Variant (rsID / SNP)
rs121913255
rs121913255 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NRAS. Location: chromosome 1, position 115,256,528. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:115256528
- Cytoband
- 1p13.2
- HGVS
- NM_002524.5(NRAS):c.183A>T (p.Gln61His)
- Allele change
- Missense_Q61H
Associated conditions / phenotypes
Glioblastoma|Acute myeloid leukemia|Hepatocellular carcinoma|Thyroid tumor|Nasopharyngeal neoplasm|Multiple myeloma|Adrenal cortex carcinoma|Malignant melanoma of skin|B-cell chronic lymphocytic leukemia|Ovarian serous cystadenocarcinoma|Malignant neoplasm of body of uterus|Transitional cell carcinoma of the bladder|Neoplasm of the large intestine|Gastric adenocarcinoma|Renal cell carcinoma, papillary, 1|Lung adenocarcinoma|Melanoma|Neoplasm of brain|Noonan syndrome and Noonan-related syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.