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
104501 BAA10g08000 A10 5113061 G A missense_variant MODERATE c.335C>T|p.Pro112Leu S3
104502 BAA10g08000 A10 5113526 G A upstream_gene_variant MODIFIER c.-131C>T| S303
104503 BAA10g08000 A10 5114502 C T upstream_gene_variant MODIFIER c.-1107G>A| S247
104504 BAA10g08000 A10 5114534 G A upstream_gene_variant MODIFIER c.-1139C>T| S236
104505 BAA10g08000 A10 5114649 G A upstream_gene_variant MODIFIER c.-1254C>T| S236
104506 BAA10g08000 A10 5115066 G A upstream_gene_variant MODIFIER c.-1671C>T| S283
104507 BAA10g08000 A10 5116886 C T upstream_gene_variant MODIFIER c.-3491G>A| S176
104508 BAA10g08000 A10 5116897 C T upstream_gene_variant MODIFIER c.-3502G>A| S98
104509 BAA10g08000 A10 5117109 G A upstream_gene_variant MODIFIER c.-3714C>T| S174
S216
S241
S265
S39
104510 BAA10g08000 A10 5117493 C T upstream_gene_variant MODIFIER c.-4098G>A| S269
104511 BAA10g08000 A10 5117918 G A upstream_gene_variant MODIFIER c.-4523C>T| S158
104512 BAA10g08000-BAA10g08010 A10 5118686 C T intergenic_region MODIFIER n.5118686C>T| S233
104513 BAA10g08010 A10 5118976 C T downstream_gene_variant MODIFIER c.*4753G>A| S139
104514 BAA10g08010 A10 5119277 G A downstream_gene_variant MODIFIER c.*4452C>T| S151
S263
104515 BAA10g08010 A10 5119956 C T downstream_gene_variant MODIFIER c.*3773G>A| S282
104516 BAA10g08010 A10 5120448 G A downstream_gene_variant MODIFIER c.*3281C>T| S245
104517 BAA10g08010 A10 5120735 G A downstream_gene_variant MODIFIER c.*2994C>T| S68
104518 BAA10g08010 A10 5120785 G A downstream_gene_variant MODIFIER c.*2944C>T| S136
104519 BAA10g08010 A10 5120997 G A downstream_gene_variant MODIFIER c.*2732C>T| S66
104520 BAA10g08010 A10 5121306 G A downstream_gene_variant MODIFIER c.*2423C>T| S125
104521 BAA10g08010 A10 5121355 C T downstream_gene_variant MODIFIER c.*2374G>A| S6
104522 BAA10g08010 A10 5121359 C T downstream_gene_variant MODIFIER c.*2370G>A| S199
104523 BAA10g08010 A10 5121907 G A downstream_gene_variant MODIFIER c.*1822C>T| S69
104524 BAA10g08010 A10 5122170 C T downstream_gene_variant MODIFIER c.*1559G>A| S9
104525 BAA10g08010 A10 5122543 G A downstream_gene_variant MODIFIER c.*1186C>T| S186