Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
92901 BAA10g02490 A10 1206449 G A missense_variant MODERATE c.2083C>T|p.Arg695Cys S277
92902 BAA10g02490 A10 1207316 G A splice_region_variant&synonymous_variant LOW c.1575C>T|p.Leu525Leu S158
92903 BAA10g02490 A10 1207326 G A splice_region_variant&intron_variant LOW c.1573-8C>T| S163
92904 BAA10g02480 A10 1207595 G A downstream_gene_variant MODIFIER c.*1941G>A| S184
92905 BAA10g02490 A10 1207724 C T missense_variant MODERATE c.1346G>A|p.Arg449Lys S288
92906 BAA10g02490 A10 1208727 G A missense_variant MODERATE c.772C>T|p.Pro258Ser S19
92907 BAA10g02490 A10 1209098 T G synonymous_variant LOW c.564A>C|p.Ile188Ile S126
92908 BAA10g02490 A10 1209386 G A missense_variant MODERATE c.377C>T|p.Pro126Leu S38
92909 BAA10g02500 A10 1209828 C T upstream_gene_variant MODIFIER c.-3866C>T| S162
92910 BAA10g02490 A10 1209929 C T missense_variant MODERATE c.101G>A|p.Gly34Glu S173
92911 BAA10g02490 A10 1210759 C T upstream_gene_variant MODIFIER c.-730G>A| S27
92912 BAA10g02490 A10 1211846 G A upstream_gene_variant MODIFIER c.-1817C>T| S197
92913 BAA10g02500 A10 1214704 C T synonymous_variant LOW c.1011C>T|p.Tyr337Tyr S37
92914 BAA10g02500 A10 1214797 C T synonymous_variant LOW c.1104C>T|p.Asp368Asp S263
92915 BAA10g02520 A10 1215205 C T upstream_gene_variant MODIFIER c.-3071C>T| S162
92916 BAA10g02510 A10 1216756 G A missense_variant MODERATE c.221C>T|p.Ala74Val S198
92917 BAA10g02510 A10 1216893 C T synonymous_variant LOW c.84G>A|p.Lys28Lys S294
92918 BAA10g02510 A10 1217521 G A upstream_gene_variant MODIFIER c.-545C>T| S99
92919 BAA10g02530 A10 1219663 C T synonymous_variant LOW c.447G>A|p.Arg149Arg S175
92920 BAA10g02510 A10 1221428 C T upstream_gene_variant MODIFIER c.-4452G>A| S247
92921 BAA10g02510 A10 1221500 G A upstream_gene_variant MODIFIER c.-4524C>T| S228
92922 BAA10g02530 A10 1223056 C T upstream_gene_variant MODIFIER c.-2947G>A| S271
92923 BAA10g02530 A10 1223813 C T upstream_gene_variant MODIFIER c.-3704G>A| S150
92924 BAA10g02540 A10 1225117 C T upstream_gene_variant MODIFIER c.-2779G>A| S169
92925 BAA10g02540 A10 1225863 C T upstream_gene_variant MODIFIER c.-3525G>A| S15
S156
S2
S3
S34