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
40101 BAA01g25490 A01 13850701 G A downstream_gene_variant MODIFIER c.*1826C>T| S203
40102 BAA01g25490 A01 13851146 G A downstream_gene_variant MODIFIER c.*1381C>T| S217
40103 BAA01g25490 A01 13851396 C T downstream_gene_variant MODIFIER c.*1131G>A| S167
40104 BAA01g25490 A01 13851755 G A downstream_gene_variant MODIFIER c.*772C>T| S262
40105 BAA01g25490 A01 13851830 G A downstream_gene_variant MODIFIER c.*697C>T| S156
40106 BAA01g25490 A01 13852936 C T missense_variant MODERATE c.641G>A|p.Ser214Asn S280
40107 BAA01g25490 A01 13853501 C T intron_variant MODIFIER c.412-249G>A| S136
40108 BAA01g25490 A01 13853932 G A missense_variant MODERATE c.335C>T|p.Ala112Val S12
40109 BAA01g25490 A01 13854952 G A synonymous_variant LOW c.111C>T|p.Cys37Cys S91
40110 BAA01g25490 A01 13854958 A C missense_variant MODERATE c.105T>G|p.Ser35Arg S147
S91
40111 BAA01g25490 A01 13854961 G A synonymous_variant LOW c.102C>T|p.Asp34Asp S147
S91
40112 BAA01g25490 A01 13854979 A G synonymous_variant LOW c.84T>C|p.Leu28Leu S147
S91
40113 BAA01g25490 A01 13854982 C T synonymous_variant LOW c.81G>A|p.Gln27Gln S147
S15
S91
40114 BAA01g25490 A01 13854989 T G missense_variant MODERATE c.74A>C|p.Asp25Ala S147
S91
40115 BAA01g25490 A01 13854996 G A synonymous_variant LOW c.67C>T|p.Leu23Leu S147
S91
40116 BAA01g25490 A01 13855000 C T synonymous_variant LOW c.63G>A|p.Ala21Ala S147
S91
40117 BAA01g25490 A01 13855004 C T missense_variant MODERATE c.59G>A|p.Arg20His S147
S91
40118 BAA01g25490 A01 13858205 C T upstream_gene_variant MODIFIER c.-3143G>A| S88
40119 BAA01g25490 A01 13858862 C T upstream_gene_variant MODIFIER c.-3800G>A| S250
40120 BAA01g25490 A01 13859287 C T upstream_gene_variant MODIFIER c.-4225G>A| S242
40121 BAA01g25490 A01 13859317 G A upstream_gene_variant MODIFIER c.-4255C>T| S138
40122 BAA01g25490 A01 13859550 C T upstream_gene_variant MODIFIER c.-4488G>A| S218
40123 BAA01g25490 A01 13859763 G A upstream_gene_variant MODIFIER c.-4701C>T| S7
40124 BAA01g25490 A01 13859824 G A upstream_gene_variant MODIFIER c.-4762C>T| S72
S78
40125 BAA01g25490-BAA01g25500 A01 13860173 G A intergenic_region MODIFIER n.13860173G>A| S59