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ATCDrugsGenesVariantsTargets

ENSG00000097007

ENSG00000097007

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Chromosome
chrUnknown

Unknown

Variants
5

Annotated variants

Drug Interactions
5

Interacting drugs

High Impact
2

High impact variants

Gene Variants
Annotated variants in ENSG00000097007
22_42526694_G/Amissense variantMODERATE0.1500
22_42524947_C/Tsynonymous variantLOW0.0800
22_42522612_A/Gmissense variantHIGH0.0200
22_42523943_T/Cintron variantMODIFIER0.3500
22_42527518_C/Gframeshift variantHIGH0.0010
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