ClinVar
|
Risk
|
rs1057519896(A;A) rs1057519896(T;T) |
Alt
|
rs1057519896(A;A) rs1057519896(T;T) |
Reference
|
Rs1057519896(G;G) |
Significance |
Probable-Pathogenic |
Disease |
Oesophageal carcinoma Squamous cell carcinoma of the head and neck Adenocarcinoma of stomach Uterine cervical neoplasms Ovarian Serous Cystadenocarcinoma Uterine Carcinosarcoma Squamous cell carcinoma of lung Transitional cell carcinoma of the bladder Malignant melanoma of skin Colorectal Neoplasms Malignant neoplasm of body of uterus Chronic lymphocytic leukemia |
Variation | info |
---|
Gene |
FBXW7 |
CLNDBN |
Oesophageal carcinoma Squamous cell carcinoma of the head and neck Adenocarcinoma of stomach Uterine cervical neoplasms Ovarian Serous Cystadenocarcinoma Uterine Carcinosarcoma Squamous cell carcinoma of lung Transitional cell carcinoma of the bladder Malignant melanoma of skin Colorectal Neoplasms Malignant neoplasm of body of uterus Chronic lymphocytic leukemia |
Reversed |
1 |
HGVS |
NC_000004.11:g.153247288C>A; NC_000004.11:g.153247288C>T |
CLNSRC |
|
CLNACC |
RCV000418253.1, RCV000420626.1, RCV000421948.1, RCV000423047.1, RCV000428228.1, RCV000428507.1, RCV000429608.1, RCV000433338.1, RCV000434990.1, RCV000438226.1, RCV000439579.1, RCV000439833.1, RCV000418430.1, RCV000423701.1, RCV000424983.1, RCV000425614.1, RCV000427831.1, RCV000431557.1, RCV000434393.1, RCV000435656.1, RCV000436317.1, RCV000440517.1, RCV000442928.1, RCV000443929.1, |