ClinVar
|
Risk
|
rs121913255(C;C) rs121913255(T;T) |
Alt
|
rs121913255(C;C) rs121913255(T;T) |
Reference
|
Rs121913255(A;A) |
Significance |
Pathogenic |
Disease |
not provided Glioblastoma Acute myeloid leukemia Hepatocellular carcinoma Neoplasm of the thyroid gland Nasopharyngeal Neoplasms Multiple myeloma Adrenocortical carcinoma Malignant melanoma of skin Ovarian Serous Cystadenocarcinoma Chronic lymphocytic leukemia Malignant neoplasm of body of uterus Transitional cell carcinoma of the bladder Adenocarcinoma of stomach Colorectal Neoplasms Malignant melanoma Renal cell carcinoma Adenocarcinoma of lung Neoplasm of brain Non-small cell lung cancer |
Variation | info |
---|
Gene |
NRAS |
CLNDBN |
not provided Glioblastoma Acute myeloid leukemia Hepatocellular carcinoma Neoplasm of the thyroid gland Nasopharyngeal Neoplasms Multiple myeloma Adrenocortical carcinoma Malignant melanoma of skin Ovarian Serous Cystadenocarcinoma Chronic lymphocytic leukemia Malignant neoplasm of body of uterus Transitional cell carcinoma of the bladder Adenocarcinoma of stomach Colorectal Neoplasms Malignant melanoma Renal cell carcinoma Adenocarcinoma of lung Neoplasm of brain Non-small cell lung cancer |
Reversed |
1 |
HGVS |
NC_000001.10:g.115256528T>A; NC_000001.10:g.115256528T>G |
CLNSRC |
|
CLNACC |
RCV000414646.1, RCV000418758.1, RCV000419887.1, RCV000420139.1, RCV000420910.1, RCV000422093.1, RCV000424220.1, RCV000427364.1, RCV000428418.1, RCV000429512.1, RCV000429704.1, RCV000431603.1, RCV000434043.1, RCV000436881.1, RCV000437158.1, RCV000438233.1, RCV000439006.1, RCV000439308.1, RCV000444600.1, RCV000426637.1, RCV000436751.1, RCV000443672.1, |