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
172501 BAA02g16270 A02 7938029 C T upstream_gene_variant MODIFIER c.-3512G>A| S97
172502 BAA02g16270 A02 7938471 C T upstream_gene_variant MODIFIER c.-3954G>A| S302
172503 BAA02g16280 A02 7938863 G A missense_variant MODERATE c.169G>A|p.Ala57Thr S297
172504 BAA02g16290 A02 7940374 C A upstream_gene_variant MODIFIER c.-3307C>A| S304
172505 BAA02g16290 A02 7940713 C T upstream_gene_variant MODIFIER c.-2968C>T| S308
172506 BAA02g16290 A02 7941849 C T upstream_gene_variant MODIFIER c.-1832C>T| S120
172507 BAA02g16290 A02 7941901 G A upstream_gene_variant MODIFIER c.-1780G>A| S202
172508 BAA02g16290 A02 7942635 C T upstream_gene_variant MODIFIER c.-1046C>T| S116
172509 BAA02g16290 A02 7943577 C T upstream_gene_variant MODIFIER c.-104C>T| S84
S93
172510 BAA02g16290 A02 7944396 C T downstream_gene_variant MODIFIER c.*366C>T| S78
S83
172511 BAA02g16300 A02 7945430 C T missense_variant MODERATE c.434G>A|p.Ser145Asn S262
172512 BAA02g16300 A02 7945695 C T missense_variant MODERATE c.169G>A|p.Ala57Thr S135
172513 BAA02g16310 A02 7945909 C T synonymous_variant LOW c.546G>A|p.Gly182Gly S112
172514 BAA02g16310 A02 7945948 G A synonymous_variant LOW c.507C>T|p.Phe169Phe S17
172515 BAA02g16310 A02 7946018 G A missense_variant MODERATE c.437C>T|p.Ala146Val S125
172516 BAA02g16310 A02 7946080 G A synonymous_variant LOW c.375C>T|p.Ser125Ser S57
172517 BAA02g16310 A02 7946119 G A synonymous_variant LOW c.336C>T|p.Gly112Gly S235
172518 BAA02g16310 A02 7946223 G A missense_variant MODERATE c.232C>T|p.Leu78Phe S153
S213
172519 BAA02g16300 A02 7947173 C T upstream_gene_variant MODIFIER c.-1310G>A| S165
172520 BAA02g16300 A02 7949780 T C upstream_gene_variant MODIFIER c.-3917A>G| S98
172521 BAA02g16310 A02 7951289 C T upstream_gene_variant MODIFIER c.-4732G>A| S293
172522 BAA02g16320 A02 7956432 G A upstream_gene_variant MODIFIER c.-4064G>A| S298
172523 BAA02g16320 A02 7957260 T G upstream_gene_variant MODIFIER c.-3236T>G| S299
172524 BAA02g16320 A02 7957389 G A upstream_gene_variant MODIFIER c.-3107G>A| S188
172525 BAA02g16320 A02 7959937 G A upstream_gene_variant MODIFIER c.-559G>A| S125