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
195051 BAA02g28350 A02 15920827 G A upstream_gene_variant MODIFIER c.-3636C>T| S280
195052 BAA02g28350 A02 15921745 C T upstream_gene_variant MODIFIER c.-4554G>A| S231
195053 BAA02g28360 A02 15922575 G A missense_variant MODERATE c.377G>A|p.Arg126Lys S302
195054 BAA02g28360 A02 15923039 G A splice_region_variant&synonymous_variant LOW c.627G>A|p.Ala209Ala S35
195055 BAA02g28360 A02 15923477 C T intron_variant MODIFIER c.1006+59C>T| S2
195056 BAA02g28360 A02 15923583 C T missense_variant MODERATE c.1030C>T|p.Pro344Ser S276
195057 BAA02g28360 A02 15923656 C T missense_variant MODERATE c.1103C>T|p.Ser368Phe S81
195058 BAA02g28360 A02 15924671 G A missense_variant MODERATE c.1624G>A|p.Glu542Lys S161
195059 BAA02g28360 A02 15924725 G A intron_variant MODIFIER c.1653+25G>A| S197
195060 BAA02g28360 A02 15926868 G A missense_variant MODERATE c.2848G>A|p.Gly950Arg S169
195061 BAA02g28360 A02 15927219 A G intron_variant MODIFIER c.3028-11A>G| S268
195062 BAA02g28360 A02 15927409 C T splice_region_variant&intron_variant LOW c.3130-3C>T| S162
195063 BAA02g28360 A02 15928177 C T synonymous_variant LOW c.3615C>T|p.Ser1205Ser S39
195064 BAA02g28360 A02 15928194 C T splice_region_variant&intron_variant LOW c.3624+8C>T| S95
195065 BAA02g28360 A02 15928547 G A missense_variant MODERATE c.3760G>A|p.Glu1254Lys S272
195066 BAA02g28360 A02 15928718 C T missense_variant MODERATE c.3848C>T|p.Thr1283Ile S260
195067 BAA02g28360 A02 15928950 G A synonymous_variant LOW c.3993G>A|p.Lys1331Lys S126
195068 BAA02g28360 A02 15929010 C T synonymous_variant LOW c.4053C>T|p.Gly1351Gly S87
195069 BAA02g28360 A02 15929088 C T intron_variant MODIFIER c.4118+13C>T| S193
195070 BAA02g28360 A02 15929166 C T intron_variant MODIFIER c.4118+91C>T| S179
195071 BAA02g28360 A02 15930222 C T missense_variant MODERATE c.4390C>T|p.Leu1464Phe S185
195072 BAA02g28360 A02 15930893 C T missense_variant MODERATE c.4736C>T|p.Ala1579Val S293
195073 BAA02g28360 A02 15931169 C T synonymous_variant LOW c.4933C>T|p.Leu1645Leu S77
S82
195074 BAA02g28360 A02 15931717 G A intron_variant MODIFIER c.5112+10G>A| S263
195075 BAA02g28360 A02 15932552 C T intron_variant MODIFIER c.5365-87C>T| S15
S3