ClinVar
|
Risk
|
rs121913237(A;A) rs121913237(C;C) rs121913237(T;T) |
Alt
|
rs121913237(A;A) rs121913237(C;C) rs121913237(T;T) |
Reference
|
Rs121913237(G;G) |
Significance |
Pathogenic |
Disease |
Noonan syndrome not provided Malignant melanoma Multiple myeloma Adenocarcinoma of stomach Acute myeloid leukemia Myelodysplastic syndrome Malignant melanoma of skin Malignant neoplasm of body of uterus Colorectal Neoplasms Myelodysplastic syndrome progressed to acute myeloid leukemia Non-small cell lung cancer Epidermal nevus Juvenile myelomonocytic leukemia |
Variation | info |
---|
Gene |
NRAS |
CLNDBN |
Noonan syndrome not provided Malignant melanoma Multiple myeloma Adenocarcinoma of stomach Acute myeloid leukemia Myelodysplastic syndrome Malignant melanoma of skin Malignant neoplasm of body of uterus Colorectal Neoplasms Myelodysplastic syndrome progressed to acute myeloid leukemia Non-small cell lung cancer Epidermal nevus Juvenile myelomonocytic leukemia |
Reversed |
1 |
HGVS |
NC_000001.10:g.115258747C>A; NC_000001.10:g.115258747C>G; NC_000001.10:g.115258747C>T |
CLNSRC |
OMIM Allelic Variant UniProtKB (protein) |
CLNACC |
RCV000037576.2, RCV000158986.1, RCV000419124.1, RCV000421072.1, RCV000423890.1, RCV000429393.1, RCV000432178.1, RCV000438750.1, RCV000438967.1, RCV000439421.1, RCV000203450.1, RCV000380895.2, RCV000418647.1, RCV000425963.1, RCV000426950.1, RCV000427550.1, RCV000433455.1, RCV000434113.1, RCV000437165.1, RCV000444591.1, RCV000444670.1, RCV000032849.7, RCV000144963.3, RCV000158980.2, RCV000417702.1, RCV000417869.1, RCV000424239.1, RCV000427949.1, RCV000430706.1, RCV000434517.1, RCV000436228.1, RCV000439064.1, RCV000440963.1, |