KRAS Chromosome 12

KRAS proto-oncogene, GTPase
81 variants 81 Health Risk

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What This Gene Does
This gene, a Kirsten ras oncogene homolog from the mammalian ras gene family, encodes a protein that is a member of the small GTPase superfamily. A single amino acid substitution is responsible for an activating mutation. The transforming protein that results is implicated in various malignancies, including lung adenocarcinoma, mucinous adenoma, ductal carcinoma of the pancreas and colorectal carcinoma. Alternative splicing leads to variants encoding two isoforms that differ in the C-terminal region. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
RAS type GTPase family
Locus Type
gene with protein product
Location
12p12.1
Ensembl
ENSG00000133703
Associated Conditions (89)
Noonan syndrome
RASopathy
12 conditions
Noonan syndrome 3
Non-small cell lung carcinoma
Cerebral arteriovenous malformation
Vascular malformation
Juvenile myelomonocytic leukemia
Cardiovascular phenotype
Primary intracranial sarcoma
DICER1-mutant
Colorectal cancer
Neoplasm
Pilocytic astrocytoma
Embryonal rhabdomyosarcoma
Carcinoma of pancreas
KRAS-related disorder
Cardio-facio-cutaneous syndrome
Acute myeloid leukemia
Cardiofaciocutaneous syndrome 2
+69 more conditions
Key Variants
All Variants (81)
RSID Category Clinical Significance Conditions
RS1339924833 Health Risk Conflicting classifications of pathogenicity Noonan syndrome, RASopathy, 12 conditions
RS1407509439 Health Risk Conflicting classifications of pathogenicity RASopathy, RASopathy
RS1555192443 Health Risk Conflicting classifications of pathogenicity Noonan syndrome 3, RASopathy, Noonan syndrome 3
RS1592808357 Health Risk Conflicting classifications of pathogenicity Noonan syndrome 3, Noonan syndrome 3
RS17851045 Health Risk Conflicting classifications of pathogenicity Non-small cell lung carcinoma, Cerebral arteriovenous malformation, Vascular malformation
RS200186819 Health Risk Conflicting classifications of pathogenicity Carcinoma of pancreas, Carcinoma of pancreas
RS201170656 Health Risk Conflicting classifications of pathogenicity KRAS-related disorder, KRAS-related disorder
RS373169526 Health Risk Conflicting classifications of pathogenicity Cardio-facio-cutaneous syndrome, Cardiovascular phenotype, Cardio-facio-cutaneous syndrome
RS376520586 Health Risk Conflicting classifications of pathogenicity Acute myeloid leukemia, Cardiofaciocutaneous syndrome 2, Noonan syndrome 3
RS377354475 Health Risk Conflicting classifications of pathogenicity RASopathy, Cardiovascular phenotype, KRAS-related disorder
RS397517476 Health Risk Conflicting classifications of pathogenicity KRAS-related disorder, KRAS-related disorder
RS727503107 Health Risk Conflicting classifications of pathogenicity RASopathy, RASopathy
RS727503108 Health Risk Conflicting classifications of pathogenicity Non-small cell lung carcinoma, Noonan syndrome, Cardio-facio-cutaneous syndrome
RS730880469 Health Risk Conflicting classifications of pathogenicity RASopathy, 12 conditions, RASopathy
RS730880472 Health Risk Conflicting classifications of pathogenicity Neoplasm, Neoplasm
RS751117590 Health Risk Conflicting classifications of pathogenicity RASopathy, Cardiovascular phenotype, KRAS-related disorder
RS757816355 Health Risk Conflicting classifications of pathogenicity RASopathy, 12 conditions, RASopathy
RS758575947 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Cardiovascular phenotype
RS770020203 Health Risk Conflicting classifications of pathogenicity Non-immune hydrops fetalis, Non-immune hydrops fetalis
RS779370636 Health Risk Conflicting classifications of pathogenicity Noonan syndrome 3, RASopathy, Noonan syndrome 3
RS958790148 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, 12 conditions, RASopathy
RS104894366 Health Risk Likely pathogenic Cardiofaciocutaneous syndrome 2, Cardio-facio-cutaneous syndrome, Noonan syndrome
RS1135401776 Health Risk Likely pathogenic Noonan syndrome 3, Noonan syndrome 3, Noonan syndrome 3
RS121913538 Health Risk Likely pathogenic OCULOECTODERMAL SYNDROME, SOMATIC, Encephalocraniocutaneous lipomatosis
RS1555194026 Health Risk Likely pathogenic Noonan syndrome 3, RASopathy, Noonan syndrome 3
RS1555195579 Health Risk Likely pathogenic
RS1592798693 Health Risk Likely pathogenic Noonan syndrome 3, KRAS-related disorder, Noonan syndrome
RS193929331 Health Risk Likely pathogenic Noonan syndrome 3, RASopathy, Noonan syndrome
RS1951405479 Health Risk Likely pathogenic Noonan syndrome, Noonan syndrome
RS1951405809 Health Risk Likely pathogenic Noonan syndrome 3, Noonan syndrome 3
RS202247812 Health Risk Likely pathogenic Noonan syndrome 1, Noonan syndrome 1
RS2135806346 Health Risk Likely pathogenic RASopathy, RASopathy
RS2141481712 Health Risk Likely pathogenic Hereditary breast ovarian cancer syndrome, Hereditary breast ovarian cancer syndrome
RS2141505552 Health Risk Likely pathogenic Thyroid cancer, nonmedullary, 1
RS2141505570 Health Risk Likely pathogenic RASopathy, RASopathy
RS2141506236 Health Risk Likely pathogenic Cardiovascular phenotype, Cardiovascular phenotype
RS2141509652 Health Risk Likely pathogenic Noonan syndrome 3, Noonan syndrome 3
RS2141509708 Health Risk Likely pathogenic Venous malformation, Venous malformation
RS2141509791 Health Risk Likely pathogenic
RS2141509883 Health Risk Likely pathogenic RASopathy, Noonan syndrome 3, RASopathy
RS2548920482 Health Risk Likely pathogenic Vascular malformation, Vascular malformation
RS2548920539 Health Risk Likely pathogenic Cardiofaciocutaneous syndrome 2, Cardiofaciocutaneous syndrome 2
RS387907205 Health Risk Likely pathogenic Cardiofaciocutaneous syndrome 2, Cardio-facio-cutaneous syndrome, Cardiofaciocutaneous syndrome 2
RS397517040 Health Risk Likely pathogenic Non-small cell lung carcinoma, Non-small cell lung carcinoma
RS397517041 Health Risk Likely pathogenic Noonan syndrome, Noonan syndrome
RS727503106 Health Risk Likely pathogenic Non-small cell lung carcinoma, Non-small cell lung carcinoma
RS727503110 Health Risk Likely pathogenic Noonan syndrome, RASopathy, Cardiofaciocutaneous syndrome 2
RS730880470 Health Risk Likely pathogenic
RS730880471 Health Risk Likely pathogenic Autoimmune lymphoproliferative syndrome type 4, Cardiofaciocutaneous syndrome 2, Acute myeloid leukemia
RS104894359 Health Risk Pathogenic Cardiofaciocutaneous syndrome 2, RASopathy, Cardio-facio-cutaneous syndrome
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