Variant (rsID / SNP)
rs121913247
rs121913247 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MET. Location: chromosome 7, position 116,423,413. Clinical significance in the table: Uncertain significance.
Reference-table entries
METUncertain significance
- Clinical significance (as recorded)
- Uncertain significance
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:116423413
- Cytoband
- 7q31.2
- HGVS
- NM_000245.4(MET):c.3688T>C (p.Tyr1230His)
- Allele change
- Missense_Y800H
Associated conditions / phenotypes
Carcinoma|Renal carcinoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.