ClinVar
|
Risk
|
rs121434595(A;A) rs121434595(C;C) rs121434595(T;T) |
Alt
|
rs121434595(A;A) rs121434595(C;C) rs121434595(T;T) |
Reference
|
Rs121434595(G;G) |
Significance |
Pathogenic |
Disease |
Malignant melanoma Carcinoma of colon Giant pigmented hairy nevus Medulloblastoma Transitional cell carcinoma of the bladder Multiple myeloma Adenocarcinoma of stomach Myelodysplastic syndrome Colorectal Neoplasms Malignant lymphoma Acute myeloid leukemia Malignant melanoma of skin Neoplasm of stomach |
Variation | info |
---|
Gene |
NRAS |
CLNDBN |
Malignant melanoma Carcinoma of colon Giant pigmented hairy nevus Medulloblastoma Transitional cell carcinoma of the bladder Multiple myeloma Adenocarcinoma of stomach Myelodysplastic syndrome Colorectal Neoplasms Malignant lymphoma, non-Hodgkin Acute myeloid leukemia Malignant melanoma of skin Neoplasm of stomach |
Reversed |
1 |
HGVS |
NC_000001.10:g.115258745C>A; NC_000001.10:g.115258745C>G; NC_000001.10:g.115258745C>T |
CLNSRC |
OMIM Allelic Variant UniProtKB (protein) |
CLNACC |
RCV000445167.1, RCV000014913.5, RCV000114743.4, RCV000419545.1, RCV000419583.1, RCV000424942.1, RCV000426328.1, RCV000427817.1, RCV000428963.1, RCV000434327.1, RCV000437450.1, RCV000438070.1, RCV000444449.1, RCV000436341.1, |