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
74501 BAA01g39200 A01 26058874 C T upstream_gene_variant MODIFIER c.-4685G>A| S166
74502 BAA01g39220 A01 26058952 G A missense_variant MODERATE c.437C>T|p.Ala146Val S260
74503 BAA01g39220 A01 26059067 G A missense_variant MODERATE c.322C>T|p.Pro108Ser S306
S308
74504 BAA01g39220 A01 26059218 C T synonymous_variant LOW c.249G>A|p.Leu83Leu S111
74505 BAA01g39210 A01 26059966 C T upstream_gene_variant MODIFIER c.-2699G>A| S261
74506 BAA01g39210 A01 26061146 G A upstream_gene_variant MODIFIER c.-3879C>T| S181
74507 BAA01g39210 A01 26061247 C T upstream_gene_variant MODIFIER c.-3980G>A| S150
74508 BAA01g39210 A01 26061633 C T upstream_gene_variant MODIFIER c.-4366G>A| S272
74509 BAA01g39220 A01 26062519 C T upstream_gene_variant MODIFIER c.-3053G>A| S247
74510 BAA01g39220 A01 26063729 C T upstream_gene_variant MODIFIER c.-4263G>A| S107
74511 BAA01g39250 A01 26064183 C T missense_variant MODERATE c.889C>T|p.Pro297Ser S186
74512 BAA01g39250 A01 26064323 C T synonymous_variant LOW c.945C>T|p.Tyr315Tyr S249
74513 BAA01g39250 A01 26065374 G A missense_variant MODERATE c.1996G>A|p.Ala666Thr S138
74514 BAA01g39250 A01 26065474 C T missense_variant MODERATE c.2096C>T|p.Ala699Val S206
S26
74515 BAA01g39260 A01 26066676 C T missense_variant MODERATE c.52G>A|p.Glu18Lys S239
74516 BAA01g39260 A01 26068652 C T upstream_gene_variant MODIFIER c.-1925G>A| S176
74517 BAA01g39260 A01 26070535 G A upstream_gene_variant MODIFIER c.-3808C>T| S268
74518 BAA01g39280 A01 26071582 G A missense_variant MODERATE c.380G>A|p.Gly127Asp S260
74519 BAA01g39280 A01 26072237 C T missense_variant MODERATE c.835C>T|p.Pro279Ser S165
74520 BAA01g39270 A01 26073598 G A upstream_gene_variant MODIFIER c.-4525C>T| S207
74521 BAA01g39270 A01 26073649 C T upstream_gene_variant MODIFIER c.-4576G>A| S134
74522 BAA01g39270 A01 26073807 G A upstream_gene_variant MODIFIER c.-4734C>T| S297
74523 BAA01g39290 A01 26074733 C T missense_variant MODERATE c.181C>T|p.Pro61Ser S204
74524 BAA01g39300 A01 26075370 G A upstream_gene_variant MODIFIER c.-124G>A| S113
74525 BAA01g39300 A01 26075945 C T synonymous_variant LOW c.174C>T|p.Ile58Ile S104
S52