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
182101 BAA02g21240 A02 11381729 C A upstream_gene_variant MODIFIER c.-4401G>T| S134
182102 BAA02g21240 A02 11381820 C T upstream_gene_variant MODIFIER c.-4492G>A| S178
182103 BAA02g21240 A02 11382012 G A upstream_gene_variant MODIFIER c.-4684C>T| S44
182104 BAA02g21250 A02 11383659 G T downstream_gene_variant MODIFIER c.*955C>A| S192
182105 BAA02g21250 A02 11383865 G A downstream_gene_variant MODIFIER c.*749C>T| S5
182106 BAA02g21250 A02 11384622 G A missense_variant MODERATE c.3148C>T|p.Leu1050Phe S57
182107 BAA02g21250 A02 11385127 G A splice_region_variant&intron_variant LOW c.2712+4C>T| S122
182108 BAA02g21250 A02 11386395 C T splice_acceptor_variant&intron_variant HIGH c.1841-1G>A| S38
182109 BAA02g21250 A02 11386637 C T missense_variant MODERATE c.1673G>A|p.Arg558His S18
182110 BAA02g21250 A02 11386707 G A intron_variant MODIFIER c.1641+32C>T| S235
182111 BAA02g21250 A02 11387059 G A synonymous_variant LOW c.1321C>T|p.Leu441Leu S148
S30
S31
182112 BAA02g21250 A02 11388159 C T splice_acceptor_variant&intron_variant HIGH c.882-1G>A| S118
182113 BAA02g21250 A02 11388432 G A missense_variant MODERATE c.767C>T|p.Pro256Leu S103
182114 BAA02g21250 A02 11388546 C T splice_region_variant&intron_variant LOW c.737+8G>A| S221
182115 BAA02g21250 A02 11388643 G A intron_variant MODIFIER c.666-18C>T| S23
182116 BAA02g21250 A02 11389068 C T synonymous_variant LOW c.468G>A|p.Ala156Ala S181
182117 BAA02g21260 A02 11389110 C T downstream_gene_variant MODIFIER c.*4740G>A| S1
S90
182118 BAA02g21250 A02 11391254 G A splice_region_variant&intron_variant LOW c.121+7C>T| S153
S213
182119 BAA02g21250 A02 11391362 G A missense_variant MODERATE c.20C>T|p.Pro7Leu S162
182120 BAA02g21250 A02 11391397 G A upstream_gene_variant MODIFIER c.-16C>T| S103
182121 BAA02g21250 A02 11391551 C T upstream_gene_variant MODIFIER c.-170G>A| S209
182122 BAA02g21250 A02 11393647 C T upstream_gene_variant MODIFIER c.-2266G>A| S286
182123 BAA02g21250 A02 11393663 C T upstream_gene_variant MODIFIER c.-2282G>A| S66
182124 BAA02g21260 A02 11395366 G A missense_variant MODERATE c.2044C>T|p.Leu682Phe S202
182125 BAA02g21250 A02 11395512 G A upstream_gene_variant MODIFIER c.-4131C>T| S225
S73