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. 2021 Dec 20;14:457. doi: 10.1186/s13104-021-05879-z

Table 1.

Clinically significant information of Deleterious predicted SNPs

SNP ID Chr17 (GRCh37) location Nucleotide change Protein ID Amino acid change Functional Consequence
rs2229839 61559033 C > G ENSP00000290866 P351R Missense variant
rs143507892 61568688 G > A ENSP00000290866 R953Q Coding sequence variant
rs4976 61570937 T > C ENSP00000290866 I1018T Coding sequence variant
rs4977 61571297 T > G ENSP00000397593 F1051V Coding sequence variant
rs12709442 61574215 C > T ENSP00000290866 T1187M Coding sequence variant