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. 2018 Nov 8;47(Database issue):D745–D751. doi: 10.1093/nar/gky1113

Figure 2.

Figure 2.

The variant table for a transcript summarizes the annotation across the transcript for each variant, including the global allele frequency, clinical significance, consequence, allele change as well as five different prediction algorithms to assess the variant impact: SIFT (21), PolyPhen-2 (33), CADD (30), REVEL (29), MetaLR (31) and MutationAssessor (32).