ClinVar
|
Risk
|
rs1057519932(G;G) |
Alt
|
rs1057519932(G;G) |
Reference
|
Rs1057519932(T;T) |
Significance |
Probable-Pathogenic |
Disease |
Brainstem glioma Medulloblastoma Renal cell carcinoma Malignant neoplasm of body of uterus Squamous cell carcinoma of the head and neck Adenocarcinoma of prostate Hepatocellular carcinoma Squamous cell carcinoma of lung Pancreatic adenocarcinoma Ovarian Serous Cystadenocarcinoma Glioblastoma Malignant melanoma of skin Neoplasm of breast Adenocarcinoma of stomach Transitional cell carcinoma of the bladder Uterine cervical neoplasms Oesophageal carcinoma Adenocarcinoma of lung Colorectal Neoplasms Adrenocortical carcinoma Neoplasm of brain Uterine Carcinosarcoma |
Variation | info |
---|
Gene |
PIK3CA |
CLNDBN |
Brainstem glioma Medulloblastoma Renal cell carcinoma Malignant neoplasm of body of uterus Squamous cell carcinoma of the head and neck Adenocarcinoma of prostate Hepatocellular carcinoma Squamous cell carcinoma of lung Pancreatic adenocarcinoma Ovarian Serous Cystadenocarcinoma Glioblastoma Malignant melanoma of skin Neoplasm of breast Adenocarcinoma of stomach Transitional cell carcinoma of the bladder Uterine cervical neoplasms Oesophageal carcinoma Adenocarcinoma of lung Colorectal Neoplasms Adrenocortical carcinoma Neoplasm of brain Uterine Carcinosarcoma |
Reversed |
0 |
HGVS |
NC_000003.11:g.178952086T>G |
CLNSRC |
|
CLNACC |
RCV000418650.1, RCV000418770.1, RCV000419872.1, RCV000423601.1, RCV000423888.1, RCV000425154.1, RCV000425376.1, RCV000427565.1, RCV000429930.1, RCV000430152.1, RCV000431246.1, RCV000431731.1, RCV000433980.1, RCV000434142.1, RCV000435397.1, RCV000436517.1, RCV000436651.1, RCV000440716.1, RCV000441288.1, RCV000441412.1, RCV000442558.1, RCV000443463.1, |