Variant (rsID / SNP)
rs121913238
rs121913238 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRAS. Location: chromosome 12, position 25,380,277. Clinical significance in the table: Pathogenic.
Reference-table entries
KRASPathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:25380277
- Cytoband
- 12p12.1
- HGVS
- NM_004985.5(KRAS):c.181C>A (p.Gln61Lys)
- Allele change
- Missense_Q61E
Associated conditions / phenotypes
Non-small cell lung carcinoma|Thyroid tumor|Neoplasm of the large intestine
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.