Variant (rsID / SNP)
rs1047972
rs1047972 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AURKA. Location: chromosome 20, position 54,961,463. The table records no clinical significance for this variant.
Reference-table entries
AURKANot classified
- Variant type
- missense_variant
- Chromosome / position
- 20:54961463
- HGVS
- NM_001323303.2,c.169A>G,p.Ile57Val
- Allele change
- Missense_I57V
Associated conditions / phenotypes
Gastric Cancer|Lung Cancer Susceptibility 3|Adenocarcinoma|Oral Squamous Cell Carcinoma|Hepatocellular Carcinoma|Oral Cancer|Wilms Tumor 5|Cervical Cancer|Neuroblastoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.