Variant (rsID / SNP)
rs17851045
rs17851045 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRAS. Location: chromosome 12, position 25,380,275. Clinical significance in the table: Pathogenic/Likely pathogenic.
Reference-table entries
- Clinical significance (as recorded)
- Pathogenic/Likely pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:25380275
- Cytoband
- 12p12.1
- HGVS
- NM_004985.5(KRAS):c.183A>T (p.Gln61His)
- Allele change
- Missense_Q61H
Associated conditions / phenotypes
Non-small cell lung carcinoma|Neoplasm of the large intestine|Malignant melanoma of skin|Thyroid tumor|Hepatocellular carcinoma|Squamous cell lung carcinoma|Multiple myeloma|Lung adenocarcinoma|Acute myeloid leukemia|B-cell chronic lymphocytic leukemia|Malignant neoplasm of body of uterus|Transitional cell carcinoma of the bladder|Pancreatic adenocarcinoma|Gastric adenocarcinoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.