Identification and Provenance fields
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bject ID:
Type ID:Human
Name:
Title: -
Version:1.1
Created: Jan 17, 2018 09:40:17
Created by: Lama Elzohary(lama@gwu.edu)
Modified: -
Modified by: -
Digital Signature:
Verification status:in_progress
Publication_status:Draft
Authors:


Description
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This table contains 13 somatic variants mapping to an NLG position and predicted to cause a loss of the consensus NXS/T motif
at that position in at least three different cancer types. These variants include ONLY those somatic variants
WITHOUT germline variants occurring at the same positions occurring in three or more cancers.



Table Headers
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Column Header		Description
-------------           ------------
UniProtKB_AC:		UniProtKB/Swiss-Prot Accession
Gene Symbol:Recommended symbol that officially represents the gene
Position: position
NetNGlyc_Prediction:Likelihood of actual glycosylation at the sequon, as reported by NetNGlyc
Cancer_Type:Disease ontology ID (DOID) and label of cancers associated with samples containing this variant
Patient_ID:Patient ID from primary source, when available
Mutation_Position:Position of the altered residue
Reference:Reference amino acid
Variation:Altered amino acid resulting from nsSNV
PolyPhen2_Prediction:Functional prediction reported by PolyPhen2 software; can be possibly damaging,
probably damaging or benign


Statistics
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UniProtKB_AC 12
Gene Symbol 12
Position 13
NetNGlyc_Prediction 4
Cancer_Type 13
Patient_ID 13
Mutation_Position 13
Reference 3
Variation 7
PolyPhen2_Prediction 3