ClinVar
|
Risk
|
rs121434596(A;A) rs121434596(C;C) rs121434596(T;T) |
Alt
|
rs121434596(A;A) rs121434596(C;C) rs121434596(T;T) |
Reference
|
Rs121434596(G;G) |
Significance |
Pathogenic |
Disease |
Neoplasm Malignant melanoma Multiple myeloma Malignant melanoma of skin Medulloblastoma Acute myeloid leukemia Adenocarcinoma of stomach Transitional cell carcinoma of the bladder Malignant lymphoma Myelodysplastic syndrome Colorectal Neoplasms Juvenile myelomonocytic leukemia Noonan syndrome 6 RAS-associated autoimmune leukoproliferative disorder not provided |
Variation | info |
---|
Gene |
NRAS |
CLNDBN |
Neoplasm Malignant melanoma Multiple myeloma Malignant melanoma of skin Medulloblastoma Acute myeloid leukemia Adenocarcinoma of stomach Transitional cell carcinoma of the bladder Malignant lymphoma, non-Hodgkin Myelodysplastic syndrome Colorectal Neoplasms Juvenile myelomonocytic leukemia Noonan syndrome 6 RAS-associated autoimmune leukoproliferative disorder not provided |
Reversed |
1 |
HGVS |
NC_000001.10:g.115258744C>A; NC_000001.10:g.115258744C>G; NC_000001.10:g.115258744C>T |
CLNSRC |
OMIM Allelic Variant UniProtKB (protein) |
CLNACC |
RCV000417850.1, RCV000423218.1, RCV000424444.1, RCV000425977.1, RCV000430805.1, RCV000432522.1, RCV000435607.1, RCV000436237.1, RCV000437557.1, RCV000444067.1, RCV000445025.1, RCV000420759.1, RCV000014915.26, RCV000022690.25, RCV000144962.2, RCV000157672.1, RCV000421229.1, RCV000421906.1, RCV000422699.1, RCV000430350.1, RCV000431020.1, RCV000431528.1, RCV000433031.1, RCV000440357.1, RCV000440593.1, RCV000442419.1, |