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
120301 BAA10g11770 A10 13360634 G A downstream_gene_variant MODIFIER c.*2306G>A| S80
120302 BAA10g11770 A10 13360788 C T downstream_gene_variant MODIFIER c.*2460C>T| S131
120303 BAA10g11770 A10 13362516 C T downstream_gene_variant MODIFIER c.*4188C>T| S242
120304 BAA10g11770 A10 13363147 C T downstream_gene_variant MODIFIER c.*4819C>T| S247
120305 BAA10g11780 A10 13363726 C T downstream_gene_variant MODIFIER c.*4490C>T| S128
120306 BAA10g11780 A10 13363913 C T downstream_gene_variant MODIFIER c.*4677C>T| S247
120307 BAA10g11790 A10 13364111 C T upstream_gene_variant MODIFIER c.-4804C>T| S143
120308 BAA10g11790 A10 13365217 C T upstream_gene_variant MODIFIER c.-3698C>T| S166
120309 BAA10g11790 A10 13365824 T G upstream_gene_variant MODIFIER c.-3091T>G| S127
S14
S151
S165
S295
S308
S4
S45
S53
120310 BAA10g11790 A10 13367862 C T upstream_gene_variant MODIFIER c.-1053C>T| S169
120311 BAA10g11800 A10 13369290 C T upstream_gene_variant MODIFIER c.-2517C>T| S10
120312 BAA10g11800 A10 13369609 C T upstream_gene_variant MODIFIER c.-2198C>T| S224
120313 BAA10g11790 A10 13369845 G A splice_acceptor_variant&intron_variant HIGH c.312-1G>A| S45
120314 BAA10g11790 A10 13370035 G A missense_variant MODERATE c.501G>A|p.Met167Ile S278
120315 BAA10g11800 A10 13371372 C T upstream_gene_variant MODIFIER c.-435C>T| S305
120316 BAA10g11800 A10 13372323 G A missense_variant MODERATE c.418G>A|p.Ala140Thr S228
120317 BAA10g11800 A10 13373112 G A missense_variant MODERATE c.739G>A|p.Ala247Thr S296
120318 BAA10g11800 A10 13374345 G A missense_variant MODERATE c.1369G>A|p.Glu457Lys S223
120319 BAA10g11810 A10 13375612 C T upstream_gene_variant MODIFIER c.-303C>T| S239
120320 BAA10g11810 A10 13376162 C T missense_variant MODERATE c.248C>T|p.Ser83Leu S56
120321 BAA10g11810 A10 13376229 C T synonymous_variant LOW c.315C>T|p.Ser105Ser S116
120322 BAA10g11810 A10 13377432 G A missense_variant MODERATE c.889G>A|p.Glu297Lys S219
120323 BAA10g11810 A10 13381821 G A downstream_gene_variant MODIFIER c.*4025G>A| S65
120324 BAA10g11810 A10 13381910 G A downstream_gene_variant MODIFIER c.*4114G>A| S66
120325 BAA10g11810-BAA10g11820 A10 13383286 C T intergenic_region MODIFIER n.13383286C>T| S25