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
90651 BAA10g00730 A10 343550 G A upstream_gene_variant MODIFIER c.-2277G>A| S302
90652 BAA10g00720 A10 343908 G A upstream_gene_variant MODIFIER c.-213C>T| S215
90653 BAA10g00720 A10 344180 C T upstream_gene_variant MODIFIER c.-485G>A| S206
S26
90654 BAA10g00730 A10 346938 G A synonymous_variant LOW c.1038G>A|p.Ala346Ala S208
90655 BAA10g00730 A10 348811 G A downstream_gene_variant MODIFIER c.*1303G>A| S79
S84
90656 BAA10g00730 A10 348991 C T downstream_gene_variant MODIFIER c.*1483C>T| S259
90657 BAA10g00730 A10 349562 C T downstream_gene_variant MODIFIER c.*2054C>T| S286
90658 BAA10g00730 A10 349666 G A downstream_gene_variant MODIFIER c.*2158G>A| S212
90659 BAA10g00730 A10 351074 G A downstream_gene_variant MODIFIER c.*3566G>A| S39
90660 BAA10g00730 A10 352012 C T downstream_gene_variant MODIFIER c.*4504C>T| S47
S95
90661 BAA10g00730 A10 352168 C T downstream_gene_variant MODIFIER c.*4660C>T| S152
90662 BAA10g00750 A10 353255 C T upstream_gene_variant MODIFIER c.-4591C>T| S182
90663 BAA10g00750 A10 353561 C T upstream_gene_variant MODIFIER c.-4285C>T| S87
90664 BAA10g00740 A10 354106 G A missense_variant MODERATE c.634C>T|p.Pro212Ser S140
90665 BAA10g00740 A10 355470 G A upstream_gene_variant MODIFIER c.-731C>T| S293
90666 BAA10g00740 A10 357536 G A upstream_gene_variant MODIFIER c.-2797C>T| S223
90667 BAA10g00750 A10 357914 C T synonymous_variant LOW c.69C>T|p.Ile23Ile S221
90668 BAA10g00760 A10 358420 C T missense_variant MODERATE c.598G>A|p.Gly200Arg S263
90669 BAA10g00760 A10 358954 G A missense_variant MODERATE c.247C>T|p.Pro83Ser S280
90670 BAA10g00760 A10 359960 G A upstream_gene_variant MODIFIER c.-505C>T| S136
90671 BAA10g00760 A10 363196 C T upstream_gene_variant MODIFIER c.-3741G>A| S294
90672 BAA10g00770 A10 363581 C T missense_variant MODERATE c.29C>T|p.Pro10Leu S277
90673 BAA10g00760 A10 364203 T C upstream_gene_variant MODIFIER c.-4748A>G| S138
90674 BAA10g00770 A10 366172 C T intron_variant MODIFIER c.253-1090C>T| S113
90675 BAA10g00770 A10 366730 C T intron_variant MODIFIER c.253-532C>T| S155
S211