NM_001126049.2(KLLN):c.-792C>T AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 14, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002477276.8
Allele description [Variation Report for NM_001126049.2(KLLN):c.-792C>T]
NM_001126049.2(KLLN):c.-792C>T
Condition(s)
- Name:
- Macrocephaly-autism syndrome
- Synonyms:
- Macrocephaly/autism syndrome
- Identifiers:
- MONDO: MONDO:0011537; MedGen: C1854416; Orphanet: 210548; OMIM: 605309
- Name:
- Familial meningioma
- Synonyms:
- Meningioma, familial, susceptibility to
- Identifiers:
- MONDO: MONDO:0011789; MedGen: C3551915; Orphanet: 263662; OMIM: 607174
- Name:
- Malignant tumor of prostate
- Synonyms:
- Prostate cancer
- Identifiers:
- MONDO: MONDO:0008315; MedGen: C0376358; Orphanet: 1331; Human Phenotype Ontology: HP:0012125
-
Fundulus lineolatus voucher NAFF 3097 cytochrome oxidase subunit 1 (COI) gene, p...
Fundulus lineolatus voucher NAFF 3097 cytochrome oxidase subunit 1 (COI) gene, partial cds; mitochondrialgi|339769619|gnl|uoguelph|BNAFA482- I-5P|gb|JN026658.1|Nucleotide
-
HADHB [Panthera tigris]
HADHB [Panthera tigris]Gene ID:102966174Gene
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Last Updated: Aug 25, 2024