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
118251 BAA10g10920 A10 12653261 C T downstream_gene_variant MODIFIER c.*1751C>T| S190
118252 BAA10g10930 A10 12653416 G A missense_variant MODERATE c.865C>T|p.Pro289Ser S66
118253 BAA10g10920 A10 12655130 G A downstream_gene_variant MODIFIER c.*3620G>A| S288
118254 BAA10g10920 A10 12655363 C T downstream_gene_variant MODIFIER c.*3853C>T| S38
118255 BAA10g10930 A10 12656425 G A upstream_gene_variant MODIFIER c.-802C>T| S288
118256 BAA10g10930 A10 12656975 G A upstream_gene_variant MODIFIER c.-1352C>T| S184
118257 BAA10g10930 A10 12657658 C T upstream_gene_variant MODIFIER c.-2035G>A| S89
118258 BAA10g10930 A10 12658283 G A upstream_gene_variant MODIFIER c.-2660C>T| S257
S262
S263
118259 BAA10g10930 A10 12659658 C T upstream_gene_variant MODIFIER c.-4035G>A| S121
118260 BAA10g10930 A10 12659953 C T upstream_gene_variant MODIFIER c.-4330G>A| S181
118261 BAA10g10940 A10 12661470 C T downstream_gene_variant MODIFIER c.*4544G>A| S301
S304
118262 BAA10g10940 A10 12663369 G A downstream_gene_variant MODIFIER c.*2645C>T| S157
S166
S167
S236
S262
118263 BAA10g10940 A10 12663508 C T downstream_gene_variant MODIFIER c.*2506G>A| S272
118264 BAA10g10940 A10 12663537 C T downstream_gene_variant MODIFIER c.*2477G>A| S142
118265 BAA10g10940 A10 12663971 G T downstream_gene_variant MODIFIER c.*2043C>A| S23
118266 BAA10g10940 A10 12664046 G A downstream_gene_variant MODIFIER c.*1968C>T| S215
118267 BAA10g10940 A10 12664185 C T downstream_gene_variant MODIFIER c.*1829G>A| S123
118268 BAA10g10940 A10 12665351 C T downstream_gene_variant MODIFIER c.*663G>A| S247
118269 BAA10g10940 A10 12665654 G A downstream_gene_variant MODIFIER c.*360C>T| S265
118270 BAA10g10940 A10 12666625 G A synonymous_variant LOW c.2100C>T|p.Asp700Asp S112
118271 BAA10g10940 A10 12667459 C T synonymous_variant LOW c.1350G>A|p.Glu450Glu S201
118272 BAA10g10940 A10 12667496 G A missense_variant MODERATE c.1313C>T|p.Ser438Phe S179
118273 BAA10g10940 A10 12667907 G A synonymous_variant LOW c.1029C>T|p.Phe343Phe S151
S263
118274 BAA10g10940 A10 12669420 T A intron_variant MODIFIER c.216-56A>T| S121
118275 BAA10g10940 A10 12670036 G A intron_variant MODIFIER c.215+284C>T| S35