucleotide
-
FDFT1 [Ficedula albicollis]
FDFT1 [Ficedula albicollis]Gene ID:101815980Gene
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Last Updated: Oct 20, 2024