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
99351 BAA10g06510 A10 3372555 G A missense_variant MODERATE c.701C>T|p.Pro234Leu S169
99352 BAA10g06510 A10 3372881 C T synonymous_variant LOW c.375G>A|p.Lys125Lys S244
99353 BAA10g06510 A10 3372889 G A missense_variant MODERATE c.367C>T|p.Arg123Cys S157
S163
99354 BAA10g06510 A10 3373943 C T intron_variant MODIFIER c.329-1016G>A| S56
99355 BAA10g06510 A10 3373970 C T intron_variant MODIFIER c.329-1043G>A| S210
99356 BAA10g06510 A10 3374113 G A intron_variant MODIFIER c.329-1186C>T| S274
99357 BAA10g06510 A10 3374143 G A intron_variant MODIFIER c.328+1187C>T| S164
99358 BAA10g06510 A10 3374389 C T intron_variant MODIFIER c.328+941G>A| S19
99359 BAA10g06510 A10 3374541 C T intron_variant MODIFIER c.328+789G>A| S23
99360 BAA10g06510 A10 3374606 C T intron_variant MODIFIER c.328+724G>A| S132
S137
S89
99361 BAA10g06510 A10 3374825 G A intron_variant MODIFIER c.328+505C>T| S65
99362 BAA10g06510 A10 3374857 G A intron_variant MODIFIER c.328+473C>T| S112
99363 BAA10g06510 A10 3375352 G A synonymous_variant LOW c.306C>T|p.Ser102Ser S168
99364 BAA10g06510 A10 3376392 G A upstream_gene_variant MODIFIER c.-593C>T| S259
99365 BAA10g06510 A10 3377194 C T upstream_gene_variant MODIFIER c.-1395G>A| S56
99366 BAA10g06510 A10 3377373 G A upstream_gene_variant MODIFIER c.-1574C>T| S59
99367 BAA10g06510 A10 3379225 G A upstream_gene_variant MODIFIER c.-3426C>T| S289
99368 BAA10g06510 A10 3379422 G A upstream_gene_variant MODIFIER c.-3623C>T| S140
99369 BAA10g06520 A10 3385218 G A downstream_gene_variant MODIFIER c.*2830C>T| S51
99370 BAA10g06520 A10 3385307 C T downstream_gene_variant MODIFIER c.*2741G>A| S51
99371 BAA10g06520 A10 3386136 C T downstream_gene_variant MODIFIER c.*1912G>A| S238
99372 BAA10g06520 A10 3387301 C T downstream_gene_variant MODIFIER c.*747G>A| S98
99373 BAA10g06520 A10 3388555 G A synonymous_variant LOW c.591C>T|p.Val197Val S112
99374 BAA10g06520 A10 3388977 G A synonymous_variant LOW c.169C>T|p.Leu57Leu S286
99375 BAA10g06520 A10 3389511 G A upstream_gene_variant MODIFIER c.-366C>T| S18