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
127851 BAA10g16210 A10 16147077 C T missense_variant MODERATE c.80G>A|p.Gly27Asp S116
127852 BAA10g16220 A10 16148472 G A missense_variant MODERATE c.589C>T|p.Leu197Phe S287
127853 BAA10g16210 A10 16149350 G A upstream_gene_variant MODIFIER c.-2194C>T| S75
S81
127854 BAA10g16210 A10 16151104 G A upstream_gene_variant MODIFIER c.-3948C>T| S255
127855 BAA10g16240 A10 16152074 G A missense_variant MODERATE c.445C>T|p.His149Tyr S63
127856 BAA10g16240 A10 16152321 G A synonymous_variant LOW c.198C>T|p.Asp66Asp S1
S90
127857 BAA10g16240 A10 16152463 G A missense_variant MODERATE c.56C>T|p.Ser19Phe S111
127858 BAA10g16220 A10 16154119 C T upstream_gene_variant MODIFIER c.-4926G>A| S189
127859 BAA10g16240 A10 16154477 C T upstream_gene_variant MODIFIER c.-1959G>A| S275
127860 BAA10g16240 A10 16155027 G A upstream_gene_variant MODIFIER c.-2509C>T| S75
S81
127861 BAA10g16240 A10 16155082 C T upstream_gene_variant MODIFIER c.-2564G>A| S60
127862 BAA10g16240 A10 16155865 G A upstream_gene_variant MODIFIER c.-3347C>T| S171
127863 BAA10g16240 A10 16156434 G T upstream_gene_variant MODIFIER c.-3916C>A| S259
127864 BAA10g16250 A10 16157957 G A upstream_gene_variant MODIFIER c.-2191C>T| S4
127865 BAA10g16260 A10 16159309 G A missense_variant MODERATE c.2669C>T|p.Ser890Phe S192
127866 BAA10g16250 A10 16159414 G A upstream_gene_variant MODIFIER c.-3648C>T| S252
127867 BAA10g16260 A10 16159659 G A synonymous_variant LOW c.2394C>T|p.Val798Val S105
S106
127868 BAA10g16260 A10 16159855 G A missense_variant MODERATE c.2279C>T|p.Thr760Ile S257
127869 BAA10g16260 A10 16159952 G A splice_region_variant&intron_variant LOW c.2185-3C>T| S219
S72
127870 BAA10g16260 A10 16161063 G A intron_variant MODIFIER c.1626-41C>T| S15
S3
127871 BAA10g16260 A10 16161903 G A synonymous_variant LOW c.1323C>T|p.Ile441Ile S159
S243
127872 BAA10g16260 A10 16162001 C T missense_variant MODERATE c.1225G>A|p.Gly409Ser S110
127873 BAA10g16260 A10 16163543 C T intron_variant MODIFIER c.637-156G>A| S108
127874 BAA10g16260 A10 16164724 G A synonymous_variant LOW c.150C>T|p.Ala50Ala S62
127875 BAA10g16260 A10 16166103 C T upstream_gene_variant MODIFIER c.-1090G>A| S197